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Horizon BCBSNJ
Uniform Medical Policy ManualSection:Radiology
Policy Number:155
Effective Date: 03/10/2020
Original Policy Date:02/23/2016
Last Review Date:02/11/2020
Date Published to Web: 04/13/2016
Subject:
Adult Oncology Imaging Policy

Description:
_______________________________________________________________________________________

IMPORTANT NOTE:

The purpose of this policy is to provide general information applicable to the administration of health benefits that Horizon Blue Cross Blue Shield of New Jersey and Horizon Healthcare of New Jersey, Inc. (collectively “Horizon BCBSNJ”) insures or administers. If the member’s contract benefits differ from the medical policy, the contract prevails. Although a service, supply or procedure may be medically necessary, it may be subject to limitations and/or exclusions under a member’s benefit plan. If a service, supply or procedure is not covered and the member proceeds to obtain the service, supply or procedure, the member may be responsible for the cost. Decisions regarding treatment and treatment plans are the responsibility of the physician. This policy is not intended to direct the course of clinical care a physician provides to a member, and it does not replace a physician’s independent professional clinical judgment or duty to exercise special knowledge and skill in the treatment of Horizon BCBSNJ members. Horizon BCBSNJ is not responsible for, does not provide, and does not hold itself out as a provider of medical care. The physician remains responsible for the quality and type of health care services provided to a Horizon BCBSNJ member.

Horizon BCBSNJ medical policies do not constitute medical advice, authorization, certification, approval, explanation of benefits, offer of coverage, contract or guarantee of payment.

__________________________________________________________________________________________________________________________


Abbreviations for Oncology Guidelines
ONC-1: General Guidelines
ONC-2: Primary Central Nervous System Tumors
ONC-3: Squamous Cell Carcinomas of the Head and Neck
ONC-4: Salivary Gland Cancers
ONC-5: Melanomas and Other Skin Cancers
ONC-6: Thyroid Cancer
ONC-7: Small Cell Lung Cancer
ONC-8: Non-Small Cell Lung Cancer
ONC-9: Esophageal Cancer
ONC-10: Other Thoracic Tumors
ONC-11: Breast Cancer
ONC-12: Sarcomas – Bone, Soft Tissue and GIST
ONC-13: Pancreatic Cancer
ONC-14: Upper GI Cancers
ONC-15: Neuroendocrine Cancers and Adrenal Tumors
ONC-16: Colorectal Cancer
ONC-17: Renal Cell Cancer (RCC)
ONC-18: Transitional Cell Cancer
ONC-19: Prostate Cancer
ONC-20: Testicular, Ovarian and Extragonadal Germ Cell Tumors
ONC-21: Ovarian Cancer
ONC-22: Uterine Cancer
ONC-23: Cervical Cancer
ONC-24: Anal Cancer & Cancers of the External Genitalia
ONC-25: Multiple Myeloma and Plasmacytomas
ONC-26: Leukemias, Myelodysplasia and Myeloproliferative Neoplasms
ONC-27: Non-Hodgkin Lymphomas
ONC-28: Hodgkin Lymphoma
ONC-29: Hematopoietic Stem Cell Transplantation
ONC-30: Medical Conditions with Cancer in the Differential Diagnosis
ONC-31: Metastatic Cancer, Carcinoma of Unknown Primary Site, and Other Types of Cancer
ONC-32: Medicare Coverage Policies for PET


Abbreviations for Oncology Guidelines
ACTHadrenocorticotropic hormone
AFPalpha-fetoproteinAPanteroposterior
betaHCGbeta human chorionic gonadotropin
CA 125cancer antigen 125 testCA 19-9cancer antigen 19-9
CA 15-3cancer antigen 15-3CA 27-29cancer antigen 27-29
CBCcomplete blood count
CEAcarcinoembryonic antigenCNScentral nervous system
CRcomplete response
CTAcomputed tomography angiographyDCISductal carcinoma in situ
DLBCLdiffuse large B cell lymphomas
DREdigital rectal examEGDesophagogastroduodenoscopy
ENTear, nose, throatEOTend of therapy
ERCPendoscopic retrograde cholangiopancreatography
ESRerythrocyte sedimentation rateEUAexam under anesthesia
EUSendoscopic ultrasound
FDGfluorodeoxyglucoseFNAfine needle aspiration
FUOfever of unknown origin
GEgastroesophageal GIgastrointestinal
GUgenitourinary
GTRgross total resectionHGhigh grade
HIVhuman immunodeficiency disease
HRPChormone refractory prostate cancerhypermethypermetabolic
IFRTInvolved field radiation therapyinvinvasive
LARlow anterior resectionLCISlobular carcinoma in situ
LDHlactate dehydrogenaseLFTliver function tests
LNDLymph node dissection
MALTmucosa associated lymphoid tissuemaintmaintenance
MENmultiple endocrine neoplasiaMGmyasthenia gravis
MGUSmonoclonal gammopathy of unknown significance
MIBGI-123 metaiodobenzylguanidine scintigraphy
MRAmagnetic resonance angiographyMRImagnetic resonance imaging
MUGA‘multiple gated acquisition’ cardiac nuclear scan
MWAmicrowave ablation
NaFSodium Fluoride
NETNeuroendocrine tumor
NCCN®National Comprehensive Cancer Network
NHLnon-Hodgkin’s lymphomaNPCnasopharyngeal carcinoma
NSABPNational Surgical Adjuvant Breast and Bowel Project
NSAIDSnonsteroidal anti-inflammatory drugs
NSCLCnon-small cell lung cancer
NSGCTnon-seminomatous germ cell tumorPAposteroanterior
PCIprophylactic cranial irradiation
PETpositron emission tomographyCOGChildren’s Oncology Group
PSAprostate specific antigenRFAradiofrequency ablation
RPLNDretroperitoneal lymph node dissection
SqCCasquamous cell carcinomaSCLCsmall cell lung cancer
SIADHsyndrome of inappropriate secretion of antidiuretic hormone
TCCtransitional cell carcinoma
TLHtotal laparoscopic hysterectomy
TNMtumor node metastasis staging system
TSHthyroid-stimulating hormone
TURBTtrans-urethral resection of bladder tumor
VIPomavasoactive intestinal polypeptideWLEwide local incision
WB-MRIwhole body MRI
WMWaldenstrom’s macroglobulinemia WBXRTWhole brain radiation therapy


Policy:
(NOTE: For Medicare Advantage, Medicaid and FIDE-SNP, please refer to the Coverage Sections below for coverage guidance.)

ONC-1: General Guidelines

ONC-1.1: Key Principles
ONC-1.2: Phases of Oncology Imaging and General Phase-Related Considerations
ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology
ONC-1.4: PET Imaging in Oncology
ONC-1.5: Unlisted Procedure Codes in Oncology
ONC-1.6: Predisposition Syndromes

This General Policy section provides an overview of the basic criteria for which oncology imaging may be medically necessary. Details regarding specific conditions or clinical presentations and the associated criteria for which imaging is medically necessary are described in subsequent sections.

ONC-1.1: Key Principles

For this condition imaging is medically necessary based on the following criteria:



    AGE APPROPRIATE GUIDELINES
    Age of Individual
    Appropriate Imaging Guidelines
    ≥ 18 years old at initial diagnosis® Adult Oncology Imaging Guidelines, except where directed otherwise by a specific guideline section
    < 18 years old at initial diagnosis® Pediatric Oncology Imaging Guidelines, except where directed otherwise by a specific guideline section
    15 to 39 years old at initial diagnosis (defined as Adolescent and Young Adult (AYA) oncology individuals)® When unique guidelines for a specific cancer type exist only in either Oncology or Pediatric Oncology, AYA individuals should be imaged according to the guideline section for their specific cancer type, regardless of the individual’s age
    ® When unique guidelines for a specific cancer type exist in both Oncology and Pediatric Oncology, AYA individuals should be imaged according to the age rule in the previous bullet
A recent clinical evaluation (within 60 days) (history and physical examination, laboratory studies, non-advanced imaging studies) or meaningful contact (telephone call, electronic mail or messaging) should be performed prior to considering advanced imaging, unless the member is undergoing guideline-supported scheduled off therapy surveillance evaluation or cancer screening. The clinical evaluation may include a relevant history and physical examination, including biopsy, appropriate laboratory studies, and non-advanced imaging modalities.

Advanced imaging is not indicated for monitoring disease in individuals who choose to not receive standard oncologic therapy, but may be receiving alternative therapies or palliative care and/or hospice. All advanced imaging indicated for initial staging of the specific cancer type can be approved once when the member is considering initiation of a standard therapeutic approach (surgery, chemotherapy, or radiation therapy).

Conventional Imaging (mostly CT, sometimes MRI or bone scan) of the affected area(s) drives much of initial and re-staging and surveillance. PET is not indicated for surveillance imaging unless specifically stated in the diagnosis-specific guideline sections

Routine imaging of brain, spine, neck, chest, abdomen, pelvis, bones, or other body areas is not indicated except where explicitly stated in a diagnosis-specific guideline section, or if one of the following applies:

    ® Known prior disease involving the requested body area
    ® New or worsening symptoms or physical exam findings involving the requested body area (including non-specific findings such as ascites or pleural effusion)
    ® New finding on basic imaging study such as plain x-ray or ultrasound
    ® New finding on adjacent body area CT/MRI study (i.e., pleural effusion observed on CT abdomen)

Brain imaging is performed for signs or symptoms of brain disease
    ® MRI Brain without and with contrast (CPT® 70553) is the recommended study for evaluation of suspected or known brain metastases. If a non-contrast CT head shows suspicious lesion, MRI brain may be obtained to further characterize the lesion
    ® CT without and with contrast (CPT® 70470) can be approved when MRI is contraindicated or not available, or if there is skull bone involvement
    ® Certain malignancies including, but not limited to melanoma, lung cancer and renal cell cancer have indications for brain imaging for asymptomatic members
    ® If stage IV disease is demonstrated elsewhere or if systemic disease progression is noted, refer to disease specific guidelines
    ® Initiation of angiogenesis therapy is not an indication for advanced imaging of the brain in asymptomatic members (Avastin/Bevacizumab; < 3% risk of bleeding and < 1% risk of serious bleeding)

Bone scan supplemented by plain x-rays are the initial imaging modalities for suspected malignant bone pain. For specific imaging indications, see also:
    ® ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology
    ® ONC-31.5: Bone (including Vertebral) Metastases
    ® ONC-31.6: Spinal Cord Compression
    ® ONC-31.7: Carcinoma of Unknown Primary Site

Members receiving cardiotoxic chemotherapy (such as doxorubicin, trastuzumab, pertuzumab, mitoxantrone, etc.) may undergo cardiac evaluation – at baseline and for monitoring while on active therapy.
    ® Horizon BCBSNJ guidelines support using Echocardiography (CPT® 93306, CPT® 93307, or CPT® 93308) rather than MUGA scan for determination of LVED and/or wall motion EXCEPT in one of the circumstances described previously in Adult Cardiac Imaging Policy (Policy #149 in the Radiology Section); CD-3.4: MUGA Study – Cardiac Indications.
    ® The timeframe should be determine by the provider, but no more often than baseline and at every 6 weeks.
    ® May repeat every 4 weeks if cardiotoxic chemotherapeutic drug is withheld for significant left ventricular cardiac dysfunction.
    ® If the LVED is < 50% on echocardiogram than follow up can be done with MUGA at appropriate intervals.
    ® See also: Adult Cardiac Imaging Policy (Policy #149 in the Radiology Section); CD-12.1: Oncologic Indications for Cancer Therapeutics-Related Cardiac Dysfunction (CTRCD)

Adults (≥18 years) with a diagnosis of Li-Fraumeni Syndrome (LFS) may be screened for malignancy with a Whole Body MRI (CPT® 76498) on an annual basis. Annual Brain MRI (CPT® 70553) may be performed as part of Whole Body MRI or as a separate exam. Due to lack of standardization of technique, interpretation, and availability of Whole Body MRI, individuals with LFS are encouraged to participate in clinical trials.

CTA or MRA of a specific anatomic region is indicated when requested for surgical planning when there is suspected vascular proximity to proposed resection margin.

Use of Contrast

CT imaging should be performed with contrast for known or suspected body regions, unless contraindicated.

    ® Shellfish allergy is not a contraindication to contrast. Members with known shellfish allergy do not have contrast reaction any more often than other atopic individuals or members with other food allergies.
    ® For iodinated contrast dye allergy, either CT scans without contrast or MRI scans without and with contrast are indicated.
    ® If CT scanning is considered strongly indicated in a member with known contrast allergy, CT with contrast may be considered to be safely performed following prednisone premedication over a 24 hour period prior to the study.

For members with renal insufficiency which precludes contrast use, CT without contrast appropriate disease-specific areas should be offered. Further imaging (such as MRI) may be indicated if noncontrast CT results are inconclusive.

Severe renal insufficiency, i.e. an eGFR less than 30, is a contraindication for an MRI using a gadolinium-based contrast agent (GBCA) as well. In members with eGFR greater than 40, GBCA administration can be safely performed. GBCA administered to members with acute kidney injury or severe chronic kidney disease can result in a syndrome of nephrogenic systemic fibrosis (NSF), but GBCAs are not considered nephrotoxic at dosages approved for MRI.

Gadolinium deposition has been found in members with normal renal function following the use of gadolinium based contrast agents (GBCAs).

    ® The U.S. Food and Drug Administration (FDA) is investigating the risk of brain deposits following repeated use of GBCAs.
    ® The FDA has noted that, “It is unknown whether these gadolinium deposits are harmful or can lead to adverse health effects.” and have recommended:
      ¡ To reduce the potential for gadolinium accumulation, health care professionals should consider limiting GBCA use to clinical circumstances in which the additional information provided by the contrast is necessary.
      ¡ Health care professionals are also urged to reassess the necessity of repetitive GBCA MRIs in established treatment protocols.

    Radiation Exposure

The use of MRI in place of CT scans to reduce risk of secondary malignancy is not supported by the peer-reviewed literature. Unless otherwise specified in the Guidelines, MRI in place of CT scans for this purpose alone is not indicated. In some instances (i.e., testicular cancer surveillance), MRI may be considered inferior to CT scans.


ONC-1.2: Phases of Oncology Imaging and General Phase-Related Considerations

For this condition imaging is medically necessary based on the following criteria:
Phases of Oncology Imaging
Definition
ScreeningImaging requested for members at increased risk for a particular cancer in the absence of known clinical signs or symptoms
Suspected DiagnosisImaging requested to evaluate a suspicion of cancer, prior to histological confirmation
Initial work-up and StagingImaging requested after biopsy confirmation and prior to starting specific treatment
Treatment response or Interim RestagingImaging performed during active treatment with chemotherapy, endocrine therapy or maintenance therapy
Restaging of locally treated lesionsImaging performed to evaluate primary or metastatic lesions with ablation using radiofrequency, radioactive isotope, microwave or chemotherapy
Restaging / Suspected RecurrenceImaging requested when there is suspicion for progression or recurrence of known cancer based on clinical signs/symptoms, laboratory tests or basic imaging studies
SurveillanceImaging performed in members who are asymptomatic or have chronic stable symptoms, and are not receiving active treatment
General phase-related considerations:

Imaging performed prior to diagnosis should not be repeated unless there is a delay of at least 6 weeks since previous imaging and treatment initiation or there are new or significantly worsening clinical signs or symptoms

Phase
Imaging Timeframe
After definitive local therapy of primary tumor (surgery or radiation therapy)® Follow surveillance guidelines
During adjuvant chemotherapy® Follow surveillance guidelines
After ablative therapy® See disease-specific guidelines
During chemotherapy or immunotherapy for measurable disease® Every 2 cycles (generally every 6 to 8 weeks)
During endocrine/hormonal therapy® Every 3 months
Measurable metastatic disease being monitored off therapy® Every 3 months
Minimal metastatic disease on maintenance therapy® Every 3 months
Surveillance for history of metastatic disease with complete response and being observed off-therapy® Imaging typically not indicated beyond 5 years from completion of treatment for metastatic disease

    ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology

    For this condition imaging is medically necessary based on the following criteria:

    This section does not apply to PET imaging. PET imaging considerations can be found in ONC-1.4: PET Imaging in Oncology

    Bone Scan:

      ® Primarily used for evaluation of bone metastases in members with solid malignancies.
      ® Indications for bone scan in members with history of malignancy include – bone pain, rising tumor markers, elevated alkaline phosphatase or in members with primary bone tumor.
      ® For evaluation of suspected or known bony metastases, CPT® 78306 (Nuclear bone scan whole body), may be approved.
      ® Radiopharmaceutical Localization scan (CPT® 78803) may be approved as an add-on test for further evaluation of a specific area of interest.
      ® CPT® codes 78300 (Nuclear bone scan limited), 78305 (Nuclear bone scan multiple areas) or 78315 do not have any indications in oncology nuclear medicine imaging.

    Octreotide scan:
      ® Specific for low and intermediate grade neuroendocrine tumors which express specific cell surface somatostatin receptors. See cancer specific guidelines for recommended use.
      ® One of the following codes may be approved when Octreotide scan is requested:
        ¡ CPT® 78802 (Radiopharmaceutical localization of tumor whole body single day study)
        ¡ CPT® 78804 (Radiopharmaceutical localization of tumor whole body two or more days)
      ® In addition to one of the above CPT codes, CPT® 78803 (Radiopharmaceutical localization of tumor SPECT) may be approved as an add-on test for further evaluation of a specific area of interest.

    Bone marrow imaging:
      ® This study is rarely performed for evaluation of the entire bone marrow in conditions like myeloproliferative disorders, sickle cell bone infarct or ischemia, avascular necrosis or myeloma
      ® The correct CPT code for this study is CPT® 78104 (Diagnostic Nuclear Medicine Procedures on the Hematopoietic, Reticuloendothelial and Lymphatic System)

    Brain imaging SPECT with Technetium-99m or thallium-201 (CPT® 78803):
      ® Immunocompromised members with mass lesion detected on CT or MRI for differentiation between lymphoma and infection
      ® In distinguishing recurrent brain tumor from radiation necrosis
      ® Immunocompromised members with mass lesion detected on CT or MR for differentiation of lymphoma and infection

    Radiopharmaceutical localization of tumor or distribution of radiopharmaceutical agent(s):
      ® CPT® 78800, CPT® 78801, CPT® 78802, CPT® 78804, CPT® 78803 (SPECT), or CPT® 78830, CPT® 78831, or CPT® 78832 (SPECT/CT)
      ® For evaluation of fever of unknown origin and osteomyelitis
      ® For suspected infections such as infected central lines, grafts or shunts

    Gallium Isotope Scan:
      ® Radiopharmaceutical Localization of tumor (CPT® 78800, CPT® 78801, CPT® 78802, CPT® 78803, or CPT® 78804)
      ® This may be rarely used in place of PET/CT scan when PET/CT scan not available and PET/CT is indicated by guidelines for lymphoma, sarcoma, melanoma or myeloma

    ONC-1.4: PET Imaging in Oncology

    For this condition imaging is medically necessary based on the following criteria:

    NOTE: Some payors have specific restrictions on PET imaging, and those coverage policies may supersede the recommendations for PET imaging in these guidelines.

    CPT codes:

      ® PET imaging in oncology should use PET/CT fusion imaging (CPT® 78815 or CPT® 78816) Unbundling PET/CT imaging into separate PET and diagnostic CT codes is otherwise not supported.
      ® The decision whether to use skull base to mid-femur (“eyes to thighs”) procedure code for PET (CPT® 78812 or CPT® 78815) or whole body PET (CPT® 78813 or CPT® 78816) is addressed in the diagnosis-specific guideline sections.
      ® ‘Limited area’ protocol is done infrequently, but may be considered, and is reported with PET (CPT® 78811) or for PET/CT, (CPT® 78814) and should be forwarded for Medical Director review.

    Radiotracers:
      ® Unless specified otherwise, the term “PET” refers to 18F-FDG-PET and PET/CT fusion studies
      ® Indications for PET/CT imaging using non-FDG radiotracers are listed in diagnosis-specific guidelines. The indications may be as follows:
        ¡ Covered:
          18F-FDG
          68Gallium DOTATATE (NETSPOT®) for low grade neuroendocrine tumors for localization of somatostatin receptor positive neuroendocrine tumors in adult and pediatric population
          11C Choline for prostate cancer
          18F-Fluciclovine (AXUMIN®) for prostate cancer
        ¡ Not covered:
          18F-Na Fluoride PET bone scan
          PET/CT imaging using isotopes other than those specified above

      Most Common Isotopes
      CPT/HCPCS Code
      Code Description
      Brand or common name
      FDA
      approved?
      Code reviewed by eviCore for Horizon?
      A9552
      fluorine-18 (F-18) fluorodeoxyglucose (FDG), diagnostic, per study dose, up to 45 millicuries
      FDG
      Yes, to assess abnormal glucose metabolism
      No
      A9580
      Sodium fluoride f-18, diagnostic, per study dose, up to 30 millicuries
      N/A
      Yes, for bone imaging
      No
      A9587
      Gallium GA-68, dotatate, diagnostic, 0.1 millicurie
      NETSPOT®
      Yes, for localization of somatostatin receptor positive neuroendocrine tumors in adult and pediatric population
      No
      C9461
      Choline C 11, diagnostic, per study dose
      N/A
      Yes, for suspected prostate cancer recurrence
      No
      A9588
      18F-Fluciclovine
      AXUMIN®
      Yes, for suspected prostate cancer recurrence
      No
    Unless specified in diagnosis-specific guideline section PET/CT Imaging is NOT indicated for:
      ® Infection, inflammation, trauma, post-operative healing, granulomatous disease, rheumatological conditions
      ® Concomitantly with separate diagnostic CT studies
      ® Distant or diffuse metastatic disease
      ® Metastatic disease in the central nervous system (CNS)
      ® Lesions less than 8 mm in size
      ® Follow up after localized therapy (i.e. radiofrequency ablation, embolization, stereotactic radiation, etc.)
      ® Rare malignancies, due to lack of available evidence regarding the diagnostic accuracy of PET in rare cancers
      ® Surveillance
        ¡ Serial monitoring of FDG avidity until resolution.
        ¡ PET/CT avidity in a residual mass at the end of planned therapy is not an indication for PET/CT imaging during surveillance.
        ¡ Residual mass that has not changed in size since the last conventional imaging does not justify PET imaging
      ® Unless otherwise specified for a specific cancer type, once PET has been documented to be negative for a given member’s cancer or all PET-avid disease has been surgically resected, PET should not be used for continued disease monitoring or surveillance.

    PET/CT may be indicated if:
      ® Conventional imaging (CT, MRI or bone scan) reveals findings that are inconclusive or negative, with continued suspicion for recurrence
      ® The member is undergoing salvage treatment for a recurrent solid tumor with residual measurable disease on conventional imaging and confirmed repeat negative PET imaging will allow the member to transition from active treatment to surveillance.
      ® PET/CT may be considered prior to biopsy in order to determine a more favorable site for biopsy when a prior biopsy was nondiagnostic or a relatively inaccessible site is contemplated which would require invasive surgical intervention for biopsy attempt.

    PET/CT for rare malignancies is not covered by Horizon BCBSNJ guidelines due to lack of available evidence regarding diagnostic accuracy of PET/CT in the majority of rare cancers. Conventional imaging studies should be used for initial staging and treatment response for these diagnoses. PET/CT can be approved if all of the following apply:
      ® Conventional imaging (CT, MRI or bone scan) reveals equivocal or suspicious findings
      ® No other specific metabolic imaging (MIBG, octreotide, technetium, etc.) is appropriate for the disease type
      ® The submitted clinical information describes a specific decision regarding the member’s care that will be made based on the PET/CT results
      ® These requests will be forwarded for Medical Director review

    Delay PET/CT for at least 12 weeks after completion of radiation treatment, unless required sooner for imminent surgical resection. PET/CT requests < 12 weeks from completion of radiation treatment should be forwarded for Medical Director review.

    PET mammography (PEM, generally reported with CPT® 78811) is considered investigational at this time.


    ONC-1.5: Unlisted Procedure Codes in Oncology

    For this condition imaging is medically necessary based on the following criteria:

    Horizon BCBSNJ authorizes requests for CT or MRI associated with image-directed biopsy or radiation therapy treatment planning for some payors.

    Horizon BCBSNJ does not routinely authorize requests for PET associated with image-directed biopsy or radiation therapy treatment planning.

    There is often no unique procedure code for a service performed solely for treatment planning purposes. AMA instructions in the CPT state that if no specific code exists for a particular service, the service is reported with an unlisted code.

    Advanced imaging being used for radiation therapy treatment planning should not be authorized using any of the diagnostic imaging codes for CT, MRI or PET. In the absence of written payor guidelines, advanced imaging performed in support of radiation therapy treatment planning should be reported with:

      ® CPT® 76498 for Unlisted MRI – when MRI will be used for treatment planning of radiation therapy to be delivered ONLY to the brain, prostate and cervix. The use of this code for radiation treatment planning of any other cancers/body parts not listed above, may be reviewed on a case-by-case basis and should be sent for Medical Director Review.
      ® CPT ® 76497 for Unlisted CT – may NOT be used for radiation treatment planning. CT imaging performed in support of radiation therapy treatment planning is bundled in with the concurrent radiation treatment authorization codes and a separate authorization for treatment planning is not required.
      ® CPT® 78999 for Unlisted procedure, nuclear medicine (PET) – Horizon BCBSNJ does not perform prior authorization for this CPT code for any payor. This code may not be reviewed or offered as an alternative recommendation to the provider.
      ® Imaging associated with image-directed biopsy should be reported with the corresponding interventional codes. See also: General Guidelines for Advanced Imaging Studies (Policy 011 in the Introduction Section); Preface-3: Clinical Information.
      ® For advanced imaging used solely for the purpose of Surgical planning, see General Guidelines for Advanced Imaging Studies (Policy 011 in the Introduction Section); Preface-3: Clinical Information.

    ONC-1.6: Predisposition Syndromes

    For this condition imaging is medically necessary based on the following criteria:

    For predisposition syndrome screening in adult members, see Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-2: Screening Imaging in Cancer Predisposition Syndromes

    References

    1. ACR Committee on Drugs and Contrast Media. ACR Manual on Contrast Media, version 10.3. Reston, VA: American College of Radiology; 2018.
    2. The American College of Radiology. Practice parameter for the performance of skeletal scintigraphy (bone scan). Rev. 2017.
    3. The American College of Radiology. Practice parameter for performing FDG-PET/CT in oncology. Rev. 2016.
    4. The American College of Radiology. Practice parameter for the performance of tumor scintigraphy with gamma cameras). Rev. 2015.
    5. Erdi YE. Limits of tumor detectability in nuclear medicine and PET. Mol Imaging Radionucl Ther. 2012;21(1):23-28. doi:10.4274/Mirt.128.
    6. Hapani S, Sher A, Chu D, Wu S. Increased risk of serious hemorrhage with bevacizumab in cancer patients: a meta-analysis. Oncology. 2010;79(1):27-38. doi:10.1159/000314980.
    7. ACR Appropriateness Criteria. Pretreatment planning of Invasive cancer of Cervix. Rev. 2015.
    8. ACR Appropriateness Criteria. External Beam Radiation therapy treatment planning for clinically localized prostate cancer. Rev. 2016.
    9. Metcalfe P, Liney GP, Holloway L, et al. The potential for an enhanced role for MRI in radiation-therapy treatment planning. Technol Cancer Res Treat. 2013;12(5):429-46. doi:10.7785/tcrt.2012.500342.
    10. National Comprehensive Cancer Network (NCCN) Guidelines Version 3.2019. – January 18, 2019, Genetic/Familial High Risk Assessment: Breast and Ovarian, available at: https://www.nccn.org/professionals/physician_gls/pdf/genetics_screening.pdf. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Genetic/Familial High Risk Assessment: Breast and Ovarian V3.2019. – January 18, 2019 ©. 2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.


    ONC-2: Primary Central Nervous System Tumors

    ONC-2.1: Primary Central Nervous System Tumors – General Considerations
    ONC-2.2: Low Grade Gliomas
    ONC-2.3: High Grade Gliomas
    ONC-2.4: Medulloblastoma and Supratentorial Primitive Neuroectodermal Tumors (sPNET)
    ONC-2.5: Ependymoma
    ONC-2.6: Central Nervous System Germ Cell Tumors
    ONC-2.7: CNS Lymphoma (also known as Microglioma)
    ONC-2.8: Meningiomas (Intracranial and Intraspinal)
    ONC-2.9: Spinal Cord Tumors (Benign and Malignant)
    ONC-2.10: Choroid Plexus Tumors

    This guideline section applies to primary CNS tumors only. For imaging guidelines in metastatic brain cancer, see the appropriate diagnosis-specific section or ONC-31.3: Brain Metastases for imaging guidelines.

    ONC-2.1: General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Primary brain tumors presenting only with uncomplicated headache are very uncommon. Most primary brain tumors present with specific CNS symptoms.

    Histologic confirmation is critical. Therapeutic decisions should not be made on radiographic findings alone, except for the following:

      ® Medically fragile members for whom attempted biopsy carries excess medical risk, as stated in writing by both the attending physician and surgeon.
      ® Brain stem tumors or other sites where the imaging findings are pathognomonic and the risk of permanent neurological damage is excessive with even a limited biopsy attempt.

    For suspected brain tumors in neurofibromatosis, see: Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-2: Screening Imaging in Cancer Predisposition Syndromes

    Rare tumors occurring more commonly in the pediatric population should be imaged according to the imaging guidelines in: Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-4: Pediatric Central Nervous System Tumors


    Indication
    Imaging Study(ies)
    Characterization and follow up of all brain tumors® MRI Brain without and with contrast (CPT® 70553)
    ® CT Head without and with contrast (CPT® 70470) can be approved when MRI is contraindicated or not available, or there is skull bone involvement
    ® CT Head (contrast as requested) can be approved for preoperative planning when requested by the operating surgeon
    Preoperative planning or to clarify inconclusive findings on MRI or CT® MRA Head (CPT® 70544) or CTA Head (CPT® 70496)
    Within 24 to 72 hours following brain tumor surgery® MRI Brain without and with contrast (CPT® 70553)
    Clinical deterioration or development of new neurological features® MRI Brain without and with contrast (CPT® 70553)
    MR Spectroscopy in Brain Tumors (MRS, CPT® 76390)
    NOTE: Some payors have specific restrictions on MR Spectroscopy, and those coverage policies may supersede the recommendations for MRS in these guidelines

    MRS is only supported for use in brain tumors of specified histologies where diagnostic accuracy has been established in peer-reviewed literature

      ® See diagnosis-specific guidelines for MRS indications

    MRS is considered investigational for all other histologies and indications not listed in a diagnosis-specific guideline section. These requests should be forwarded for Medical Director review

    PET Brain Imaging (CPT® 78608 and CPT® 78609)
    NOTE: Some payors have specific restrictions on PET Brain Metabolic Imaging, and those coverage policies may supersede the recommendations for this study in these guidelines.

    PET Brain Metabolic Imaging (CPT® 78608) is only supported for use in brain tumors of specified histologies where diagnostic accuracy has been established in peer-reviewed literature

      ® See diagnosis-specific guidelines for PET indications below.
      ® According to Medicare NCD 220.6.17, FDG-PET may be approved once for initial treatment strategy and three times for subsequent treatment strategy for brain tumors. See: ONC-32.3: Brain PET for details.

    PET Brain metabolic imaging (CPT® 78608) is considered investigational for all other histologies and indications not listed in a diagnosis-specific guideline section and should be forwarded for Medical Director review

    PET Brain perfusion imaging (CPT® 78609) is not indicated in the evaluation or management of primary CNS tumors, and is nationally non-covered by Medicare per NCD 220.6.17.

    Body PET studies (CPT® 78811, CPT® 78812, and CPT® 78813) and fusion PET/CT studies (CPT® 78814, CPT® 78815, or CPT® 78816) are not indicated in the evaluation or management of primary CNS tumors

    ONC-2.2: Low Grade Gliomas

    For this condition imaging is medically necessary based on the following criteria:

    These tumors are defined as having a WHO histologic grade of I or II (out of IV), can occur anywhere in the CNS, and includes the following tumors:
    Pilocytic Astrocytoma
    Fibrillary (or Diffuse) Astrocytoma
    Optic Pathway Gliomas
    Pilomyxoid Astrocytoma
    Oligodendroglioma
    Oligoastrocytoma
    Oligodendrocytoma
    Subependymal Giant Cell Astrocytoma (SEGA)
    Ganglioglioma
    Gangliocytoma
    Dysembryoplastic infantile astrocytoma (DIA)
    Dysembryoplastic infantile ganglioglioma (DIG)
    Dysembryoplastic neuroepithelial tumor (DNT)
    Tectal plate gliomas
    Cervicomedullary gliomas
    Pleomorphic xanthoastrocytoma (PXA)
    Any other glial tumor with a WHO grade of I or II
    Indication
    Imaging Study(ies)
    Initial Staging® MRI Brain without and with contrast (CPT® 70553) if not already done
    ® MRI Spine without and with contrast (Cervical-CPT® 72156, Thoracic-CPT® 72157, Lumbar-CPT® 72158)
    ® MRI Spine with contrast only (Cervical-CPT® 72142, Thoracic-CPT® 72147, Lumbar-CPT® 72149) can be approved if being performed immediately following a contrast-enhanced MRI Brain
    After initial resection or other treatment (XRT, etc.)® MRI Brain without and with contrast (CPT® 70553)
    For members undergoing chemotherapy treatment® MRI Brain without and with contrast (CPT® 70553) every 2 cycles
    ® Members with spinal cord involvement at diagnosis can have MRI without and with contrast of the involved spinal region on the same schedule as MRI brain
    One of the following:
    ® Determine need for biopsy when transformation to high grade glioma is suspected based on clinical symptoms or recent MRI findings
    ® Evaluate a brain lesion of indeterminate nature when the PET findings will be used to determine whether biopsy/resection can be safely postponed
    ® PET Brain metabolic imaging (CPT® 78608)
    One of the following:
    ® Distinguish low grade from high grade gliomas
    ® Evaluate a brain lesion of indeterminate nature when the MRS findings will be used to determine whether biopsy/resection can be safely postponed
    ® Distinguish radiation-induced tumor necrosis from progressive disease within 18 months of completing radiotherapy
    ® MR Spectroscopy (CPT® 76390)
    Surveillance® MRI Brain without and with contrast (CPT® 70553) every 3 months for 2 years, then every 6 months for 3 years, then annually
    ® Members with spinal cord involvement at diagnosis can have MRI spine without and with contrast (Cervical-CPT® 72156, Thoracic-CPT® 72157, Lumbar-CPT® 72158) on the same schedule as MRI Brain


    ONC-2.3: High Grade Gliomas

    For this condition imaging is medically necessary based on the following criteria:

    These tumors are defined as having a WHO histologic grade of III or IV (out of IV can occur anywhere in the CNS (though the majority occur in the brain), and include the following tumors:

    Anaplastic astrocytoma
    Glioblastoma multiforme
    Diffuse intrinsic pontine glioma (DIPG, or “brainstem glioma”)
    Gliomatosis cerebri
    Gliosarcoma
    Anaplastic oligodendroglioma
    Anaplastic ganglioglioma
    Anaplastic mixed glioma
    Anaplastic mixed ganglioneuronal tumors
    Any other glial tumor with a WHO grade of III or IV
    Indication
    Imaging Study(ies)
    Initial Staging
      ® MRI Brain without and with contrast (CPT® 70553) if not already done
      ® MRI Spine without and with contrast (Cervical-CPT® 72156, Thoracic-CPT® 72157, Lumbar-CPT® 72158)
          ¡ MRI Spine with contrast only (Cervical-CPT® 72142, Thoracic-CPT® 72147, Lumbar-CPT® 72149) can be approved if being performed immediately following a contrast-enhanced MRI Brain
    Immediately following partial or complete resection ® MRI Brain without and with (CPT® 70553)
    Immediately following radiation therapy (XRT)® MRI Brain without and with contrast (CPT® 70553) once within 2 to 6 weeks following completion of treatment, and then go to surveillance imaging
    For members undergoing chemotherapy treatment® MRI Brain without and with contrast (CPT® 70553) every 2 cycles
    ® Members with spinal cord involvement at diagnosis can have MRI without and with contrast of the involved spinal region on the same schedule as MRI brain
    One of the following:
    ® Distinguish low grade from high grade gliomas
    ® Evaluate a brain lesion of indeterminate nature when the MRS findings will be used to determine whether biopsy/resection can be safely postponed
    ® Distinguish radiation-induced tumor necrosis from progressive disease within 18 months of completing radiotherapy
    ® MR Spectroscopy (CPT® 76390)
    One of the following:
    ® Distinguish radiation-induced tumor necrosis from progressive disease within 18 months of completing radiotherapy
    ® Evaluate inconclusive MRI findings when the PET findings will be used to determine need for biopsy or change in therapy, including a change from active therapy to surveillance
    ® Evaluate a brain lesion of indeterminate nature when the PET findings will be used to determine whether biopsy/resection can be safely postponed
    ® PET Brain metabolic imaging (CPT® 78608)
    ® PET Brain is not indicated in gliomas occurring in the brain stem due to poor uptake and lack of impact on member outcomes
    Surveillance® MRI Brain without and with contrast (CPT® 70553) every 3 months for 3 years and every 6 months thereafter
    ® Members with spinal cord involvement at diagnosis can have MRI spine without and with contrast (Cervical-CPT® 72156, Thoracic-CPT® 72157, Lumbar-CPT® 72158) on the same schedule as MRI Brain


    ONC-2.4: Medulloblastoma and Supratentorial Primitive Neuroectodermal Tumors (sPNET)

    For this condition imaging is medically necessary based on the following criteria:

    Medulloblastoma and sPNET imaging indications in adult members are identical to those for pediatric members. See Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-4.4: Medulloblastoma (MDB), Supratentorial Primitive Neuroectodermal Tumors (sPNET), and Pineoblastoma for imaging guidelines.



    ONC-2.5: Ependymoma

    For this condition imaging is medically necessary based on the following criteria:

    Ependymoma imaging indications in adult members are identical to those for pediatric members. See Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-4.8: Ependymoma for imaging guidelines.



    ONC-2.6: Central Nervous System Germ Cell Tumors

    For this condition imaging is medically necessary based on the following criteria:

    Central nervous system germ cell tumor imaging indications in adult members are identical to those for pediatric members. See Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-4.7: CNS Germinomas and Non-Germinomatous Germ Cell Tumors (NGGCT) for imaging guidelines.



    ONC-2.7: CNS Lymphoma (also known as Microglioma)

    For this condition imaging is medically necessary based on the following criteria:

    Indication
    Imaging Study
    Initial StagingAll of the following are indicated:
    ® MRI Brain without and with contrast (CPT® 70553)
    ® MRI Cervical spine without and with contrast (CPT® 72156)
    ® MRI Thoracic spine without and with contrast (CPT® 72157)
    ® MRI Lumbar spine without and with contrast (CPT® 72158)
    Extra-neural evaluation to confirm CNS primary

    *Members with CNS Lymphoma that is metastatic should be imaged according to:
    ® ONC-27: Non-Hodgkin Lymphomas for members age ≥ 18 years
    ® Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section);PEDONC-5.3: Pediatric Aggressive Mature B-Cell Non-Hodgkin Lymphomas (NHL) for members age ≤ 17 years

    Any or all of the following are indicated:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® PET/CT (CPT® 78815) can be approved for evaluation of inconclusive findings on CT imaging
    Treatment Response® MRI without and with contrast of all positive disease sites every 2 cycles
    Surveillance® MRI without and with contrast of all positive disease sites every 3 months for 2 years, then every 6 months for 3 years, then annually thereafter

    ONC-2.8: Meningiomas (Intracranial and Intraspinal)

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study(ies)
    Initial Staging of Intracranial MeningiomaAny or all of the following are indicated:
    ® MRI Brain without and with contrast (CPT® 70553)
    ® CT Head (contrast as requested)
    Initial staging of Intraspinal MeningiomaOne of the following:
    ® MRI without and with contrast of appropriate spinal region (Cervical, Thoracic and Lumbar)
    ® CT without and with contrast of the appropriate spinal region (Cervical, Thoracic and Lumbar)
    Treatment Response® MRI without and with contrast of all positive disease sites every 2 cycles
    Surveillance for Grade I (low grade) and Grade II (atypical) meningioma
    (completely resected, partially resected and unresected)
    ® Intracranial Meningioma: MRI Brain without and with contrast (CPT® 70553) at 3, 6, and 12 months, then annually for 5 years
    ® Intraspinal Meningioma: MRI without and with contrast CPT® 72156 (Cervical spine), CPT® 72157 (Thoracic spine), CPT® 72158 (lumbar spine) OR CT without and with contrast CPT® 72127 (Cervical spine), CPT® 72130 (Thoracic spine), CPT® 72133 (Lumbar spine) of the involved spinal level at 3, 6 and 12 months, and then annually for 5 years
    Surveillance for Grade III (malignant or anaplastic) meningioma® Intracranial Meningioma: MRI Brain without and with contrast (CPT® 70553) every 3 months for 3 years, and then every 6 months thereafter
    ® Intraspinal Meningioma: MRI or CT without and with contrast of the involved spinal region every 3 months for 3 years and then every 6 months thereafter


    ONC-2.9: Spinal Cord Tumors (Benign and Malignant)

    For this condition imaging is medically necessary based on the following criteria:

    See also: ONC-2.2: Low Grade Gliomas and ONC-2.3: High Grade Gliomas for imaging guidelines of low grade and high grade gliomas of the spinal cord

    See also: Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-4.9: Malignant Tumors of the Spinal Cord for imaging guidelines for other malignant spinal cord tumors

    See also: Pediatric Peripheral Nerve Disorder Imaging Policy (Policy #168 in the Radiology Section); PEDPN-2.1: Neurofibromatosis 1 and Pediatric Peripheral Nerve Disorder Imaging Policy (Policy #168 in the Radiology Section); PEDPN-2.2: Neurofibromatosis 2 for spinal tumors in members with Neurofibromatosis 1 or 2

    See also: ONC-31.6: Spinal Cord Compression for known secondary malignancy involving the spine/spinal canal/spinal cord


    ONC-2.10: Choroid Plexus Tumors

    For this condition imaging is medically necessary based on the following criteria:

    Choroid Plexus Tumor imaging indications in adult members are identical to those for pediatric members. See Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-4.13: Choroid Plexus Tumors for imaging guidelines.

    References

    1. National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2019 – March 5, 2019 Central Nervous System Cancers, available at: https://www.nccn.org/professionals/physician_gls/pdf/cns.pdf. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Central Nervous System Tumors Cancer V1.2019. – March 5, 2019 ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Brandão LA,Castillo M. Adult brain tumors: clinical applications of magnetic resonance spectroscopy. Magn Reson Imaging Clin N Am. 2016;24(4):781-809. doi:10.1016/j.mric.2016.07.005.
    3. Pasquier D, Bijmolt S, Veninga T, et al. Atypical and malignant meningioma: outcome and prognostic factors in 119 irradiated patients. A multicenter, retrospective study of the Rare Cancer Network. Int J Radiat Oncol Biol Phys. 2008;71(5):1388. doi:10.1016.j.ijrobp.2007.12.020.
    4. Modha A, Gutin PH. Diagnosis and treatment of atypical and anaplastic meningiomas: a review. Neurosurgery. 2005;57(3):538-550.
    5. Horská A, Barker PB. Imaging of brain tumors: MR spectroscopy and metabolic imaging. Neuroimaging Clin N Am. 2010;20(3):293-310. doi:10.1016/j.nic.2010.04.003.
    6. Sundgren PC. MR Spectroscopy in radiation Injury. Am J Neuroradiol. 2009;30(8):1469-1476. doi:10.3174/ajnr.A1580.

    ONC-3: Squamous Cell Carcinomas of the Head and Neck

    ONC-3.0: Squamous Cell Carcinomas of the Head and Neck – General Considerations
    ONC-3.1: Squamous Cell Carcinomas of the Head and Neck – Suspected/Diagnosis
    ONC-3.2: Squamous Cell Carcinomas of the Head and Neck – Initial Work-up/Staging
    ONC-3.3: Squamous Cell Carcinomas of the Head and Neck – Restaging/Recurrence
    ONC-3.4: Squamous Cell Carcinomas of the Head and Neck – Surveillance/Follow-up


    ONC-3.0: Squamous Cell Carcinomas of the Head and Neck – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Members with esthesioneuroblastoma should be imaged according to this guideline section

    For evaluation of squamous cell carcinoma from an unknown primary to the cervical lymph nodes, CT Neck (CPT® 70491) and CT Chest (CPT® 71260) are indicated. CT scans of the abdomen and pelvis are not routinely indicated, unless there are signs/symptoms related to these areas.

    Imaging of the CNS (head, spine) is indicated only to evaluate specific signs or symptoms or if concern for base of skull invasion suggesting spread to those areas

    Stage III/IV disease encompasses any primary tumor larger than 4 cm or documented lymph node positive disease


    ONC-3.1: Squamous Cell Carcinomas of the Head and Neck – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See also: Adult Neck Imaging Policy (Policy #153 in the Radiology Section); NECK-4.1 and Adult Neck Imaging Policy (Policy #153 in the Radiology Section); NECK-5.1 for imaging guidelines for evaluation of suspected malignancy in the neck

    PET may be considered prior to biopsy in order to determine a more favorable site for biopsy when a prior biopsy was nondiagnostic or a relatively inaccessible site is contemplated which would require invasive surgical intervention for biopsy attempt

    ONC-3.2: Squamous Cell Carcinomas of the Head and Neck – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All Stages of Disease® CT Neck with contrast (CPT® 70491) or MRI Orbits/Face/Neck (OFN) without and with contrast (CPT® 70543)
    ® Chest x-ray or CT Chest with contrast (CPT® 71260)
    ® Lymph system imaging (lymphoscintigraphy, CPT® 78195) is indicated for sentinel lymph node evaluation when nodes are not clinically positive
    Nasal cavity and paranasal sinuses (bony erosion or skull base and intracranial involvement)One of the following studies is indicated:
    ® CT Maxillofacial with contrast (CPT® 70487)
    ® CT Neck with contrast (CPT® 70491)
    ® MRI Orbits/Face/Neck without and with contrast (CPT® 70543)
    Nasopharyngeal (NPC) Cancer® MRI Orbits/Face/Neck without and with contrast (CPT® 70543) is the preferred study
        ¡ CT Neck (CPT® 70491) and/or CT Maxillofacial (CPT® 70487) with contrast can be approved if contraindication to MRI
    ® Chest x-ray or CT Chest with contrast (CPT® 71260)
    For any of the following:
    ® Known stage III or IV disease
    ® Prior to start of primary chemoradiotherapy and have not undergone definitive surgical resection
    ® Nasopharyngeal primary site
    ® Inconclusive findings on conventional imaging (CT, MRI)
    ® In order to direct laryngoscopy/exam under anesthesia for biopsy
    ® Pulmonary nodule(s) ≥ 8 mm in size
    ® Cervical lymph node biopsy positive for squamous cell carcinoma and no primary site identified on CT or MRI of neck and chest
    ® Inconclusive findings suggestive of disease outside the head and neck area
    ® PET/CT (CPT® 78815)
    Signs or symptoms of abdominal metastatic disease, including elevated liver function tests ® CT Abdomen with contrast (CPT® 74160)
    Any head and neck cancer with neurological findings or suspicion of skull base invasion ® MRI Brain without and with contrast (CPT® 70553)

    ONC-3.3: Squamous Cell Carcinomas of the Head and Neck – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Following complete resection and/or radical neck dissectionSee (ONC-3.4: Surveillance/Follow-up)
    Following primary chemoradiotherapy for Stage III or IV disease
      ® CT Neck with contrast (CPT® 70491) or MRI Orbits/Face/Neck without and with contrast (CPT® 70543)
      ® PET/CT is indicated (no sooner than 12 weeks post completion XRT) for:
        ¡ Evaluating the need for salvage surgery/radical neck dissection in members with measurable residual disease on physical exam or recent CT or MRI
        ¡ Distinguishing active tumor from radiation fibrosis
    Induction chemotherapy response® CT neck with contrast (CPT® 70491) or MRI Orbits/Face/Neck without and with contrast (CPT® 70543)
    ® PET not indicated to assess response to induction chemotherapy
    Suspected local recurrence ® CT Neck with contrast (CPT® 70491) or MRI Orbits/Face/Neck without and with contrast (CPT® 70543)
    ® CT Chest with contrast (CPT® 71260)
    Biopsy proven local recurrenceEither one of the following:
    ® PET/CT (CPT® 78815)
    OR
    ® CT Neck with contrast (CPT® 70491) or MRI Orbits/Face/Neck without and with contrast (CPT® 70543) AND CT Chest with contrast (CPT® 71260)
    Inconclusive conventional imaging (CT or MRI) ® PET/CT (CPT® 78815)
    If new symptoms or chest previously involved® CT Chest with contrast (CPT® 71260)

    ONC-3.4: Squamous Cell Carcinomas of the Head and Neck – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indications
    Imaging Study
    All stagesOnce within 6 months of completing all treatment:
    ® CT Neck with contrast (CPT® 70491) or MRI Orbits/Face/Neck without and with contrast (CPT® 70543)
    ® CT with contrast of any other involved body area
    After initial post-treatment study, for any of the following:
    ® Nasopharyngeal primary site
    ® Physical exam unable to evaluate primary site for recurrence
    Annually for 3 years:
    ® CT Neck with contrast (CPT® 70491) or MRI Orbits/Face/Neck without and with contrast (CPT® 70543)
    ® CT Chest is not indicated for surveillance. Individuals with smoking history may undergo annual low dose CT cancer screening if criteria are met (See Adult Chest Imaging Policy (Policy #150 in the Radiology Section); CH-34: Lung Screening in the Chest Imaging Guidelines)

    References

    1. Pfister DG, Spencer S, Adelstein D et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – June 28, 2019 Head and Neck Cancers, available at: https://www.nccn.org/professionals/physician_gls/pdf/head-and-neck.pdf. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Head and Neck Cancer V2.2019 – June 28, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Goel R, Moore W, Sumer B, Khan S, Sher D, Subramaniam RM. Clinical practice in PET/CT for the management of head and neck squamous cell cancer. AJR Am J Roentgenol. 2017;209(2):289-303. doi:10.2214/AJR.17.18301.



    ONC-4: Salivary Gland Cancers

    ONC-4.0: Salivary Gland Cancers – General Considerations
    ONC-4.1: Salivary Gland Cancers – Suspected/Diagnosis
    ONC-4.2: Salivary Gland Cancers – Initial Work-up/Staging
    ONC-4.3: Salivary Gland Cancers – Restaging/Recurrence
    ONC-4.4: Salivary Gland Cancers – Surveillance/Follow-up

    ONC-4.0: Salivary Gland Cancers – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Salivary gland tumors may originate within the parotid, submandibular, sublingual or minor salivary glands in the mouth.

    Histological subtypes include mucoepidermoid, acinic, adenocarcinoma, adenoid cystic carcinoma, malignant myoepithelial tumors and squamous cell carcinoma. Lymphoma and metastatic squamous carcinoma can also occur in the parotid gland.

    Over 80% of parotid gland tumors are benign. A bilateral parotid tumor is most likely Warthin’s tumor.

    The role of PET in salivary gland tumors has yet to be established.

    ONC-4.1: Salivary Gland Cancers – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Neck Imaging Policy (Policy #153 in the Radiology Section); NECK-11 and Adult Neck Imaging Policy (Policy #153 in the Radiology Section); NECK-4.1 for evaluation of salivary gland masses, salivary gland stones and neck masses.

    ONC-4.2: Salivary Gland Cancers – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Biopsy-proven malignancy (only if none of these imaging studies has already been done)One of the following can be approved:
    ® MRI Orbits/Face/Neck without and with contrast (CPT® 70543)
    ® CT Neck with contrast (CPT® 70491)
    ® CT Neck without contrast (CPT® 70490)
    Skull base invasion® MRI Brain without and with contrast (CPT® 70553)
    Abnormalities on chest x-ray or if lymphadenopathy in neck® CT Chest with contrast (CPT® 71260)
    Pulmonary nodule(s) ≥ 8mm in size® PET/CT (CPT® 78815)
    ONC-4.3: Salivary Gland Cancers – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Members with unresected disease receiving systemic therapy (chemotherapy)One of the following may be approved every 2 cycles:
    ® CT Neck with contrast (CPT® 70491) and any other sites of disease
    ® MRI Orbits/Face/Neck without and with contrast (CPT® 70543) and any other sites of disease
    Recurrence or progression suspected based on new or worsening signs or symptomsOne of the following may be approved:
    ® CT Neck with contrast (CPT® 70491)
    ® MRI Orbits/Face/Neck without and with contrast (CPT® 70543)

    In addition, for all members:
    ® CT Chest with contrast (CPT® 71260)

    All other members® No routine advanced imaging indicated
    ONC-4.4: Salivary Gland Cancers – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Total surgical resection ® No routine advanced imaging indicated
    Unresectable or partially resected disease, including those treated with XRT® Either CT Neck (CPT® 70491) or MRI Orbits/Face/Neck (CPT® 70543) once within 6 months of completion of treatment

    References

    1. Pfister DG, Spencer S, Adelstein D et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – June 28, 2019 Head and Neck Cancers, available at: https://www.nccn.org/professionals/physician_gls/pdf/head-and-neck.pdf. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Head and Neck Cancer V2.2019 – June 28, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Palacios E, Ellis M, Lam EC, Neitzschman H, Haile M. Pitfalls in imaging the submandibular glands with PET/CT. Ear Nose Throat J. 2015;94(10-11):E37-E39.
    3. Seo YL, Yoon DY, Baek S, et al. Incidental focal FDG uptake in the parotid glands on PET/CT in patients with head and neck malignancy. Eur Radiol. 2015;25(1):171-177. doi:10.1007/s00330-0140339701.
    4. Park HL, Yoo le R, Lee N, et al. The value of F-18 FDG PET for planning treatment and detecting recurrence in malignant salivary gland tumors: comparison with conventional imaging studies. Nucl Med Mol Imaging. 2013;47(4):242-248. doi:10.1007/s13139-013-0222-8.
    5. Bertagna F, Nicolai P, Maroldi R. Diagnostic role of 18F-FDG-PET or PET/CT in salivary gland tumors: a systematic review. Rev Esp Med Nucl Imagen Mol. 2015;34(5):295-302.


    ONC-5 Melanomas and Other Skin Cancers

    ONC-5.0: Melanoma – General Considerations
    ONC-5.1: Melanoma – Suspected/Diagnosis
    ONC-5.2: Melanoma – Initial Work-up/Staging
    ONC-5.3: Melanoma – Restaging/Recurrence
    ONC-5.4: Melanoma – Surveillance/Follow-up
    ONC-5.5: Non-Melanoma Skin Cancers –General Considerations
    ONC-5.6: Non-Melanoma Skin Cancers –Initial Work-up/Staging
    ONC-5.7: Non-Melanoma Skin Cancers –Restaging/Recurrence
    ONC-5.8: Non-Melanoma Skin Cancers – Surveillance/Follow-up
    ONC-5.9: Ocular Melanoma

    ONC-5.0: Melanoma – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Melanomas can metastasize in an unpredictable fashion.

    Primary mucosal melanomas (i.e., gastrointestinal or sinus mucosa) are considered (and should be managed as) Stage III (i.e., node positive) at initial diagnosis.

    ONC-5.1: Melanoma – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All ® Imaging is not indicated until histologic diagnosis is confirmed

    ONC-5.2: Melanoma – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Stage 0 or Ia (in situ or disease < 1 mm)® Routine advanced imaging is not indicated
    ® Stage Ib (≤ 1 mm with ulceration or high mitotic rate)
    ® Stage II (lesions > 1 mm thick, but node negative)
    ® CT with contrast or MRI without and with contrast of specific areas, only if signs or symptoms indicate need for further evaluation
    ® Lymph system imaging (lymphoscintigraphy, CPT® 78195) is indicated for sentinel lymph node (SLN) evaluation
    Any of the following:
    ® Stage III (sentinel node positive, palpable regional nodes)
    ® Stage IV (metastatic)
    ® Mucosal, including lip primary
    ® PET/CT (CPT® 78815 or CPT® 78816)
    OR
    ® CT with contrast of Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177)
    ® CT Neck with contrast (CPT® 70491) is indicated for head or neck primary sites or if palpable lymph nodes are present in the neck
    ® MRI Brain without and with contrast (CPT® 70553)
    ® Primary site of melanoma is unknown and CT Chest and Abdomen/Pelvis are negative® PET/CT (CPT® 78815 or CPT® 78816)

    ONC-5.3: Melanoma – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:

    All recurrences should be confirmed histologically, except when excessive morbidity from a biopsy may occur, such as a biopsy requiring craniotomy.
    Indication
    Imaging Study
    Members receiving chemotherapy, with measurable disease® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast every 2 cycles (commonly every 6 to 8 weeks)
    All in situ recurrences® Restaging imaging is not needed after adequate aggressive local therapy (see Surveillance below)
    Documented or clinically suspected (see top of page regarding biopsy morbidity) recurrence at:
    ® Primary site
    ® In-transit disease
    ® Regional lymph nodes
    ® Metastatic site
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® MRI Brain without and with contrast (CPT® 70553)
    ® PET/CT (CPT® 78815 or CPT® 78816) if inconclusive conventional imaging or isolated metastatic based on results of conventional imaging, initially
    Brain imaging is indicated for:
    ® New discovery of metastatic disease or progression of metastatic disease
    ® Signs or symptoms of CNS disease
    ® If considering Interleukin (IL-2) therapy
    ® MRI Brain without and with contrast (CPT® 70553)

    ONC-5.4: Melanoma – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Stage 0, IA, IB and IIA Melanomas® No routine advanced imaging indicated
    Stage IIB, IIC, IIIA and IIIB Melanomas® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast every 6 months for 5 years
    Stage IIIC and IV Melanomas® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast every 3 months for 3 years, then every 6 months for 2 years
    ® MRI Brain without and with contrast (CPT® 70553) annually for 5 years
    Liver metastases treated with focal therapy® See also: ONC-31.2: Liver Metastases

    ONC-5.5: Non-Melanoma Skin Cancers – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Advanced Imaging is generally not indicated for basal cell and squamous cell skin cancers

    PET/CT scan is not indicated for evaluation of non-melanoma skin cancers unless specified within the guidelines below (e.g. Merkel cell carcinoma)

    Merkel cell carcinoma is an unusual skin cancer with neuroendocrine-like histologic features, which has a high propensity (25% to 33%) for regional lymph node spread and occasionally, metastatic spread to lungs.

    Merkel cell carcinoma may present as a primary cancer or as a skin metastasis from a noncutaneous primary neuroendocrine carcinoma (i.e., small cell lung cancer), therefore conventional imaging is indicated initially to confirm the absence of metastasis prior to considering PET scan.

    ONC-5.6: Non-Melanoma Skin Cancers – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Body area with unexplained signs or symptoms® CT with contrast of that body area
    Perineural invasion or local regional extension (i.e. bone; deep soft tissue) involvement One of the following may be approved of the primary site:
    ® MRI without contrast or without and with contrast
    ® CT (contrast as requested)
    Skin lesion may be a dermal metastasis from distant primary® CT Chest (CPT® 71260) and Abdomen/Pelvis (CPT® 74177) with contrast
    ® PET/CT (CPT® 78815 or 78816) is indicated if conventional imaging (CT or MRI) is unable to identify a primary site
    Squamous cell carcinoma head or neck skin with regional lymphadenopathy® CT Neck (CPT® 70491) and CT Chest (CPT® 71260) with contrast
    Merkel Cell carcinoma® CT Chest (CPT® 71260) and Abdomen/Pelvis (CPT® 74177) with contrast
    ® CT with contrast of other involved body area(s)
    ® PET/CT (CPT® 78815 or 78816) if no metastatic disease identified on conventional imaging
    ® Lymph system imaging (lymphoscintigraphy, CPT® 78195) or sentinel lymph node evaluation
    ® MRI Brain with and without contrast (CPT® 70553)


    ONC-5.7: Non-Melanoma Skin Cancers – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:

    All recurrences should be confirmed histologically, except when excessive morbidity from a biopsy may occur, such as a biopsy requiring craniotomy.
    Indication
    Imaging Study
    Recurrence where planned therapy is more extensive than simple wide local excision® CT with contrast of the primary and recurrent site(s)
    Recurrence of Merkel cell carcinoma® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® MRI Brain without and with contrast (CPT® 70553)
    ® PET/CT if no metastatic disease on any of the previous imaging studies

    ONC-5.8: Non-Melanoma Skin Cancers – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Merkel cell cancer – only if node positive ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast every 6 months for 5 years
    ® Add CT Neck with contrast (CPT® 70491) if known prior neck disease or scalp/facial/neck disease
    All others® Routine advanced imaging for surveillance is not indicated
    ® Imaging indicated only for signs and symptoms of recurrent disease

    ONC-5.9: Ocular Melanoma

    For this condition imaging is medically necessary based on the following criteria:

    General Considerations

    Approximately 95% of ocular melanomas arise from the uvea (iris, ciliary body and choroid) and 5% arise from the conjunctiva or orbit.

    Treatment is directed to the affected eye with systemic therapy reserved only for known metastatic disease.

    The most common site of metastatic disease is the liver.

    Surveillance of the affected eye is with clinical examination only; advanced imaging is supported for surveillance of systemic metastatic disease based on individual risk factors. See Risk categories below for surveillance recommendations.

    Ocular Melanoma Risk Categories
    Low Risk
    Medium Risk
    High Risk
    T1T2 and T3T4
    Class IAClass IBClass 2
    Spindle cell histologyMixed Spindle and Epitheloid cellsEpitheloid cell histology
    No extraoccular extensionNo extraoccular extensionExtraoccular extension present
    No ciliary body involvementNo ciliary body involvementCiliary body involvement present
    Chromosome mutations:
    Disomy 3
    EIF1AZ mutation
    Chromosome mutations:
    SF3B1 mutation
    Chromosome mutations:
    BAP1 mutation
    PRAME mutation
    Monosomy 3
    Gain of chromosome 8q
    Indication
    Imaging Study
    Initial staging Any or all of the following:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® MRI orbits/face/neck without and with contrast (CPT® 70543)
    Restaging/Suspected RecurrenceAny or all of the following:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® MRI orbits/face/neck without and with contrast (CPT® 70543)
    Surveillance: (see Risk Categories Table above)

    ® Low Risk

    ® Medium Risk


    ® High Risk
    ® No routine surveillance imaging

    ® CT Chest with contrast (CPT® 71260) and CT Abdomen with contrast (CPT® 74160) annually for 10 years

    ® CT Chest with contrast (CPT® 71260) and CT Abdomen with contrast (CPT® 74160) every 6 months for 5 years, then annually for 10 years


    References

    1. Coit DG, Thompson JA, Albertini MR, et al, National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – March 12, 2019 Cutaneous Melanoma, available at: https://www.nccn.org/professionals/physician_gls/pdf/melanoma.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Melanoma V2.2019 – March 12, 2019 ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    1. Coit DG, Thompson JA, Albertini MR, et al, National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2018 – March 15, 2018 Uveal Melanoma, available at: https://www.nccn.org/professionals/physician_gls/pdf/uveal.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Melanoma V1.2018 – March 15, 2018 ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org .
    2. Bichakjian CK, Olencki T, Aasi SZ, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – January 18, 2019 Merkel Cell Carcinoma, available at: https://www.nccn.org/professionals/physician_gls/pdf/mcc.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Merkel Cell Carcinoma V2.2019 - June 19, 2019 ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org .
    3. Bichakjian CK, Olencki T, Aasi SZ et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2019 – August 31, 2018 Basal Cell Skin Cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/nmsc.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Basal Cell Skin Cancer V1.2019 – August 31, 2018 ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org .
    4. Bichakjian CK, Olencki T, Aasi SZ, et al, National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – October 23, 2018 Squamous Cell Skin Cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/squamous.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Squamous Cell Skin Cancer V2.2019 – October 23, 2018 ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org .
    5. Schröer-Günther MA, Wolff RF, Westwood ME, et al. F-18-fluoro-2-deoxyglucose positron emission tomography (PET) and PET/computed tomography imaging in primary staging of patients with malignant melanoma: a systematic review. Syst Rev. 2012;1:62. doi:10.1186/2046-4053-1-62.
    6. Xing Y, Bronstein Y, Ross MI, et al. Contemporary diagnostic imaging modalities for the staging and surveillance of melanoma patients: a meta-analysis. J Natl Cancer Inst. 2011;103(2):129-142. doi:10.1093/jnci/djq455.
    7. Rodriguez Rivera AM, Alabbas H, Ramjuan A, Meguerditchian AN. Value of positron emission tomography scan in stage III cutaneous melanoma: a systematic review and meta-analysis. Surg Oncol. 2014;23(1):11-16. doi: 10.1016/j.suronc.2014.01.002.
    8. Nathan P, Cohen V, Coupland S, et al. Uveal melanoma UK national guidelines. European Journal of Cancer. 2015;51(16):2404-2412. doi:10.1016/j.ejca/2015.07.013.

    ONC-6: Thyroid Cancer

    ONC-6.0: Thyroid Cancer – General Considerations
    ONC-6.1: Thyroid Cancer – Suspected/Diagnosis
    ONC-6.2: Thyroid Cancer – Initial Work-up/Staging
    ONC-6.3: Thyroid Cancer – Restaging/Recurrence
    ONC-6.4: Thyroid Cancer – Surveillance/Follow-up

    ONC-6.0: Thyroid Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    PET for initial staging for anaplastic thyroid cancer is currently not recommended before conventional imaging since recommendations for PET are derived from observational studies and clinical trials with other methodological limitations.

    Members with measurable metastatic disease that are RAI refractory may be followed with conventional imaging, PET-CT scan is reserved for inconclusive findings.

    Whole body thyroid nuclear scan is coded with CPT® 78018. If CPT® 78018 is obtained and found to be positive, CPT® 78020 may be approved as an add-on test to evaluate the degree of iodine uptake.

    Single photon emission computed tomography (SPECT) imaging may be performed as needed. SPECT/CT imaging (CPT® 78803) Radiopharmaceutical Localization of Tumor SPECT may complement planar and pinhole imaging and can be approved as an add-on wherever radioiodine scans are indicated.

    ONC-6.1: Thyroid Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Neck Imaging Policy (Policy #153 in the Radiology Section); NECK-8.1: Thyroid Nodule for imaging guidelines for suspected thyroid malignancies

    ONC-6.2: Thyroid Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Follicular, Papillary and
    Hürthle Cell Carcinomas
    Imaging Study
    One of the following:
    ® Fixation suggested by clinical exam and/or ultrasound
    ® Substernal or bulky disease
    ® Disease precluding full ultrasound examination
    One of the following:
    ® MRI Neck without contrast (CPT® 70540)
    ® MRI Neck without and with contrast (CPT® 70543)
    ® CT Neck without contrast (CPT® 70490)
    ® CT Neck with contrast (CPT® 70491) can be approved if contrast study is necessary for complete pre-operative assessment and use of IV contrast will not delay post-operative use of RAI therapy.
    Post-thyroidectomy to assess thyroid remnant and to look for iodine-avid metastases for one of the following:
    ® Extent of thyroid remnant cannot be accurately ascertained from the surgical report or neck ultrasound
    ® When the results may alter the decision to treat
    ® Prior to administration of RAI therapy
    ® Whole body thyroid nuclear scan (CPT® 78018)
    ® The following may be approved as an add-on test:
      ¡ CPT® 78020 to evaluate the degree of iodine uptake
      ¡ SPECT (CPT® 78803), or SPECT/CT Hybrid study (CPT® 78830, 78831, or 78832)
    Skeletal painOne of the following:
    ® Bone scan
      See also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology
    ® Whole body nuclear thyroid scan (CPT® 78018)
    ® The following may be approved as an add-on test:
        ¡ CPT® 78020 to evaluate the degree of iodine uptake
        ¡ SPECT (CPT® 78803), or SPECT/CT Hybrid study (CPT® 78830, 78831, or 78832)
    Suspicious findings on CXR, US, or substernal extension of mass® CT Chest without contrast (CPT® 71250)
    All other members® Routine preoperative advanced imaging is not indicated
    Medullary Thyroid Carcinomas
    Imaging Study
    All members with positive lymph nodes or calcitonin level > 500 pg/mLAny or all of the following:
    ® CT Neck with contrast (CPT® 70491)
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen either with (CPT® 74160) or CT Abdomen without and with contrast (CPT® 74170)
    ® Bone scan see also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology
    Skeletal pain ® Bone scan see also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology
    Inconclusive finding on conventional imaging® PET/CT (CPT® 78815)
    Anaplastic Thyroid Carcinomas
    Imaging Study
    All Any or all of the following:
    ® CT Neck with contrast (CPT® 70491)
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® MRI Brain without and with contrast (CPT® 70553)
    ® Bone scan see also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology
    Skeletal pain ® Bone scan see also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology
    Inconclusive finding on conventional imaging® PET/CT (CPT® 78815 or CPT® 78816)
    ONC-6.3: Thyroid Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Follicular, Papillary and Hürthle Cell Carcinomas
    Imaging Study
    Within 2 weeks (ideally 7 to 10 days) following the administration of Radioactive Iodine therapy dose® Whole body thyroid nuclear scan (CPT® 78018)
    ® The following may be approved as an add-on test:
        ¡ CPT® 78020 to evaluate the degree of iodine uptake
        ¡ SPECT (CPT® 78803), or SPECT/CT Hybrid study (CPT® 78830, 78831, or 78832)
    Any of the following:
    ® Recurrence documented by biopsy
    ® Increasing thyroglobulin level without Thyrogen® stimulation
    ® Thyroglobulin level > 2 ng/mL or higher than previous after Thyrogen® stimulation
    ® Anti-thyroglobulin antibody present
    ® Evidence of residual thyroid tissue on ultrasound or physical exam after thyroidectomy or ablation
    Any or all of the following:
    ® Whole body thyroid nuclear scan (CPT® 78018)
    ® The following may be approved as an add-on test:
      ¡ CPT® 78020 to evaluate the degree of iodine uptake ¡ SPECT (CPT® 78803), or SPECT/CT Hybrid study (CPT® 78830, 78831, or 78832)
    ® CT with contrast of any symptomatic body area
    ® MRI without and with contrast of any symptomatic body area
    Any of the following:
    ® Negative radioiodine scan and rising thyroglobulin level
    ® Inconclusive findings on conventional imaging (including I-131 study)
    ® PET/CT (CPT® 78815)
    Medullary and Anaplastic
    Thyroid Carcinomas
    Imaging Study
    Medullary carcinoma with elevated calcitonin or CEA, or signs or symptoms of recurrence Any or all of the following:
    ® CT Neck with contrast (CPT® 70491)
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen either with (CPT® 74160) or without and with contrast (CPT® 74170)
    ® Bone scan
    See also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology
    Anaplastic carcinoma with signs or symptoms of recurrenceAny or all of the following:
    ® CT Neck with contrast (CPT® 70491)
    ® CT Chest with contrast (CPT® 71260)
    ® Either CT Abdomen/Pelvis with contrast (CPT® 74177) OR MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast
    Inconclusive conventional imaging® PET/CT (CPT® 78815)

    ONC-6.4: Thyroid Cancer – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Follicular, Papillary and
    Hürthle Cell Carcinomas
    Imaging/Diagnostic Study
    All members® Neck ultrasound (CPT® 76536), chest x-ray, and laboratory studies every 6 months for the first year, then annually
    For members with any of the following:
    ® Node positive disease
    ® RAI-avid metastases
    ® Whole body thyroid nuclear scan annually (CPT® 78018)
    ® The following may be approved as an add-on test:
      ¡ CPT® 78020 to evaluate the degree of iodine uptake
      ¡ SPECT (CPT® 78803), or SPECT/CT Hybrid study (CPT® 78830, 78831, or 78832)
    Medullary Carcinomas
    Imaging/Diagnostic Study
    All members® CEA and calcitonin are required for monitoring medullary carcinomas
    ® Routine surveillance imaging is not indicated
    Anaplastic Thyroid Carcinomas
    Imaging Study
    All membersEvery 3 months for 2 years:
    ® CT Neck with contrast (CPT® 70491)
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    References

    1. Haddad RH, Lydiatt WM, Bischoff L, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 3.2018 – December 20, 2018 Thyroid carcinoma, available at: https://www.nccn.org/professionals/physician_gls/pdf/thyroid.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Thyroid carcinoma V3.2018 – December 20, 2018 ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    1. Slough CM, Randolph GW. Workup of well-differentiated thyroid carcinoma. Cancer Control. 2006;13(2):99-105. doi:10.1177/107327480601300203.
    2. Smallridge RC, Ain KB, Asa SL, et al. American Thyroid Association guidelines for management of patients with anaplastic thyroid cancer. Thyroid. 2012;22(11):1104-1139. doi:10.1089/thy.2012.0302.
    3. Wells SA Jr, Asa SL, Dralle H, et al. American Thyroid Association guidelines for the management of medullary thyroid carcinoma. Thyroid. 2015;25(6):567-610. doi:10.1089/thy.2014.0335.
    4. Yeh MW, Bauer AJ, Bernet VA, et al. American Thyroid Association statement on preoperative imaging for thyroid cancer surgery. Thyroid. 2015;25:3-14. doi:10.1089/thy.2014.0096.
    5. Haugen BR, Alexander EK, Bible KB, et al. 2015 American Thyroid Association management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer: the American Thyroid Association guidelines task force on thyroid nodules and differentiated thyroid cancer. Thyroid. 2016;26(1):1-133. doi:10.1089/thy.2015.0020.
    6. Silberstein EB, Alavi A, Balon HR, et al. The SNMMI Practice Guideline for therapy of thyroid disease with 131I3.0. J Nucl Med. 2012;53(10):1633-1651. doi:10.2967/jnumed.112.105148.
    7. Avram AM, Fig LM, Frey KA, Gross MD, Wong KK. Preablation 131-I scans with SPECT/CT in postoperative thyroid cancer patients: what is the impact on staging? J Clin Endocrinol Metab. February 21, 2013 [Epub ahead of print].

    ONC-7: Small Cell Lung Cancer

    ONC-7.0: Small Cell Lung Cancer – General Considerations
    ONC-7.1: Small Cell Lung Cancer – Suspected/Diagnosis
    ONC-7.2: Small Cell Lung Cancer – Initial Work-up/Staging
    ONC-7.3: Small Cell Lung Cancer – Restaging/Recurrence
    ONC-7.4: Small Cell Lung Cancer – Surveillance/Follow-up
    ONC-7.0: Small Cell Lung Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Combined histologies of Small and Non-Small cell are considered Small cell lung cancer. Use this guideline for imaging recommendations for small and large cell high-grade (poorly differentiated) neuroendocrine tumors of the lung.

    Imaging is presently guided by traditional staging of limited or extensive disease.

      ® Extensive stage is either metastatic disease or an extent which cannot be encompassed by a single radiotherapy portal.
      ® Limited staging is confined to one side of the chest.

    Members treated curatively for SCLC are at increased risk for developing a second lung cancer. If new lung nodule is seen on imaging without any evidence of other systemic disease, follow ONC-31.1: Lung Metastases for work-up of nodule.

    For carcinoid (low grade neuroendocrine tumors) of the lung, see: ONC-15: Neuroendocrine Cancers and Adrenal Tumors

    ONC-7.1: Small Cell Lung Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ® Abnormal chest x-ray or clinical suspicion remains high despite a normal chest x-ray in symptomatic member ® CT Chest without contrast (CPT® 71250)
    or
    ® CT Chest with contrast (CPT® 71260)
    ® Pulmonary nodule < 8 mm in size noted on CT Chest® See: CH-16.2: Incidental Pulmonary Nodules Detected on CT Images
    ® Pulmonary nodule 8 mm (0.8 cm) to 30 mm (3 cm) seen on CT Chest or MRI Chest ® See CH-16.4: PET
    ® If PET is Positive: Qualifies as initial staging PET/CT
    Mediastinal/Hilar MassSee also: CH-2: Lymphadenopathy
    Paraneoplastic syndrome suspectedSee also: ONC-30.3: Paraneoplastic Syndromes

    ONC-7.2: Small Cell Lung Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Initial stagingAny or all of the following:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® MRI Brain without and with contrast (CPT® 70553)
    ® Bone scan, if PET/CT not being done (See also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    Confirm limited stage (non-metastatic) disease if initial staging imaging (CT and MRI) shows disease limited to the thorax® PET/CT (CPT® 78815)

    ONC-7.3: Small Cell Lung Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Treatment Response:
    ® After every 2 cycles of chemotherapy
    ® Following completion of chemoradiation
    Any or all of the following:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen with contrast (CPT® 74160)
      ¡ CT Abdomen/Pelvis with contrast (CPT® 74177) may be substituted for known pelvic disease or pelvic symptoms
    ® MRI Brain without and with contrast (CPT® 70553) for measurable brain metastases being treated with systemic therapy
    ® Bone scan (See also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    ® PET is not indicated for evaluation of treatment response in SCLC, but can be considered on a case-by-case basis. These cases should be forwarded for medical director review.
    Restaging (suspected recurrence)Any or all of the following:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen with contrast (CPT® 74160)
      ¡ CT Abdomen/Pelvis with contrast (CPT® 74177) may be substituted for known pelvic disease or pelvic symptoms
    ® Brain MRI without and with contrast (CPT® 70553)
    ® Bone scan (See: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    ® PET is not indicated for evaluation of recurrent SCLC, but can be considered on a case-by-case basis. These cases should be forwarded for Medical Director review.
    Complete or partial response to initial treatment, if prophylactic cranial irradiation (PCI) is planned.® MRI Brain without and with contrast (CPT® 70553)
    ONC-7.4: Small Cell Lung Cancer – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Limited stage SCLC® Every 3 months for one year, every 6 months for two years, and then annually:CT Chest without (CPT® 71250) or CT Chest with contrast (CPT® 71260)
    ® CT Abdomen without (CPT® 74150) or CT Abdomen with contrast (CPT® 74160)
    ® For new nodules, see: ONC-31.1: Lung Metastases
    Extensive stage SCLCEvery 2 months for one year, every 4 months for two years, every 6 months for two years, and then annually:
    ® CT Chest without (CPT® 71250) or CT Chest with contrast (CPT® 71260)
    ® CT Abdomen without (CPT® 74150) or CT Abdomen with contrast (CPT® 74160)
    ® For new nodules, see: ONC-31.1: Lung Metastases
    Screening for brain metastases, regardless of PCI statusMRI Brain without and with contrast (CPT® 70553) every 4 months for one year and then every 6 months for one year


    References

    1. Kalemkerian GP, Loo BW, Akerley W, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2019 – April 9, 2019 Small cell lung cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/sclc.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Small cell Lung cancer V 1.2019 – April 9, 2019 Small ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Lu YY, Chen JH, Liang JA, Chu S, Lin WY, Kao CH. 18F-FDG PET or PET/CT for detecting extensive disease in small-cell lung cancer: a systematic review and meta-analysis. Nucl Med Commun. 2014;35(7):697-703. doi:10.1097/MNM.0000000000000122.
    3. Carter BW, Glisson BS, Truong MT, Erasmus JJ. Small cell lung carcinoma: staging, imaging, and treatment considerations. Radiographics. 2014;34(6):1707-1721. doi:10.1148/rg.346140178.
    4. Kalemkerian G. Staging and imaging of small cell lung cancer. Cancer Imag. 2011;11(1):253-258.

      doi:10.1102/1470-7330.2011.0036.

    ONC-8: Non-Small Cell Lung Cancer
    ONC-8.0: Non-Small Cell Lung Cancer – General Considerations
    ONC-8.1: Non-Small Cell Lung Cancer – Asymptomatic Screening
    ONC-8.2: Non-Small Cell Lung Cancer – Suspected/Diagnosis
    ONC-8.3: Non-Small Cell Lung Cancer – Initial Work-up/Staging
    ONC-8.4: Non-Small Cell Lung Cancer – Restaging/Recurrence
    ONC-8.5: Non-Small Cell Lung Cancer – Surveillance/Follow-up

    ONC-8.0: Non-Small Cell Lung Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Non-small cell lung cancer includes adenocarcinoma, squamous cell carcinoma, adenosquamous and large cell tumors.

    See ONC-15.6: Bronchopulmonary or Thymic Carcinoid – Initial Staging for evaluation of low-grade neuroendocrine tumors (carcinoid) of the lung.

    See ONC-7: Small Cell Lung Cancer for evaluation of high-grade small cell and large cell neuroendocrine tumors of the lung.

    PET/CT scan is not generally indicated for initial staging or restaging of NSCLC with distant metastatic disease, pleural/pericardial effusion, or for multiple sites that are located outside the chest cavity, when found on conventional imaging (i.e., liver, bone and adrenal metastases, etc.).

    PET/CT may be considered to confirm solitary focus of metastatic disease (i.e., brain or adrenal) if being considered for an aggressive surgical management.

    ONC-8.1: Non-Small Cell Lung Cancer – Asymptomatic Screening

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Chest Imaging Policy (Policy #150 in the Radiology Section); CH-34: Lung Cancer Screening for criteria for low-dose CT scan chest for lung cancer screening.

    ONC-8.2: Non-Small Cell Lung Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ® Abnormal chest x-ray or clinical suspicion remains high despite a normal chest x-ray in symptomatic member ® CT Chest without contrast (CPT® 71250)
      or
    ® CT Chest with contrast (CPT® 71260)
    ® Pulmonary nodule < 8 mm in size noted on CT Chest® See: Adult Chest Imaging Policy (Policy #150 in the Radiology Section); CH-16.2: Incidental Pulmonary Nodules Detected on CT Images
    ® Pulmonary nodule 8 mm (0.8 cm) to 30 mm (3 cm) seen on CT Chest or MRI Chest ® See Adult Chest Imaging Policy (Policy #150 in the Radiology Section); CH-16.4: PET
    ® If PET is Positive: Qualifies as initial staging PET/CT
    ® Pulmonary mass 31 mm (3.1 cm) or greater seen on CT or MRI® PET/CT (CPT® 78815) can be approved prior to biopsy if one or more of the following applies:
      ¡ Resection will be performed instead of biopsy if PET confirms limited disease
      ¡ Multiple possible biopsy options are present within the chest and PET findings will be used to determine the most favorable biopsy site
    ® Biopsy is indicated prior to PET imaging for all other indications in pulmonary masses ≥ 31 mm (3.1 cm) in size
    Mediastinal/Hilar MassSee also: Adult Chest Imaging Policy (Policy #150 in the Radiology Section); CH-2: Lymphadenopathy
    Paraneoplastic syndrome suspectedSee also: ONC-30.3: Paraneoplastic Syndromes
    ONC-8.3: Non-Small Cell Lung Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All membersAny or all of the following:
    ® CT Chest (CPT® 71260) with contrast
    ® CT Abdomen (CPT® 74160) with contrast
      ¡ CT Abdomen may be omitted if CT Chest report clearly documents upper abdomen through level of adrenals
    ® Bone scan, if PET/CT not being done
      See also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology
    Any of the following:
    ® All Stage I-IIIB disease
    ® Stage IV disease confined to the chest region
    ® Conventional imaging is inconclusive

    ***PET is not indicated for metastatic disease present outside the chest cavity on CT, MRI, or bone scan

    ® PET/CT (CPT® 78815) if not already completed prior to histological diagnosis
    Any of the following:
    ® All Stage II-IV disease
    ® Stage I disease and considering surgical resection as primary therapy
    ® MRI Brain without and with contrast (CPT® 70553)
    Superior sulcus (Pancoast) tumor suspectedAny or all of the following:
    ® MRI Chest without and with contrast (CPT® 71552)
    ® MRI Cervical spine without and with contrast (CPT® 72156)
    ® MRI Thoracic spine without and with contrast (CPT® 72157)
    ONC-8.4: Non-Small Cell Lung Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Stage I or II members who undergo definitive local treatment with surgery, radiation, or radiosurgery® Restaging imaging is not indicated. See also: Surveillance ONC-8.5: Surveillance/Follow-up
    Measurable disease, undergoing active treatmentAny or all of the following every 2 cycles:
    ® CT Chest with (CPT® 71260) or CT Chest without contrast (CPT® 71250)
    ® CT Abdomen with contrast (CPT® 74160)
      ¡ CT Abdomen/Pelvis with contrast (CPT® 74177) may be substituted for known pelvic disease or pelvic symptoms
    ® MRI Brain without and with contrast (CPT® 70553) for measurable brain metastases being treated with systemic therapy
    Any of the following:
    ® Locally advanced (Stage III, non-metastatic, unresectable)
    ® Inoperable tumor if chemotherapy or chemoradiation was the initial treatment modality
    ® Inadequately resected disease
    ® Suspected recurrence
    Any or all of the following:
    ® CT Chest with (CPT® 71260) or CT Chest without contrast (CPT® 71250)
    ® CT Abdomen with contrast (CPT® 74160)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) may be substituted for known pelvic disease or pelvic symptoms
    Determine resectability following neo-adjuvant therapy® MRI Chest without and with contrast (CPT® 71552)
    Newly identified lung nodule(s)® See ONC-31.1: Lung Metastases for new nodule evaluation
    Any of the following:
    ® Suspected/biopsy proven recurrence localized to the chest cavity
    ® Inconclusive findings conventional imaging
    ® To differentiate tumor from radiation scar/fibrosis
    ® PET/CT (CPT® 78815)

    ***PET is not indicated for metastatic disease present outside the chest cavity on CT, MRI, or bone scan

    Any of the following:
    ® Following a demonstrated adequate response to neoadjuvant therapy if intracranial disease will preclude surgery
    ® Documented recurrence/progression
    ® New or worsening neurological signs or symptoms
    ® MRI Brain without and with contrast (CPT® 70553)
    ONC-8.5: Non-Small Cell Lung Cancer – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Study
    Stage I-II
      CT Chest with contrast (CPT® 71260) or CT Chest without contrast (CPT® 71250) every 6 months for 2 years and then annually

    ***Members treated with radiation therapy and residual abnormality on imaging may undergo CT Chest every 3 months for the first year after therapy, every 6 months in year 2, annually thereafter
    Stage III-IV (metastatic sites treated with definitive intent)® CT Chest with contrast (CPT® 71260) or CT Chest without contrast (CPT® 71250) every 3 months for 2 years, every 6 months for 3 years and then annually
    New lung noduleSee: ONC-31.1: Lung Metastases

    References

    1. Ettinger DS, Wood DE, Aisner DL, et al, National Comprehensive Cancer Network (NCCN) Guidelines Version 5.2019 – June 7, 2019. Non small cell lung cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/nscl.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Non small cell lung cancer V5.2019 – June 7, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. MacMahon H, Naidich DP, Goo JM, et al. Guidelines for management of incidental pulmonary nodules detected on CT images: from the Fleischner Society 2017. Radiology. 2017;284(1):228-243. doi:10.1148/radiol.2017161659.
    3. Calman L, Beaver K, Hind D, Lorigan P, Roberts C, Lloyd-Jones M. Survival benefits from follow-up of patients with lung cancer: a systematic review and meta-analysis. J Thorac Oncol. 2011;6(12):1993-2004. doi:10.1097/JTO.0b013e31822b01a1.
    4. Lou F, Huang J, Sima CS et al. Patterns of recurrence and second primary lung cancer in early-stage lung cancer survivors followed with routine computed tomography surveillance. J Thorac Cardiovasc Surg. 2013;145:75-81. https://www.ncbi.nlm.nih.gov/pubmed/23127371 .
    5. Colt HG, Murgu SD, Korst RJ, et al. Follow-up and surveillance of the patient with lung cancer after curative-intent therapy: diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines, Chest 2013;143:e437S-454S. https://www.ncbi.nlm.nih.gov/pubmed/23649451 .
    6. Dane B, Grechushkin V, Plank A, et al. PET/CT vs. non-contrast CT alone for surveillance 1-year post lobectomy for stage I non-small cell lung cancer. Am J Nucl Med Mol Imaging. 2013; 3:408-416. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784804/ .
    7. Zhao L, He ZY, Zhong XN, et al. (18)FDG-PET/CT for detection of mediastinal nodal metastasis in non-small cell lung cancer: a meta-analysis. Surg Oncol. 2012;21(3):230-236. https://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0049561/ .
    8. Li J, Xu W, Kong F, et al. Meta-analysis: accuracy of 18FDG PET-CT for distant metastasis in lung cancer patients. Surg Oncol. 2013;22(3):151-155. https://www.ncbi.nlm.nih.gov/pubmed/23664848 .
    9. Ravenel JG. Evidence-based imaging in lung cancer: a systematic review. J Thorac Imaging. 2012; 27(5):315-324. http://journals.lww.com/thoracicimaging/Abstract/2012/09000/Evidence_based_Imaging_in_Lung_Cancer__A.8.aspx .
    10. Bille A, Pelosi E, Skanjeti A, et al. Preoperative intrathoracic lymph node staging in patients with non-small-cell lung cancer: accuracy of integrated positron emission tomography and computed tomography. Eur J Cardiothorac Surg. 2009;36(3):440-445. https://academic.oup.com/ejcts/article-lookup/doi/10.1016/j.ejcts.2009.04.003 .


    ONC-9: Esophageal Cancer

    ONC-9.0: Esophageal Cancer – General Considerations
    ONC-9.1: Esophageal Cancer – Suspected/Diagnosis
    ONC-9.2: Esophageal Cancer – Initial Work-up/Staging
    ONC-9.3: Esophageal Cancer – Restaging/Recurrence
    ONC-9.4: Esophageal Cancer – Surveillance/Follow-up

    ONC-9.0: Esophageal Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Clinicians must describe esophageal cancer by cell type and in which third of the esophagus it occurs.

    Cancers of the upper and middle third are usually squamous cell and are highly associated with tobacco and alcohol abuse.

    Cancers of the gastroesophageal (GE) junction are treated as lower third cancers. Lower third cancers are usually adenocarcinomas; 62% of these arise in the setting of Barrett’s esophagus, a condition associated with high body mass index (BMI).

    ONC-9.1: Esophageal Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See also: Adult Neck Imaging Policy (Policy #153 in the Radiology Section); NECK-3.1: Dysphagia for imaging guidelines for evaluation of suspected esophageal malignancy

    ONC-9.2: Esophageal Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Biopsy proven® CT Chest (CPT® 71260) and CT Abdomen with contrast (CPT® 74160)
      ¡ CT Abdomen/Pelvis with contrast (CPT® 74177) may be approved instead of CT Abdomen if there are pelvic signs or symptoms
    Upper 1/3 or neck mass® CT Neck with contrast (CPT® 70491) for upper 1/3 primary and/or neck mass
    If no evidence of metastatic disease by conventional imaging® PET/CT (CPT® 78815)
    ONC-9.3: Esophageal Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    After primary chemoradiation therapy prior to surgery ® CT Chest (CPT® 71260) and CT Abdomen (CPT® 74160) with contrast
    Post-surgical resection® See Surveillance ONC-9.4: Surveillance/Follow-up
    ® If conventional imaging is inconclusive or
    ® Salvage surgical candidate with recurrence and no metastatic disease documented by conventional imaging
    ® PET/CT (CPT® 78815)
      ¡ PET imaging can be done as early as 6 weeks after completion of XRT if recent CT findings are inconclusive and PET findings will alter immediate care decision making
    For any of the following:
    ® Signs or symptoms of recurrence
    ® Biopsy proven on follow-up endoscopy
    ® Recurrence suggested by other imaging (i.e. CXR or barium swallow)
    ® CT Chest (CPT® 71260) and CT Abdomen (CPT® 74160) with contrast
    If previously involved or new signs or symptoms® CT Pelvis with contrast (CPT® 72193) and/or CT Neck with contrast (CPT® 70491)
    ONC-9.4: Esophageal Cancer – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Stage 0-I disease® No routine advanced imaging indicated
    Stage II-III disease® CT Chest (CPT® 71260) and CT Abdomen (CPT® 74160) with contrast every 6 months for 2 years
    Stage IV disease® See: ONC-1.2: Phases of Oncology Imaging and General Phase-Related Considerations

    References

    1. Ajani JA, D’Amico TA, Almhanna K, et al, National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – May 29, 2019. Esophageal and esophagogastric junction cancers, available at: https://www.nccn.org/professionals/physician_gls/pdf/esophageal.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Esophageal and esophagogastric junction cancers V2.2019 – May 29, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Klaeser B, Nitzsche E, Schuller JC, et al. Limited predictive value of FDG-PET for response assessment in the preoperative treatment of esophageal cancer: results of a prospective multi-center trial (SAKK 75/02). Onkologie. 2009;32(12):724-730. doi:10.1159/000251842.
    3. Malik V, Lucey JA, Duffy GJ, et al. Early repeated 18F-FDG PET scans during neoadjuvant chemoradiation fail to predict histopathologic response or survival benefit in adenocarcinoma of the esophagus. J Nucl Med. 2010;51(12):1863-1869. doi:10.2967/jnumed.110.079566.
    4. Stiekema J, Vermeulen D, Vegt E, et al. Detecting interval metastases and response assessment using 18F-FDG PET/CT after neoadjuvant chemoradiotherapy for esophageal cancer. Clin Nucl Med. 2014;39(10):862-867. doi:10.1097/RLU.0000000000000517.
    5. Sudo K, Xiao L, Wadhwa R, et al. Importance of surveillance and success of salvage strategies after definitive chemoradiation in patients with esophageal cancer. J Clin Oncol. 2014;32(30):3400-3405. doi:10.1200/JCO.2014.56.7156.
    6. Lou F, Sima CS, Adusumilli PS, et al. Esophageal cancer recurrence patterns and implications for surveillance. J Thorac Oncol. 2013;8(12):1558–1562. doi:10.1097/01.JTO.0000437420.38972.fb.
    7. Goense L, van Rossum PS, Reitsma JB, et al. Diagnostic performance of 18F-FDG PET and PET/CT for the detection of recurrent esophageal cancer after treatment with curative intent: a systematic review and meta-analysis. J Nucl Med. 2015;56(7):995-1002. doi:10.2967/jnumed.115.155580.


    ONC-10: Other Thoracic Tumors

    ONC-10.1: Malignant Pleural Mesothelioma – Suspected/Diagnosis
    ONC-10.2: Malignant Pleural Mesothelioma – Initial Work-up/Staging
    ONC-10.3: Malignant Pleural Mesothelioma – Restaging
    ONC-10.4: Malignant Pleural Mesothelioma – Surveillance
    ONC-10.5: Thymoma and Thymic Carcinoma – Suspected/Diagnosis
    ONC-10.6: Thymoma and Thymic Carcinoma – Initial Work-up/Staging
    ONC-10.7: Thymoma and Thymic Carcinoma – Restaging
    ONC-10.8: Thymoma and Thymic Carcinoma – Surveillance
    ONC-10.1: Malignant Pleural Mesothelioma – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Chest Imaging Policy (Policy #150 in the Radiology Section); CH-9: Asbestos Exposure for imaging guidelines for evaluation of suspected mesothelioma

    ONC-10.2: Malignant Pleural Mesothelioma – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Cytologically or pathologically proven® CT Chest (CPT® 71260) and CT Abdomen (CPT® 74160) with contrast
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) may be approved instead of CT Abdomen if there are pelvic signs or symptoms
    ® PET/CT (CPT® 78815) if no evidence of metastatic disease or inconclusive conventional imaging
    Preoperative planning® MRI Chest without and with contrast (CPT® 71552)
    ONC-10.3: Malignant Pleural Mesothelioma – Restaging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Signs or symptoms of recurrence® CT Chest (CPT® 71260) and CT Abdomen (CPT® 74160) with contrast
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) may be approved instead of CT Abdomen if there are pelvic signs or symptoms
    Treatment with chemotherapyEvery 2 cycles:
    ® CT Chest (CPT® 71260) and CT Abdomen (CPT® 74160) with contrast
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) may be approved instead of CT Abdomen if there are pelvic signs or symptoms
    Following induction chemotherapy prior to surgical resection® CT Chest (CPT® 71260) and CT Abdomen (CPT® 74160) with contrast
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) may be approved instead of CT Abdomen if there are pelvic signs or symptoms
    ® PET/CT (CPT® 78815) if no evidence of metastatic disease
    Inconclusive Chest CT® MRI Chest without and with contrast (CPT® 71552)
    ONC-10.4: Malignant Pleural Mesothelioma – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All® CT Chest with contrast (CPT® 71260) and previously involved regions every 3 months for 2 years, then annually thereafter
    ONC-10.5: Thymoma and Thymic Carcinoma – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Chest Imaging Policy (Policy #150 in the Radiology Section); CH-20: Mediastinal Mass for imaging guidelines for evaluation of suspected thymic malignancies

    See ONC-15.6:Bronchopulmonary or Thymic Carcinoid – Initial Staging for imaging guidelines for thymic carcinoid

    ONC-10.6: Thymoma and Thymic Carcinoma – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Encapsulated or invasive limited disease® CT Chest with contrast (CPT® 71260)
    Extensive mediastinal involvement on Chest CT® CT Abdomen with contrast (CPT® 74160)
    ® CT Neck with contrast (CPT® 70491)
    Inconclusive finding on CTOne of the following:
    ® PET/CT (CPT® 78815)
    ® MRI Chest without and with contrast (CPT® 71552)
    Preoperative planning® MRI Chest without and with contrast (CPT® 71552)
    Thymic Carcinomas® Image according to ONC-8: Non-Small Cell Lung Cancer
    ONC-10.7: Thymoma and Thymic Carcinoma – Restaging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Study
    Adjuvant therapy following surgical resection® Follow surveillance imaging
    For suspected recurrence® CT Chest with contrast (CPT® 71260)
    Recurrence with extensive mediastinal involvement on chest CT® CT Abdomen with contrast (CPT® 74160)
    ® CT Neck with contrast (CPT® 70491)
    Thymic carcinomasSee ONC-8: Non-Small Cell Lung Cancer
    Inconclusive finding on CTOne of the following:
    ® PET/CT (CPT® 78815)
    ® MRI Chest without and with contrast (CPT® 71552)
    Extensive disease on chemotherapy® CT Neck (CPT® 70491), CT Chest (CPT® 71260), and CT Abdomen (CPT® 74160) with contrast, every 2 cycles of therapy
    ® Following induction chemotherapy prior to surgical resection, PET/CT (CPT® 78815) if no evidence of metastatic disease
    ONC-10.8: Thymoma and Thymic Carcinoma – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Study
    Thymoma ® CT Chest with contrast (CPT® 71260) and previously involved regions every 6 months for 2 years, then annually for next 10 years
    Thymic carcinomas® CT Chest with contrast (CPT® 71260) every 6 months for 2 years and then annually for 5 years
    References

    1. Ettinger DS, Wood DE , Aisner DL et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – April 1, 2019. Malignant Pleural Mesothelioma, available at: https://www.nccn.org/professionals/physician_gls/pdf/mpm.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Malignant Pleural Mesothelioma V2.2019 – April 1, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Ettinger DS, Wood DE , Aisner DL et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – March 11, 2019. Thymoma and Thymic carcinoma, available at: https://www.nccn.org/professionals/physician_gls/pdf/thymic.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Thymoma and Thymic carcinoma, V 2.2019 – March 11, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    3. Sørensen JB, Ravn J, Loft A, Brenøe J, Berthelsen AK, Nordic Mesothelioma Group. Preoperative staging of mesothelioma by 18F-fluoro-2-deoxy-D-glucose positron emission tomography/computer tomography fused imaging and mediastinoscopy compared to pathological findings after extrapleural pneumonectomy. Eur J Cardiothorac Surg. 2008;34:1090-1096. doi:10.1016/j.ejcts.2008.07.050.
    4. Wilcox BE, Subramaniam RM, Peller PJ, et al. Utility of computed tomography-positron emission tomography for selection of operable malignant pleural mesothelioma. Clin lung cancer. 2009;10:244-248. doi: 10.3816/CLC.2009.n.033.
    5. Marom EM. Imaging thymoma. J Thorac Oncol. 2010;5(10 Suppl 4):S296-S303. doi:10.1097/JTO.0b013e3181f209ca.
    6. Marom EM. Advances in thymoma imaging. J Thorac Imaging. 2013;28(2):69-80. doi:10.1097/RTI.0b013e31828609a0.
    7. Hayes SA, Huang J, Plodkowski AJ, et al. Preoperative computed tomography findings predict surgical resectability of thymoma. J Thorac Oncol. 2014;9(7):1023-1030. doi:10.1097/JTO.0000000000000204.
    8. Mineo TC, Ambrogi V. Malignant pleural mesothelioma: factors influencing the prognosis. Oncology. 2012;26(12):1164-75.

    ONC-11: Breast Cancer

    ONC-11.0: Breast Cancer – General Considerations
    ONC-11.1: Breast Cancer – Suspected/Diagnosis
    ONC-11.2: Breast Cancer – Initial Work-up/Staging
    ONC-11.3: Breast Cancer – Restaging/Recurrence
    ONC-11.4: Breast Cancer – Surveillance/Follow-up
    ONC-11.0: Breast Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Advanced imaging to evaluate for distant metastases is not indicated for pre-invasive or in-situ breast cancer (histologies such as DCIS and LCIS). Bone scan has a high concordance rate with PET for detecting bone metastases.

    Scintimammography and Breast Specific Gamma Imaging (BSGI) are considered investigational.

    NOTE: Some payors have specific restrictions on PET imaging, and those coverage policies may supersede the recommendations for PET imaging in these guidelines.

    PET is not indicated for the following:

      ® Non-invasive breast cancers
      ® Prior to lymph node sampling in a member with clinical stage I, II, or operable IIIA disease
      ® Obvious multi-organ metastatic disease is present on CT or MRI


    ONC-11.1: Breast Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Breast Imaging Policy (Policy #177 in the Radiology Section); BR-5: Breast MRI Indications for imaging guidelines for evaluation of suspected breast cancer

    ONC-11.2: Breast Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Any of the following:
    ® Biopsy proven invasive breast cancer or carcinoma in-situ
    ® Adenocarcinoma in axillary lymph node
    ® Bilateral Breast MRI (CPT® 77049)
    Operable disease (stage I and II)® No advanced imaging needed
    ® For planned sentinel lymph node (SLN) biopsy: Lymph system imaging (lymphoscintigraphy, CPT® 78195)
    Clinical Stage III and Stage IV disease or for signs or symptoms of systemic disease (including elevated liver function tests or tumor markers)Any or all of the following:
    ® CT Chest with contrast (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® Bone scan
    See also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology
    Inconclusive CT and bone scan ® PET/CT (CPT® 78815)
    Bone pain® Bone scan (see: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    ® See also: ONC-31.5: Bone (including Vertebral) Metastases
    ® See also: ONC-31.6: Spinal Cord Compression
    ONC-11.3: Breast Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Any of the following:
    ® Biopsy proven local recurrence
    ® Suspicion of recurrence with inconclusive mammogram and/or ultrasound (BIRADS 0)
    ® Mammogram and ultrasound conflicts with physical exam
    ® End of planned neoadjuvant chemotherapy to determine resectability
      Bilateral MRI Breast without and with contrast (CPT® 77049)
    Any of the following:
    ® Elevated LFTs
    ® Rising tumor markers
    ® Signs or symptoms of recurrence
    ® Biopsy proven recurrence
      Any or all of the following:
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® Bone scan (See also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    Treatment response in members with metastatic disease and measurable disease on imaging
      Any or all of the following for members being treated with chemotherapy, every 2 cycles:
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® Bone scan (see also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    ® MRI Brain without and with contrast (CPT® 70553) for members receiving systemic treatment for brain metastases
      Any or all of the following for members being treated with endocrine/hormonal therapy, every 3 months:
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® Bone scan (See ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    Inconclusive CT, MRI, and/or bone scan for suspected recurrence, and further characterization is needed to make treatment decisions® PET/CT (CPT® 78815)
    Any of the following:
    ® Assessing for residual disease after surgery
    ® Assessing response to neoadjuvant chemotherapy
    ® After lumpectomy or mastectomy, prior to adjuvant therapy
    ® Neither PET nor CT are indicated for systemic restaging after neoadjuvant chemotherapy or after surgery
    Bone metastasis as the only site of stage IV disease (excluding brain metastases) and a prior bone scan has not been performed for serial comparison® PET/CT (CPT® 78815)
    ONC-11.4: Breast Cancer – Surveillance/Follow–up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Metastatic disease on a break from therapy with persistent measurable diseaseAny or all of the following, every 3 months:
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® Bone scan (see also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    Asymptomatic non-metastatic disease® No advanced imaging indicated
    Breast imaging surveillance, including after bilateral mastectomy® See BR-5: Breast MRI Indications for imaging guidelines
    References

    1. Gradishar WJ, Anderson BO, Balassanian R et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – July 2, 2019. Breast cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/breast.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Breast Cancer V 2.2019 – July 2, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Cardoso F, Costa A, Norton L, et al. ESO-ESMO 2nd international consensus guidelines for advanced breast cancer (ABC2). Ann Oncol. 2014;25(10):1871-1888. doi:10.1093/annonc/mdu385.
    3. Khatcheressian JL, Hurley P, Bantug E, et al. Breast cancer follow-up and management after primary treatment: American Society of Clinical Oncology clinical practice guideline update. J Clin Oncol. 2013;31:961-965. doi:10.1200/JCO.2012.45.9859.
    4. Puglisi F, Follador A, Minisini AM, et al. Baseline staging tests after a new diagnosis of breast cancer: further evidence of their limited indications. Ann Oncol. 2005;16(2):263-266. doi:10.1093/annonc/mdi063.
    5. Rong J, Wang S, Ding Q, Yun M, Zheng Z, Ye S. Comparison of 18 FDG PET-CT and bone scintigraphy for detection of bone metastases in breast cancer patients. A meta-analysis. Surg Oncol. 2013;22(2):86-91. doi:10.1016/j.suronc.2013.01.002.
    6. Hong S, Li J, Wang S. 18FDG PET-CT for diagnosis of distant metastases in breast cancer patients. A meta-analysis. Surg Oncol. 2013;22(2):139-143. doi:10.1016/j.suronc.2013.03.001.
    7. Cheng X, Li Y, Liu B, Xu Z, Bao L, Wang J. 18F-FDG PET/CT and PET for evaluation of pathological response to neoadjuvant chemotherapy in breast cancer: a meta-analysis. Acta Radiol. 2012;53(6):615-627. doi:10.1258/ar.2012.110603.
    8. Simos D, Catley C, van Walraven C, et al. Imaging for distant metastases in women with early-stage breast cancer: a population-based cohort study. CMAJ. 2015;187(12):E387-E397. doi:10.1503/cmaj.150003.
    9. Crivello ML, Ruth K, Sigurdson ER, et al. Advanced imaging modalities in early stage breast cancer: preoperative use in the United States Medicare population. Ann Surg Oncol. 2013;20(1):102-110. doi:10.1245/s10434-012-2571-4.

    ONC-12: Sarcomas – Bone, Soft Tissue and GIST
    ONC-12.1: Bone and Soft Tissue Sarcomas – General Considerations
    ONC-12.2: Soft Tissue Sarcomas – Initial Work-up/Staging
    ONC-12.3: Soft Tissue Sarcomas – Restaging/Recurrence
    ONC-12.4: Soft Tissue Sarcomas – Surveillance/Follow-up
    ONC-12.5: Gastrointestinal Stromal Tumor (GIST)
    ONC-12.6: Bone Sarcomas – Initial Work-up/Staging
    ONC-12.7: Bone Sarcomas – Restaging/Recurrence
    ONC-12.8: Bone Sarcomas – Surveillance/Follow-up
    ONC-12.9: Benign Bone Tumors – General Considerations
    ONC-12.10: Benign Bone Tumors – Initial Work-up/Staging
    ONC-12.11: Benign Bone Tumors – Restaging/Recurrence
    ONC-12.12: Benign Bone Tumors – Surveillance/Follow-up
    ONC-12.1: Bone and Soft Tissue Sarcomas - General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Sarcomas are tumors of mesenchymal origin, classified as high-, intermediate-, and low-grade (G) tumors (sometimes described as “spindle cell” cancers). They can arise in any bony, cartilaginous, smooth muscle, skeletal muscle, or cardiac muscle tissue.

    Sarcomas occur in both adult and pediatric members, but some are more common in one age group than the other. Unless specified below, members age ≥ 18 years old should be imaged according to this guideline section.

    Exceptions include:

    Rhabdomyosarcoma members of all ages should be imaged according to guidelines in Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-8.2: Rhabdomyosarcoma

    Osteogenic sarcoma (Osteosarcoma) members of all ages should be imaged according to guidelines in Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-9.3: Osteogenic Sarcoma (OS)

    Ewing sarcoma and Primitive Neuroectodermal Tumor members of all ages should be imaged according to guidelines in Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-9.4: Ewing Sarcoma and Primitive Neuroectodermal Tumors (ESFT)

    Kaposi’s sarcoma members of all ages should be imaged according to guidelines in ONC-31.10: Kaposi’s Sarcoma


    ONC-12.2: Soft Tissue Sarcomas - Initial Workup/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Retroperitoneal or intraabdominal primary siteAny or all of the following:
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ® Either CT Abdomen/Pelvis with contrast (CPT® 74177) or MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast
    Any of the following:
    ® Extremity or trunk primary site
    ® Head or neck primary site
    ® Other histologies documented to have propensity for lymphatic spread and deep-seated tumors
    Any or all of the following:
    ® MRI without and with contrast of involved area
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    Any of the following:
    ® Angiosarcoma
    ® Alveolar soft part sarcoma
    ® Clear cell sarcoma
    ® Epithelioid sarcoma
    ® Hemangiopericytoma
    ® Leiomyosarcoma
    ® Other histologies documented to have propensity for lymphatic spread and deep-seated tumors
    Any or all of the following:
    ® MRI without and with contrast of involved area
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ® Either CT Abdomen/Pelvis with contrast (CPT® 74177) or MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast
    Myxoid round cell liposarcomaAny or all of the following:
    ® MRI without and with contrast of involved area
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ® Either CT Abdomen/Pelvis with contrast (CPT® 74177) or MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast
    ® MRI Cervical/Thoracic/Lumbar spine without and with contrast (CPT® 72156, CPT® 72157, and CPT® 72158)
    Any of the following:
    ® Angiosarcoma
    ® Alveolar soft part sarcoma
    ® All members with signs/symptoms of brain metastases
    ® MRI Brain without and with contrast (CPT® 70553)
    Any of the following:
    ® Grade of tumor in doubt following biopsy
    ® Conventional imaging suggests solitary metastasis amenable to surgical resection
    ® PET/CT (CPT® 78815 or CPT® 78816)
    Desmoid TumorsOne of the following:
    ® CT without contrast or with contrast of the affected body part
    ® MRI without contrast or without and with contrast of the affected body part
    ® Imaging of lung, lymph node, and metastatic site for these tumors is not indicated
    Dermatofibrosarcoma Protuberans (DFSP)
      One of the following:
      ® CT without contrast or with contrast of the affected body part
      ® MRI without contrast or without and with contrast of the affected body part
      ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250) for
          ¡ pulmonary symptoms
          ¡ abnormal chest x-ray
          ¡ sarcomatous differentiation


    ONC-12.3: Soft Tissue Sarcomas - Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Any of the following:
    ® After preoperative radiotherapy
    ® After surgical resection
    ® After adjuvant radiotherapy
    ® MRI without and with contrast of affected body area
    ® CT without contrast or with contrast can be added if demonstrated bone involvement
    ® Chest or lymph node imaging is not indicated if no abnormality on previous imaging
    Any of the following:
    ® Differentiate tumor from radiation or surgical fibrosis
    ® Determine response to neoadjuvant therapy
    ® Confirm oligometastatic disease prior to curative intent surgical resection
    ® PET/CT (CPT® 78815 or CPT® 78816)
    Chemotherapy response for members with measurable disease® CT with contrast or MRI without and with contrast of affected body area every 2 cycles
    Local recurrence suspected® Repeat all imaging for initial workup of specific histology and/or primary site
    Preoperative planning prior to resection Any or all of the following:
    ® MRI without contrast or without and with contrast of involved area
    ® CT (contrast as requested) of involved area
    Dermatofibrosarcoma Protuberans (DFSP)
      One of the following:
      ® CT without contrast or with contrast of the affected body part
      ® MRI without contrast or without and with contrast of the affected body part
      ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250) for:
        ¡ pulmonary symptoms
        ¡ abnormal chest x-ray
        ¡ sarcomatous differentiation


    ONC-12.4: Soft Tissue Sarcomas Surveillance/Follow Up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Retroperitoneal/intra-abdominal primary site Any or all of the following every 3 months for 2 years, then every 6 months for 2 more years, then annually:
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast or MRI without and with contrast of any other involved body areas
    Extremity, trunk, or Head/Neck primary site, low grade Stage I diseaseAny or all of the following every 6 months for 2 years, then annually until year 10:
    ® Chest x-ray
        ¡ CT Chest with (CPT® 71260) or without contrast (CPT® 71250) is indicated for new findings on CXR or new/worsening pulmonary signs/symptoms
    ® CT with contrast, MRI without contrast, or MRI without and with contrast of primary site if primary site not easily evaluated by physical exam
    Extremity, trunk, or Head/Neck primary site, Stages II-IV disease.Any or all of the following every 3 months for 2 years, then every 6 months for 2 more years, then annually:
    ® CT with contrast, MRI without contrast, or MRI without and with contrast of primary site
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ® CT with contrast or MRI without and with contrast of any other involved body areas
    Desmoid tumorsOne of the following every 6 months for 3 years, then annually:
    ® CT without contrast or with contrast of the affected body part
    ® MRI without contrast or without and with contrast of the affected body part
    Dermatofibrosarcoma Protuberans® No routine imaging unless clinical signs/symptoms of recurrence
    ONC-12.5: Gastrointestinal Stromal Tumor (GIST)

    For this condition imaging is medically necessary based on the following criteria:

    General Considerations
    GISTs are mesenchymal neoplasms of the gastrointestinal (GI) tract, mostly found in the stomach and upper small bowel, commonly metastasizing to the liver and abdominal cavity and primarily treated with surgery.

    Indication
    Imaging Study
    Suspected/Diagnosis® CT Abdomen/Pelvis with contrast (CPT® 74177)
    Initial Work-up/Staging® CT Chest (CPT® 71260 ) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® MRI Abdomen without and with contrast (CPT® 74183) is indicated for evaluation of liver lesions that are equivocal on CT imaging or for preoperative assessment of liver
    ® PET is indicated for evaluation of inconclusive findings on conventional imaging
    Restaging/Recurrence® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Chest with contrast (CPT® 71260) if prior evidence of chest disease or signs or symptoms of chest disease
    ® PET is indicated for evaluation of inconclusive findings on conventional imaging
    Treatment Response® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Chest with contrast (CPT® 71260) if prior evidence of chest disease or signs or symptoms of chest disease
    ® PET is indicated for evaluation of inconclusive findings on conventional imaging
    Surveillance/Follow-up® CT Abdomen/Pelvis with contrast (CPT® 74177) every 6 months for 5 years, then annually


    ONC-12.6: Bone Sarcomas - Initial Workup/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ChondrosarcomaAny or all of the following:
    ® MRI without contrast or without and with contrast of involved area
    ® CT (contrast as requested) of involved area
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ChordomaAny or all of the following:
    ® MRI without contrast or without and with contrast of involved area
    ® CT (contrast as requested) of involved area
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® MRI Cervical (CPT® 72156), Thoracic (CPT® 72157), and Lumbar spine (CPT® 72158) without and with contrast
    ® Bone scan (see also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    ® PET may be approved for inconclusive conventional imaging
    ONC-12.7: Bone Sarcomas - Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ChondrosarcomaAny or all of the following, after completion of radiotherapy or every 2 cycles of chemotherapy:
    ® MRI without contrast or without and with contrast of involved area
    ® CT (contrast as requested) of involved area
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ChordomaAny or all of the following, after completion of radiotherapy or every 2 cycles of chemotherapy:
    ® MRI without contrast or without and with contrast of involved area
    ® CT (contrast as requested) of involved area
    ® Bone scan (see also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    ® PET may be approved for inconclusive conventional imaging


    ONC-12.8: Bone Sarcomas - Surveillance/Follow Up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ® Grade I Chondrosarcoma
    ® Intracompartmental Chondrosarcoma
    Any or all of the following every 6 months for 2 years, then annually for 10 years:
    ® Plain x-ray of primary site
      ¡ MRI without and with contrast is indicated for new findings on plain x-ray or new/worsening clinical symptoms.
    ® Chest x-ray
      ¡ CT Chest with (CPT® 71260) or without contrast (CPT® 71250) for new findings on CXR, or new/worsening signs/symptoms.
    ® Grade II or III Chondrosarcoma
    ® Clear Cell Chondrosarcoma
    ® Extracompartmental Chondrosarcoma
    Any or all of the following every 6 months for 5 years, then annually for 10 years:
    ® Plain x-ray of primary site
      ¡ MRI without and with contrast is indicated for new findings on plain x-ray or new/worsening clinical symptoms.
    ® Chest x-ray or CT Chest with (CPT® 71260) or CT Chest without contrast (CPT® 71250)
    ChordomaAny or all of the following every 6 months for 5 years, then annually until year 10:
    ® Plain x-ray of primary site
      ¡ MRI without and with contrast is indicated for new findings on plain x-ray or new/worsening clinical symptoms.
    ® Chest x-ray
      ¡ CT Chest with (CPT® 71260) or without contrast (CPT® 71250) for new findings on CXR, or new/worsening signs/symptoms
    ONC-12.9: Benign Bone Tumors - General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Variety of diagnoses, including osteoid osteochondroma, chondroblastoma, desmoplastic fibroma, Paget’s disease, osteoid osteoma and others

    Plain x-ray appearance is diagnostic for many benign bone tumors and advanced imaging is generally unnecessary except for preoperative planning

    MRI without and with contrast is the primary modality for advanced imaging of bone tumors, and can be approved to help narrow differential diagnoses and determine whether biopsy is indicated

    Some benign bone tumor types carry a risk of malignant degeneration over time, but routine advanced imaging surveillance has not been shown to improve outcomes for these members

    MRI without and with contrast can be approved to evaluate new findings on plain x-ray new/worsening clinical symptoms not explained by a recent plain x-ray

    There are no data to support the use of PET/CT in the evaluation of benign bone tumors, and PET requests should not be approved without biopsy confirmation of a malignancy
    Other benign bone tumor members of all ages should be imaged according to guidelines in Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-9.2: Benign Bone Tumors


    ONC-12.10: Benign Bone Tumors - Initial Workup/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Giant Cell Tumor of Bone (GCTB)Any or all of the following:
    ® MRI without contrast or without and with contrast of involved area
    ® CT (contrast as requested) of involved area
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ® Bone scan (see also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    Enchondroma® MRI without contrast or without and with contrast of primary site

    ONC-12.11: Benign Bone Tumors - Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Giant Cell Tumor of Bone (GCTB)Any or all of the following, after completion of radiotherapy or every 2 cycles of chemotherapy:
    ® MRI without contrast or without and with contrast of involved area
    ® CT (contrast as requested) of involved area
    ® Bone scan (see also: ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    EnchondromaGenerally no indication for this benign tumor unless symptoms
    ONC-12.12: Benign Bone Tumors - Surveillance/Follow Up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Giant Cell Tumor of Bone (GCTB)
      Any or all of the following every 6 months for 2 years, then annually thereafter:
      ® Plain x-ray of primary site
      ¡ MRI without and with contrast is indicated for new findings on plain x-ray or new/worsening clinical symptoms.
      ® Chest x-ray
      ¡ CT Chest with (CPT® 71260) or without contrast (CPT® 71250) for new findings on CXR, or new/worsening signs/symptoms.
    Enchondroma Plain films of primary site

    References

    1. Mehren MV, Randall RL, Benjamin RS, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – February 4, 2019. Soft Tissue Sarcoma, available at: https://www.nccn.org/professionals/physician_gls/pdf/sarcoma.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Soft Tissue Sarcoma V 2.2019 – February 4, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Biermann JS, Chow W, Adkins DR, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – April 10, 2019. Bone cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/bone.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Bone cancer V 2.2019 – April 10, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    3. Nishiguchi T, Mochizuki K, Ohsawa M, et al, Differentiating benign notochordal cell tumors from chordomas: radiographic features on MRI, CT, and tomography. Am Jour Roentgenol. 2011;196(3):644-650. doi:10.2214/AJR.10.4460.
    4. Van den Abbeele AD. The lessons of GIST-PET and PET/CT: a new paradigm for imaging. Oncologist. 2008;13:8-13. doi:10.1634/theoncologist.13-S2-8.
    5. Demetri GD, von Mehren M, Antonescu CR, et al. NCCN Task Force report: update on the management of patients with gastrointestinal stromal tumors. J Natl Compr Canc Netw. 2010;8(Suppl 2):S42-44.
    6. Peng PD, Hyder O, Mavros MN, et al. Management and recurrence patterns of desmoids tumors: a multi-institutional analysis of 211 patients. Ann Surg Oncol. 2012;19(13):4036-4042. doi:10.1245/s10434-012-2634-6.
    7. Tseng WW, Amini B, Madewell JE. Follow-up of the soft tissue sarcoma patient. J Surg Oncol. 2015;111(5):641-645. doi:10.1002/jso.23814.
    8. Grotz TE, Donohue JH. Surveillance strategies for gastrointestinal stromal tumors. J Surg Oncol. 2011;104(8):921-927. doi:10.1002/jso.21862.
    9. Akram J, Wooler G, Lock-Andersen J. Dermatofibrosarcoma protuberans: clinical series, national Danish incidence data and suggested guidelines. J Plast Surg Hand Surg. 2014;48(1):67-73. doi:10.3109/2000656X.2013.812969.
    10. Puri A, Gulia A, Hawaldar R, Ranganathan P, Badwe RA. Does intensity of surveillance affect survival after surgery for sarcomas? Results of a randomized noninferiority trial. Clin Orthop Relat Res. 2014;472(5):1568-1575. doi:10.1007/s11999-013-3385-9.
    11. Biermann JS, Adkins DR, Aqulnik M, et al. Bone cancer. J Natl Compr Canc Netw. 2013;11(6):688-723.

    ONC-13: Pancreatic Cancer
    ONC-13.0: Pancreatic Cancer – General Considerations
    ONC-13.1: Pancreatic Cancer – Screening Studies for Pancreatic Cancer
    ONC-13.2: Pancreatic Cancer – Suspected/Diagnosis
    ONC-13.3: Pancreatic Cancer – Initial Work-up/Staging
    ONC-13.4: Pancreatic Cancer – Restaging/Recurrence
    ONC-13.5: Pancreatic Cancer – Surveillance/Follow-up


    ONC-13.0: General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    This guideline refers only to adenocarcinoma of the exocrine pancreas, which accounts for over 90% of pancreatic malignancies. This guideline may also be used for cancer of the Ampulla of Vater.

    Neuroendocrine and carcinoid tumors of the pancreas are not included in this guideline, see: ONC-15: Neuroendocrine Cancers and Adrenal Tumors

    ONC-13.1: Pancreatic Cancer – Screening Studies for Pancreatic Cancer

    For this condition imaging is medically necessary based on the following criteria:

    Detailed history of any known inherited syndrome in the member and detailed family history in first and second degree relatives, including the age and lineage, is essential to guide screening recommendations. See table below for age- and risk-specific screening recommendations

    New onset of diabetes in members older than 50 has been recognized as a potential indicator of the development of pancreatic cancer. Approximately 1% of members in this category are diagnosed with cancer within 3 years. A prediction model has been established which identifies those members at greatest risk for pancreatic malignancy. The scoring system, known as ENDPAC (Enriching New-Onset Diabetes for Pancreatic Cancer) is based on 3 discriminatory factors, including change in blood glucose, change in weight, and age of onset at the time of the new diagnosis of diabetes. A score of > 3 imparts an elevated risk of pancreatic cancer (3.6%), and these members should be screened. Screening is not indicated at this time for scores of 0-2.

    Indications
    Imaging Study
    Age 50 or 10 years earlier than the youngest affected family member when BOTH of the following are met:
    ® First- or second-degree relative affected with pancreatic cancer AND
    ® Known mutation carrier of one of the following genes:
      ¡ Lynch Syndrome
      ¡ BRCA1, BRCA2 (Familial Breast and Ovarian syndrome)
      ¡ PALB2 mutation
      ¡ ATM (Ataxia-Telangiectasia)
    ® MRI Abdomen without and with contrast (CPT® 74183) at baseline, repeat annually
    Age 50 or 10 years earlier than the youngest affected family member for ANY of the following:
    ® Individuals with 2 relatives with pancreatic adenocarcinoma where one is a first-degree relative
    ® Individuals with 3 or more relatives with pancreatic cancer
    ® Familial Atypical Multiple Melanoma and Mole Syndrome (FAMM-mutations in CDKN2A gene, p16, or multiple tumor suppressor-1 gene)
    ® Hereditary Pancreatitis (PRSS1 Gene)
    ® MRI Abdomen without and with contrast (CPT® 74183) at baseline, repeat annually
    Peutz-Jeghers Syndrome® MRI Abdomen without and with contrast (CPT® 74183) starting at age 30, repeat annually
    Screening MRI reveals cystic lesion of the pancreas® Repeat MRI Abdomen without and with contrast (CPT® 74183) in 6 months
    Screening MRI reveals indeterminate solid lesion ® Repeat MRI Abdomen without and with contrast (CPT® 74183) in 3 months
    Screening MRI reveals pancreatic stricture® Repeat MRI Abdomen without and with contrast (CPT® 74183) in 3 months
    For any of the following:
    ® Familial Adenomatous Polyposis Syndrome (APC gene)
    ® Hereditary pancreatic neuroendocrine tumors (Multiple Endocrine Neoplasia Type I [MEN-1]
    ® Von Hippel-Lindau disease
    ® Neurofibromatosis Type 1
    ® Tuberous sclerosis
    ® Li-Fraumeni syndrome
    ® Advanced imaging is not routinely indicated for screening for pancreatic cancer
    New onset diabetes in adults with ENDPAC score of ≥3® CT Abdomen without and with contrast (CPT® 74170) or MRI Abdomen without and with contrast (CPT® 74183) at baseline; if negative, can be repeated once after 6 months

    ONC-13.2: Pancreatic Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    For any suspected symptoms only® Ultrasound (CPT® 76700 or CPT® 76705)
    Symptoms and abnormal lab(s), or physical exam findings, or abnormal ultrasound/ERCP® CT Abdomen without and with contrast (CPT® 74170) or MRI Abdomen without and with contrast (CPT® 74183)
    Preoperative studies for potentially resectable tumors without confirmed histologic diagnosis® See also: ONC-13.3: Pancreatic Cancer – Initial Work-up/Staging

    ONC-13.3: Pancreatic Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All members® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with (CPT® 74177) or CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® EUS
    Preoperative planning or CT insufficient to determine resectability ® MRI Abdomen without and with contrast (CPT® 74183)
    No evidence of metastatic disease on CT or MRI® PET/CT (CPT® 78815)


    ONC-13.4: Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    For any of the following:
    ® After neoadjuvant chemoradiation
    ® Suspected recurrence
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with (CPT® 74177) or CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® CT with contrast of other involved or symptomatic areas
    ® PET/CT (CPT® 78815) for inconclusive conventional imaging post chemoradiation
    Unresectable disease or metastatic disease on chemotherapyEvery 2 cycles of treatment (commonly every 6 to 8 weeks):
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with (CPT® 74177) or CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® CT with contrast of other involved or symptomatic areas
    Unexplained elevated liver enzymes or inconclusive recent CT abnormality ® MRI Abdomen without and with contrast (CPT® 74183)
    If complete surgical resection was initial therapy® See also: ONC-13.5: Pancreatic Cancer – Surveillance/Follow-up for surveillance imaging


    ONC-13.5: Surveillance/Follow Up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All membersEvery 3 months for 2 years, then annually:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Chest with contrast (CPT® 71260)


    References

    1. Tempero MA, Malafa MP, Al-Hawary M, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 3.2019 – July 2, 2019. Pancreatic adenocarcinoma, available at: https://www.nccn.org/professionals/physician_gls/pdf/pancreatic.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Pancreatic adenocarcinoma V 3.2019 – July 2, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org .
    2. Syngal S, Brand RE, Church JM, et al. ACG clinical guideline: genetic testing and management of hereditary gastrointestinal cancer syndromes. Am. J. Gastroenterol. 2015;110(2):223-262. doi:10.1038/ajg.2014.435.
    3. Canto MI, Harinck F, Hruban RH, et al. International Cancer of the Pancreas Screening (CAPS) consortium summit on the management of patients with increased risk for familial pancreatic cancer. Gut. 2013;62(3):339-347. doi:10.1136/gutjnl-2012-303108.
    4. U.S. Preventive Services Task Force. Screening for pancreatic cancer: recommendation statement. Rockville, Maryland: Agency for Healthcare Research and Quality (AHRQ); 2004.
    5. Heinrich S, Goerres GW, Schafer M, et al. Positron emission tomography/computed tomography influences on the management of resectable pancreatic cancer and its cost-effectiveness. Ann Surg. 2005;242(2):235-243.
    6. Gemmel C, Eickhoff A, Helmstädter L, Riemann JF. Pancreatic cancer screening: state of the art. Expert Rev Gastroenterol Hepatol. 2009;3(1):89-96. doi:10.1586/17474124.3.1.89.
    7. Al-Hawary MM, Francis IR, Chari ST, et al. Pancreatic ductal adenocarcinoma radiology reporting template: consensus statement of the Society of Abdominal Radiology and the American Pancreatic Association. Gastroenterology. 2014;146(1):291-304. doi:10.1053/j.gastro.2013.11.004.
    8. Tersmette AC, Petersen GM, Offerhaus GJ. Increased risk of incident pancreatic cancer among first-degree relatives of patients with familial pancreatic cancer. Clin Cancer Res. 2001;7(3):738-44.
    9. Tzeng CW, Abbott DE, Cantor SB et al. Frequency and intensity of postoperative surveillance after curative treatment of pancreatic cancer: a cost-effectiveness analysis. Ann Surg Oncol. 2013;20(7):2197-2203. doi:10.1245/s10434-013-2889-6.
    10. Furman MJ, Lambert LA, Sullivan ME, Whalen GF. Rational follow-up after curative cancer resection. Journal of Clinical Oncology. 2013;31(9):1130-1133. doi:10.1200/JCO.2012.46.4438.
    11. Tzeng C, Fleming J, Lee J, et al. Yield of clinical and radiographic surveillance in patients with resected pancreatic adenocarcinoma following multimodal therapy. HPB. 2012;14(6):365-372. doi:10.1111/j.1477-2574.2012.00445.x.
    12. Sharma, A, Kandlakunta H, Nagpal SJS, et.al. Model to determine risk of pancreatic cancer in patients with new-onset diabetes. Gastroenterology. 2018;155(3):730-739.


    ONC-14: Upper GI Cancers
    ONC-14.1: Hepatocellular Carcinoma (HCC) – General Considerations
    ONC-14.2: Hepatocellular Carcinoma (HCC) – Suspected/Diagnosis
    ONC-14.3: Hepatocellular Carcinoma (HCC) – Initial Work-up/Staging
    ONC-14.4: Hepatocellular Carcinoma (HCC) – Restaging/Recurrence
    ONC-14.5: Hepatocellular Carcinoma (HCC) – Surveillance/Follow-up
    ONC-14.6: Gallbladder and Biliary Tumors – Initial Work-up/Staging
    ONC-14.7: Gallbladder and Biliary Tumors – Restaging/Recurrence
    ONC-14.8: Gallbladder and Biliary Tumors – Surveillance/Follow-up
    ONC-14.9: Gastric Cancer – Initial Work-up/Staging
    ONC-14.10: Gastric Cancer – Restaging/Recurrence
    ONC-14.11: Gastric Cancer – Surveillance/Follow-up

    ONC-14.1: Hepatocellular Carcinoma (HCC) – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Diagnosis: A biopsy is not always required for the diagnosis of Hepatocellular carcinoma (HCC). A dedicated triple-phase CT or MRI may be obtained. MRI with contrast is the test of choice for the evaluation of liver masses and offers soft tissue contrast resolution superior to CT as well as the possibility of using two different contrast agents, one of which if more blood flow based and the other which also is blood flow based and demonstrates hepatobiliary function (Eovist).Classical imaging findings include:

      ® Arterial phase hyperenhancement
      ® Venous phase washout appearance
      ® Capsule appearance
      ® Threshold growth

    For members who are high risk for developing HCC (cirrhosis, chronic Hepatitis B or current or prior HCC), if the liver lesion is > 1 cm with 2 classic enhancements on triple-phase CT or MRI, the diagnosis is confirmatory and biopsy is not needed.

    For lesions less than 1 cm or with less than 2 classical enhancements or for any liver lesions in members who are not high risk, a biopsy is needed for histological confirmation.

    PET/CT scan is not indicated for diagnosis or staging of Hepatocellular carcinoma


    ONC-14.2: Hepatocellular Carcinoma (HCC) - Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-26: Cirrhosis and Liver Screening for Hepatocellular Carcinoma

    See Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-29: Liver Lesion Characterization

    ONC-14.3: Hepatocellular Carcinoma (HCC) – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All members® CT Chest with contrast (CPT® 71260)

    One of the following:
    ® CT Abdomen with contrast (CPT® 74160)
    ® CT Abdomen without and with contrast (CPT® 74170)
    ® CT Abdomen and Pelvis with contrast (CPT® 74177) or without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast



    ONC-14.4: Hepatocellular Carcinoma (HCC) – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    One of the following:
    ® After initial therapy
    ® For suspected recurrence or new liver lesions
    ® Individuals receiving systemic therapy (every 2 cycles)
    ® CT Chest with contrast (CPT® 71260) or CT Chest without contrast (CPT® 71250)

    One of the following:
    ® CT Abdomen with contrast (CPT® 74160)
    ® CT Abdomen without and with contrast (CPT® 74170)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast

    Hepatocellular Carcinoma treated with embolization® CTA Abdomen (CPT® 74175) can be approved immediately prior to embolization

    One of the following, immediately prior to and 1 month post-ablation:
    ® MRI Abdomen without and with contrast (CPT® 74183)
    ® CT Abdomen without and with contrast (CPT® 74170)

    See also ONC-31.2 for imaging studies indicated prior to and post-embolization

    Hepatocellular Carcinoma awaiting liver transplant® See Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-42.1: Liver Transplant, Pre-Transplant for imaging guidelines

    ONC-14.5: Hepatocellular Carcinoma (HCC) – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Hepatocellular Carcinoma:
    ® Treated with surgical resection
    ® Treated with embolization
    Every 3 months for 2 years, then annually:
    ® CT Chest with contrast (CPT® 71260) or CT Chest without contrast (CPT® 71250)

    And ONE of the following:
    ® CT Abdomen with contrast (CPT® 74160)
    ® CT Abdomen without and with contrast (CPT® 74170)
    ® CT Abdomen and Pelvis with contrast (CPT® 74177) or without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast

    Hepatocellular Carcinoma treated with liver transplant® See Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-42.3: Liver Transplant, Post-transplant

    ONC-14.6: Gallbladder and Biliary Tumors – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All members® CT Chest with contrast (CPT® 71260)

    One of the following:
    ® CT Abdomen with contrast (CPT® 74160)
    ® CT Abdomen without and with contrast (CPT® 74170)
    ® CT Abdomen and Pelvis with contrast (CPT® 74177) or without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast

    Inconclusive findings on conventional imaging ® PET/CT (CPT® 78815)

    ONC-14.7: Gallbladder and Biliary Tumors – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Any of the following:
    ® After initial therapy
    ® For suspected recurrence or new liver lesions
    ® Members receiving systemic chemotherapy (every 2 cycles)
    ® CT Abdomen with contrast (CPT® 74160) or CT Abdomen without and with contrast (CPT® 74170) or MRI Abdomen without and with contrast (CPT® 74183)
    ® CT Chest with contrast (CPT® 71260) or CT Pelvis with contrast (CPT® 72193) may only be obtained for known disease or new signs/symptoms

    ONC-14.8: Gallbladder and Biliary Tumors – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All membersAnnually for 5 years:
    ® CT Chest with contrast (CPT® 71260) or CT Chest without contrast (CPT® 71250)

    And ONE of the following:
    ® CT Abdomen with contrast (CPT® 74160)
    ® CT Abdomen without and with contrast (CPT® 74170)
    ® CT Abdomen and Pelvis with contrast (CPT® 74177) or without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast
    Biliary carcinoma treated with liver transplantSee Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-42.3: Liver Transplant, Post-transplant


    ONC-14.9: Gastric Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All members® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    Gastric cancer ≥ T2 or higher with no metastatic disease by conventional imaging® PET/CT (CPT® 78815)

    ONC-14.10: Gastric Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    After initial therapy and any suspected recurrence ® CT Chest (CPT® 71260 ) and CT Abdomen/Pelvis with contrast (CPT® 74177)
    New liver lesion(s) and primary site controlled ® CT Abdomen (CPT® 74170) or MRI Abdomen without and with contrast (CPT® 74183)
    ® CT Chest with contrast (CPT® 71260)
    One of the following:
    ® After neoadjuvant therapy for presumed surgically resectable disease or
    ® Post curative chemoradiation being treated without surgery
    ® CT Chest (CPT® 71260 ) and CT Abdomen/Pelvis with contrast (CPT® 74177)
    Inconclusive findings on conventional imaging ® PET/CT (CPT® 78815)

    ONC-14.11: Gastric Cancer – Surveillance/Follow–up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Stage I (treated with resection alone)® No routine imaging unless clinical signs/symptoms of recurrence
    Any of the following:
    ® Stage I treated with systemic therapy
    ® Stages II-III
    ® Stage IV - Metastatic disease (post definitive treatment of all measurable disease or being observed off therapy)
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177) annually for 5 years


    References

    1. Ajani JA, D’Amico TA, Almhanna K et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – June 3, 2019. Gastric cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/gastric.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Gastric cancer V 2.2019– June 3, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org .
    2. Benson AB, D’Angelica MI, Abbot D et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – March 6, 2019. Hepatobiliary cancers, available at: https://www.nccn.org/professionals/physician_gls/pdf/hepatobiliary.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Hepatobiliary cancers, V 2.2019 – March 6, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org .
    3. Vallböhmer D, Hölscher AH, Schnieder PM, et al. [18F]-fluorodeoxyglucose-positron emission tomography for the assessment of histopathologic response and prognosis after completion of neoadjuvant chemotherapy in gastric cancer. J Surg Oncol. 2010;102(2):135-140. doi:10.1002/jso.21592.
    4. Zou H, Zhao Y. 18FDG PET-CT for detecting gastric cancer recurrence after surgical resection: a meta-analysis. Surg Oncol. 2013;22(3):162-166. doi:10.1016/j.suronc.2013.05.001.
    5. Bridgewater J, Galle PR, Khan SA, et al. Guidelines for the diagnosis and management of intrahepatic cholangiocarcinoma. J Hepatol. 2014;60(6):1268-1289. doi:10.1016/j.jhep.2014.01.021.
    6. Khan SA, Davidson BR, Goldin RD, et al. Guidelines for the diagnosis and treatment of cholangiocarcinoma: an update. Gut. 2012;61(12):1657-1669. doi:10.1136/gutjnl-2011-301748.
    7. Benson AB 3rd, D’Angelica MI, Abrams TA, et al. Hepatobiliary cancers, version 2.2014. J Natl Compr Canc Netw. 2014;12(8):1152-1182.

    ONC-15: Neuroendocrine Cancers and Adrenal Tumors

    ONC-15.1: General Considerations
    ONC-15.2: Gastrointestinal/Pancreatic Neuroendocrine Cancers – Suspected/Diagnosis
    ONC-15.3: Gastrointestinal/Pancreatic Neuroendocrine Cancers – Initial Work-up/Staging
    ONC-15.4: Gastrointestinal/Pancreatic Neuroendocrine Cancers – Restaging/Recurrence
    ONC-15.5: Gastrointestinal/Pancreatic Neuroendocrine Cancers – Surveillance
    ONC-15.6: Bronchopulmonary or Thymic Carcinoid – Initial Staging
    ONC-15.7: Bronchopulmonary or Thymic Carcinoid –Restaging/Recurrence
    ONC-15.8: Bronchopulmonary or Thymic Carcinoid – Surveillance
    ONC-15.9: Adrenal Tumors – Suspected/Diagnosis
    ONC-15.10: Adrenal Tumors – Initial Work-up/Staging
    ONC-15.11: Adrenal Tumors – Restaging/Recurrence
    ONC-15.12: Adrenal Tumors – Surveillance
    ONC-15.13: Adrenocortical Carcinoma


    ONC-15.1: General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    This guideline includes low-grade or well-differentiated carcinoid and endocrine tumors of the lung, thymus, pancreas, gastrointestinal tract or unknown primary site; including insulinoma, glucagonoma, VIPoma, gastrinoma, somatostatinoma and others as well as catecholamine-secreting tumors of the adrenal gland such as pheochromocytoma, paraganglioma, adrenocortical carcinoma, and others.

    For poorly-differentiated or high-grade small cell or large cell neuroendocrine tumors arising outside the lung or from an unknown primary site see: ONC-31.8: Extrathoracic Small Cell and Large Cell Neuroendocrine Tumors

    For poorly-differentiated or high grade neuroendocrine tumors of the lung, refer to ONC-7: Small Cell Lung Cancer

    Neuroblastoma, ganglioneuroblastoma, and ganglioneuroma occurring in adults should be imaged according to Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-6: Neuroblastoma

    Many are associated with Multiple Endocrine Neoplasia (MEN) familial syndromes. – See Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-2.8: Multiple Endocrine Neoplasias (MEN) for screening recommendations

    Somatostatin receptor-based imaging is more sensitive and specific for evaluation of well-differentiated neuroendocrine tumors and may be performed using 111In DTPA Octreotide scintigraphy or 68Gallium-labeled DOTATATE PET/CT scan. This study is not part of evaluation of poorly-differentiated or high grade neuroendocrine tumors, which are imaged according to: ONC-31.8: Extrathoracic Small Cell and Large Cell Neuroendocrine Tumors

    ONC-15.2: Gastrointestinal/Pancreatic Neuroendocrine Cancers – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ® Systemic symptoms strongly suggestive of functioning neuroendocrine tumor
    ® Suspicious findings on other imaging studies
    ® Unexplained elevation in any of the following:
      ¡ Chromogranin A
      ¡ 5HIAA
      ¡ Insulin
      ¡ VIP
      ¡ Glucagon
      ¡ Gastrin
      ¡ Substance P
      ¡ Serotonin
      ¡ Somatostatin
    Any or all of the following:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) or without and with contrast (CPT® 74178)
      ¡ If CT inconclusive, MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast is indicated
    ® CT Chest with contrast (CPT® 71260) or CXR
    ® Continued suspicion with negative/inconclusive CT scan or MRIONE of the following:
    ® CPT® 78802 – whole body single day study (Octreotide scan) OR
    ® CPT® 78804 whole body two or more day study (Octreotide scan) OR
    ® CPT® 78830, 78831, or 78832 (SPECT/CT) OR
      ¡ CPT® 78803 (SPECT) may be approved as an add-on test to any one of the above codes
    ® 68Gallium-labeled DOTATATE PET/CT scan (CPT® 78815)
    ONC-15.3: Gastrointestinal/Pancreatic Neuroendocrine Cancers – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Carcinoid, pancreatic neuroendocrine tumors If not already done:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) or without and with contrast (CPT® 74178)
      ¡ If CT inconclusive, MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast is indicated
    ® CT Chest with contrast (CPT® 71260)
    Inconclusive CT or MRI scansONE of the following:
    ® CPT® 78802 – whole body single day study (Octreotide scan) OR
    ® CPT® 78804 whole body two or more day study (Octreotide scan) OR
    ® CPT® 78830, 78831, or 78832 (SPECT/CT) OR
      ¡ CPT® 78803 (SPECT) may be approved as an add-on test to any one of the above codes
    ® 68Gallium-labeled DOTATATE PET/CT scan (CPT® 78815)
    Any of the following:
    ® Markers fail to normalize after complete resection AND CT/MRI and somatostatin-receptor based study are negative
    ® Biopsy-proven neuroendocrine tumor of unknown primary site AND CT/MRI and somatostatin-receptor based study are negative
    ® FDG-PET/CT scan (CPT® 78815)
    ONC-15.4: Gastrointestinal/Pancreatic Neuroendocrine Cancers – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All after surgical resection® See: Surveillance below
    Unresectable/metastatic disease on treatment with somatostatin analogues ® CT of involved body area no more frequently than every 3 months
    Unresectable/metastatic disease on treatment with chemotherapy ® CT of involved body area every 2 cycles (6 to 8 weeks)
    Progression of symptoms or elevation of tumor markers® CT Chest without (CPT® 71250) or CT Chest with contrast (CPT® 71260)

    ONE of the following:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast

    Continued suspicion for recurrence with negative or inconclusive CT scan or MRIONE of the following:
    ® CPT® 78802 – whole body single day study (Octreotide scan) OR
    ® CPT® 78804 whole body two or more day study (Octreotide scan) OR
    ® CPT® 78830, 78831, or 78832 (SPECT/CT) OR
    ¡ CPT® 78803 (SPECT) may be approved as an add-on test to any one of the above codes
    ® 68Gallium-labeled DOTATATE PET/CT scan (CPT® 78815)
    To assess candidacy for peptide receptor radionuclide therapy (PRRT) with Lutetium 177Lu-dotatateONE of the following:
    ® Octreotide scan (either CPT® 78802 – whole body single day study OR CPT® 78804 - whole body two or more day study).
      ¡ CPT® 78803 (SPECT) may be approved as an add-on test to any one of the above codes
    ® 68Gallium-labeled DOTATATE PET/CT scan (CPT® 78815)

    ONC-15.5: Gastrointestinal/Pancreatic Neuroendocrine Cancers – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Any of the following:
    ® Appendix carcinoid ≤2 cm, completely resected
    ® Rectal carcinoid <1 cm, completely resected
    ® Advanced imaging is not routinely indicated for surveillance
    Rectal carcinoid 1-2 cm, completely resected® MRI Pelvis (CPT® 72197) without and with contrast once at 12 months post resection. If clear, no further surveillance imaging indicated
    All other neuroendocrine tumors of the bowel (small/large)® CT Abdomen/Pelvis (CPT® 74177) once at 3 to 12 months postoperatively and annually for 3 years and then every 2 years up to year 10
    Neuroendocrine tumors of the upper abdomen (i.e., pancreas, stomach)® CT Abdomen (CPT® 74160) once at 3 to 12 months postoperatively then annually for 3 years and then every 2 years up to 10
    ONC-15.6: Bronchopulmonary or Thymic Carcinoid – Initial Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Initial diagnosisIf not already done:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) or without and with contrast (CPT® 74178)
      ¡ If CT inconclusive, MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast is indicated
    Inconclusive CT or MRI scansONE of the following:
    ® CPT® 78802 – whole body single day study (Octreotide scan) OR
    ® CPT® 78804 whole body two or more day study (Octreotide scan) OR
    ® CPT® 78830, 78831, or 78832 (SPECT/CT) OR
      ¡ CPT® 78803 (SPECT) may be approved as an add-on test to any one of the above codes
    ® 68Gallium-labeled DOTATATE PET/CT scan (CPT® 78815)
    Any of the following:
    ® Markers fail to normalize after complete resection AND CT/MRI and somatostatin-receptor based study are negative
    ® Biopsy-proven neuroendocrine tumor of unknown primary site AND CT/MRI and somatostatin-receptor based study are negative
    ® FDG- PET/CT scan (CPT® 78815)
    ONC-15.7: Bronchopulmonary or Thymic Carcinoid – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All after surgical resection® See: Surveillance below
    Unresectable/metastatic disease on treatment with somatostatin analogues® CT of involved body area no more frequently than every 3 months
    Unresectable/metastatic disease on treatment with chemotherapy® CT of involved body area every 2 cycles (6 to 8 weeks)
    Progression of symptoms or elevation of tumor markers® CT Chest without (CPT® 71250) or CT Chest with contrast (CPT® 71260)

    ONE of the following:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast

    Continued suspicion for recurrence with negative or inconclusive CT scan or MRIONE of the following:
    ® CPT® 78802 – whole body single day study (Octreotide scan) OR
    ® CPT® 78804 whole body two or more day study (Octreotide scan) OR
    ® CPT® 78830, 78831, or 78832 (SPECT/CT)
      ¡ CPT® 78803 (SPECT) may be approved as an add-on test to any one of the above codes
    ® 68Gallium-labeled DOTATATE PET/CT scan (CPT® 78815)
    ONC-15.8: Bronchopulmonary or Thymic Carcinoid – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Carcinoid tumors of lung or thymus® CT Chest with contrast (CPT® 71260) or CT Chest without contrast (CPT® 71250) once at 3 to 12 months post resection and then annually for 3 years and then every 2 years up to year 10
    ONC-15.9: Adrenal Tumors – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-16: Adrenal Cortical Lesions for imaging guidelines for evaluation of suspected adrenal malignancies

    If concern for genetic predisposition syndrome such as MEN, neurofibromatosis, or Von Hippel-lindau disease, see screening recommendations in Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-2: Screening Imaging and Cancer Predisposition Syndromes.

    ONC-15.10: Adrenal Tumors – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    For any of the following:
    ® Pheochromocytoma
    ® Paraganglioma
    ® Paraganglioneuroma
    If not already done:
    ® CT Chest without (CPT® 71250) or CT Chest with contrast (CPT® 71260)

    One of the following (if not already done):
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast

    Continued suspicion with negative/inconclusive CT scan or MRIONE of the following:
    ® MIBG Scan (either CPT® 78802 – whole body single day study OR CPT® 78804 - whole body two or more day study).
      ¡ CPT® 78803 (SPECT) may be approved as an add-on test to any one of the above codes
    ® Octreotide scan (either CPT® 78802 – whole body single day study OR CPT® 78804 - whole body two or more day study).
      ¡ CPT® 78803 (SPECT) may be approved as an add-on test to any one of the above codes
    ® 68Gallium-labeled DOTATATE PET/CT scan (CPT® 78815)
    All above studies done and negative/inconclusive ® FDG-PET/CT scan (CPT® 78815)
    ONC-15.11: Adrenal Tumors – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    If surgery is primary therapy® CT Abdomen (CPT® 74160) one time within first year post resection then go to surveillance recommendations
    Recurrence, progression of symptoms, or elevation of tumor markers® CT Chest without (CPT® 71250) or CT Chest with contrast (CPT® 71260)

    ONE of the following:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast

    Continued suspicion for recurrence with negative or inconclusive CT scan or MRIONE of the following:
    ® MIBG scan (either CPT® 78802 – whole body single day study OR CPT® 78804 - whole body two or more day study).
      ¡ CPT® 78803 (SPECT) may be approved as an add-on test to any one of the above codes
    ® SPECT/CT CPT® 78830, CPT® 78831, or CPT® 78832
    ® Octreotide scan (either CPT® 78802 – whole body single day study OR CPT® 78804 - whole body two or more day study).
      ¡ CPT® 78803 (SPECT) may be approved as an add-on test to any one of the above codes
    ® 68Gallium-labeled DOTATATE PET/CT scan (CPT® 78815)
    All above studies done and negative/ inconclusive ® FDG-PET/CT scan (CPT® 78815)

    ONC-15.12: Adrenal Tumors – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All members® CT Abdomen with contrast (CPT® 74160) and CT of other involved body areas with contrast annually for 10 years
    ONC-15.13: Adrenocortical Carcinoma

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Initial Staging® CT Chest without (CPT® 71250) or CT Chest with contrast (CPT® 71260)

    One of the following (if not already done):
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast

    Suspected recurrence® CT Chest without (CPT® 71250) or CT Chest with contrast (CPT® 71260)

    ONE of the following:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast

    Surveillance® CT Abdomen with contrast (CPT® 74160) and CT of other involved body areas with contrast annually for 5 years


    References

    1. Kulke MH, Shah MH, Benson AB, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2019 – March 5, 2019. Neuroendocrine tumors, available at: https://www.nccn.org/professionals/physician_gls/pdf/neuroendocrine.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Neuroendocrine tumors V 1.2019 – March 5 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Qadan M, Ma Y, Visser BC, et al. Reassessment of the current American Join Committee on Cancer staging system for pancreatic neuroendocrine tumors. J Am Coll Surg. 2014;218(2):188-195. doi:10.1016/j.jamcollsurg.2013.11.001.
    3. Lenders JWM, Duh Q-Y, Eisenhofer G, et al. Pheochromocytoma and paraganglioma: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2014;99(6):1915-1942. doi:10.1210/jc.2014-1498.
    4. Ruys AT, Bennink RJ, van Westreenen HL, et al. FDG-positron emission tomography/computed tomography and standardized uptake value in the primary diagnosis and staging of hilar cholangiocarcinoma. HPB (Oxford). 2011;13(4):256-262. doi: 10.1111/j.1477-2574.2010.00280.x.
    5. Ter-Minassian M, Chan JA, Hooshmand SM, et al. Clinical presentation, recurrence, and survival in patients with neuroendocrine tumors: results from a prospective institutional database. Endocr Relat Can. 2013;20(2):187-196. doi:10.1530/ERC-12-0340.
    6. Murray SE, Lloyd RV, Sippel RS, Chen H, Oltmann SC. Postoperative surveillance of small appendiceal carcinoid tumors. Am J Surg. 2014;207(3):342-345. doi:10.1016/j.amjsurg.2013.08.038.
    7. Thakker RV, Newey PJ, Walls GV, et al. Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1). J Clin Endocrinol Metab. 2012;97(9):2990-3011. doi:10.1210/jc.2012-1230.
    8. Singh S, Moody L, Chan DL, et al. Follow-up recommendations for completely resected gastroenteropancreatic neuroendocrine tumors. JAMA Oncol. 2018;4(11):1597-1604. doi:10.1001/jamaoncol.2018.2428.

    ONC-16: Colorectal Cancer

    ONC-16.0: Colorectal Cancer – General Considerations
    ONC-16.1: Colorectal Cancer – Suspected/Diagnosis
    ONC-16.2: Colorectal Cancer – Initial Work-up/Staging
    ONC-16.3: Colorectal Cancer – Restaging/Recurrence
    ONC-16.4: Colorectal Cancer – Surveillance/Follow-up

    ONC-16.0: Colorectal Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Duodenal and small bowel adenocarcinoma follows imaging guidelines for colorectal cancer.

    Neuroendocrine tumors of the bowel are covered in: ONC-15: Neuroendocrine Cancers and Adrenal Tumors

    Appendiceal adenocarcinoma (including pseudomyxoma peritonei) follows imaging guidelines for colorectal cancer

    ONC-16.1: Colorectal Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-22: GI Bleeding or Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-25: CT Colonography (CTC) for imaging guidelines for evaluation of suspected colorectal malignancies

    ONC-16.2: Colorectal Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Carcinoma within a polyp that is completely removed® No advanced imaging needed
    Invasive adenocarcinoma® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    Further evaluation of an inconclusive liver lesion seen on CT ® MRI Abdomen without and with contrast (CPT® 74183)
    One of the following:
    ® Isolated metastatic lesion(s) on other imaging and member is a candidate for aggressive surgical resection or other localized treatment to metastasis for curative intent
    ® Inconclusive conventional imaging
    ® PET/CT (CPT® 78815)
    Rectal adenocarcinomaIn addition to above, for preoperative planning:
    ® Endorectal ultrasound (CPT® 76872)
    ® MRI Pelvis without and with contrast (CPT® 72197)

    ONC-16.3: Colorectal Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Complete resection® See Surveillance below
    Recurrence suspected® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    After completion of planned neoadjuvant therapyMembers without metastatic disease, when requested by operating surgeon for operative planning:
    ® CT with contrast or MRI without and with contrast of all operative sites

    All other members:
    ® No advanced imaging since surgery is “planned”

    Unresected primary disease or metastatic disease on chemotherapyEvery 2 cycles of chemotherapy treatment and at the completion of chemoradiotherapy:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of other involved or symptomatic areas
    Further evaluation of an inconclusive liver lesion seen on CT ® MRI Abdomen without and with contrast (CPT® 74183)
    One of the following:
    ® Postoperative elevated or rising CEA or LFTs with negative recent conventional imaging
    ® Isolated metastatic lesion(s) on other imaging and member is a candidate for aggressive surgical resection or other localized treatment to metastasis for curative intent
    ® Differentiate local tumor recurrence from postoperative and/or post-radiation scarring
    ® PET/CT (CPT® 78815)
    New or worsening pelvic pain and recent CT imaging negative or inconclusive® MRI Pelvis without and with contrast (CPT® 72197)
    ONC-16.4: Colorectal Cancer – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging/Lab Study
    Colon and rectal adenocarcinoma:
    ® Stage I
    ® No routine advanced imaging indicated
    Colon and rectal adenocarcinoma:
    ® Stage II-III
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast after completion of surgery and then annually for 5 years
    Colon and rectal adenocarcinoma:
    ® Stage IV - Metastatic disease (post definitive treatment of all measurable disease or being observed off therapy)
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast every 6 months for 2 years and then annually for 3 years
    Rectal cancer treated with transanal excision alone® Endorectal ultrasound (CPT® 76872) every 6 months for 5 years
    ® MRI Pelvis without and with contrast (CPT® 72197) for abnormal findings on ultrasound or new signs/symptoms concerning for local recurrence
    Pseudomyxoma peritoneiOne of each of the following, every 3 months for first year, then every 6 months for 4 more years:
    ® CT Chest with (CPT® 71260) or CT Chest without contrast (CPT® 71250)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) or MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast


    References

    1. Benson AB, Venook AP, Cederquist L, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – May 15, 2019. Colon cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/colon.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Colon cancer V 2.2019 – May 15, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Benson AB, Venook AP, Cederquist L, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – May 15, 2019. Rectal cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/rectal.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Rectal cancer V 2.2019 - May 15, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    3. ACR Appropriateness Criteria. Pretreatment Staging of Colorectal Cancer. Rev. 2011.
    4. Bailey CE, Hu C-Y, You YN et al. Variation in positron emission tomography use after colon cancer resection. J Oncol Pract. 2015;11(3):e363-e372. doi:10.1200/JOP.2014.001933.
    5. Lu YY, Chen JH, Ding HJ, Chien CR, Lin WY, Kao CH. A systematic review and meta-analysis of pretherapeutic lymph node staging of colorectal cancer by 18F-FDG PET or PET/CT. Nucl Med commun. 2012;33(11):1127-1133. doi:10.1097/MNM0b013e328357b2d9.
    6. Moulton CA, Gu CS, Law CH, et al. Effect of PET before liver resection on surgical management for colorectal adenocarcinoma metastases: a randomized clinical trial. JAMA. 2014;311(18):1863-1869. doi:10.1001/jama.2014.3740.
    7. Steele SR, Chang GJ, Hendren S, et al. Practice guideline for the surveillance of patients after curative treatment of colon and rectal cancer. Dis Colon Rectum. 2015;58(8):713-725. doi:10.1097/DCR.0000000000000410.
    8. van de Velde CJ, Boelens PG, Borras JM, et al. EURECCA colorectal: multidisciplinary management: European concensus conference colon & rectum. Eur J Cancer. 2014;50(1):e1-e34. doi:10.1016/j.ejca.2013.06.048.


    ONC-17: Renal Cell Cancer (RCC)

    ONC-17.0: Renal Cell Cancer (RCC) – General Considerations
    ONC-17.1: Renal Cell Cancer (RCC) – Suspected/Diagnosis
    ONC-17.2: Renal Cell Cancer (RCC) – Initial Work-up/Staging
    ONC-17.3: Renal Cell Cancer (RCC) – Restaging/Recurrence
    ONC-17.4: Renal Cell Cancer (RCC) – Surveillance

    ONC-17.0: Renal Cell Cancer (RCC) – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    PET is not routinely indicated for initial diagnosis, staging or restaging of renal cell cancer.

    Data is lacking on improvements in outcomes of renal cell cancer survivors based upon surveillance imaging schedules.

    A minority of adult members with renal cell cancer (RCC) will have translocations in TFE3 or TFEB, which have a different natural history than “adult type” RCC. Members of any age with TFE3 or TFEB translocated RCC should be imaged according to guidelines in Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-7.4: Pediatric Renal Cell Carcinoma (RCC).

    Members of any age with Wilms tumor should be imaged according to guidelines in section Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-7.2: Unilateral Wilms Tumor (UWT) or Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-7.3 Bilateral Wilms Tumor (BWT).

    ONC-17.1: Renal Cell Cancer (RCC) – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ® Solitary renal mass suspicious for renal cell cancer® See AB-35: Indeterminate Renal Lesion for imaging guidelines for evaluation of suspected renal malignancies
    ® Chest x-ray
    ® CT chest with contrast with (CPT® 71260) or without contrast (CPT® 71250) may be obtained for one of the following:
      ¡ New chest x-ray abnormalities
      ¡ Pulmonary symptoms
      ¡ Histologically confirmed renal cell cancer

    ONC-17.2: Renal Cell Cancer (RCC) – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All membersIf not done previously:
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ® CT Abdomen/Pelvis, contrast as requested
    Any of the following:
    ® Extension of tumor into the vena cava by other imaging
    ® Inconclusive findings on CT
    ® MRI Abdomen without and with contrast (CPT® 74183)
    Bone pain® Bone scan (See ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    Any of the following:
    ® Signs/symptoms of brain metastases
    ® IL-2 therapy being considered
    ® MRI Brain without and with contrast (CPT® 70553)

    ONC-17.3: Renal Cell Cancer (RCC) – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Unresectable disease or metastatic disease on systemic therapyEvery 2 cycles of treatment (commonly every 6 to 8 weeks):
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of other involved or symptomatic areas
    Recurrence suspected® CT Chest (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177)

    ONC-17.4: Renal Cell Cancer (RCC) – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Stage I RCC, on active surveillance of renal mass <1 cmOne of the following, once within 6 months of surveillance initiation and annually for 5 years:
    ® CT Abdomen without and with contrast (CPT® 74170)
    ® MRI (CPT® 74183) Abdomen without and with contrast
    ® Also see Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-35.1: Indeterminate Renal Lesion
    Stage I RCC, on active surveillance of renal mass ≥1 cmOne of the following, every 3 months for year 1, every 6 months for years 2 and 3 and annually thereafter:
    ® CT Abdomen without and with contrast (CPT® 74170)
    ® MRI Abdomen without and with contrast (CPT® 74183)
    Stage I or II RCC, post-ablation therapyOne of the following, at 3 and 6 months post-ablation and then annually for 5 years:
    ® CT Abdomen without and with contrast (CPT® 74170)
    ® MRI Abdomen without and with contrast (CPT® 74183)
    Stage I RCC, after partial or radical nephrectomyOne of each of the following, 3 to 12 months post-resection:
    ® CT Chest with (CPT® 71260) or without contrast (CPT® 71250)
    ® CT Abdomen with (CPT® 74160) or CT Abdomen without contract (CPT® 74150) or MRI Abdomen without and with contrast (CPT® 74183)

    Annually for 3 years:
    ® Chest x-ray or CT Chest with (CPT® 71260) or CT Abdomen without (CPT® 71250) contrast
    ® Abdominal imaging with any ONE of the following:

      ¡ Abdominal ultrasound (CPT® 76770 or CPT® 76775)
      ¡ CT Abdomen with (CPT® 74160) or CT Abdomen without (CPT® 74150) contrast
      ¡ MRI Abdomen without and with contrast (CPT® 74183)
    Stage II RCC, post-nephrectomyOne of each of the following, 3 to 6 months post-resection:
    ® CT Chest with (CPT® 71260) or CT Chest without contrast (CPT® 71250)
    ® CT Abdomen with (CPT® 74160) or CT Abdomen without (CPT® 74150) contrast or MRI Abdomen without and with contrast (CPT® 74183)

    One of each of the following, every 6 months for 3 years, then annually to year 5:
    ® Chest x-ray or CT Chest with (CPT® 71260) or without (CPT® 71250) contrast
    ® Abdominal imaging with any ONE of the following:

      ¡ Abdominal ultrasound (CPT® 76770 or CPT® 76775)
      ¡ CT Abdomen with (CPT® 74160) or CT Abdomen without (CPT® 74150) contrast
      ¡ MRI Abdomen without and with contrast (CPT® 74183)
    Any of the following:
    ® Stage III RCC, post-nephrectomy
    ® Stage IV RCC, not receiving therapy, no measurable disease
    One of each of the following, 3 to 6 months post-resection:
    ® CT Chest with (CPT® 71260) or CT Chest without contrast (CPT® 71250)
    ® CT Abdomen with (CPT® 74160) or CT Abdomen without contrast (CPT® 74150) or MRI Abdomen without and with contrast (CPT® 74183)

    One of each of the following, every 3 months for 3 years, then annually to year 5:
    ® CT Chest with (CPT® 71260) or CT Chest without contrast (CPT® 71250)
    ® CT Abdomen with (CPT® 74160) or CT Abdomen without contrast (CPT® 74150) or MRI Abdomen without and with contrast (CPT® 74183)

    Metastatic disease on a break from therapy with persistent measurable diseaseAny or all of the following, every 3 months:
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® CT with contrast of other involved or symptomatic areas


    References

    1. Motzer RJ, Jonasch E, Agarwal N, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2020 – June 7, 2019. Kidney cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/kidney.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Kidney cancer V 1.2020 – June 7, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. ACR Appropriateness Criteria. Post-treatment follow up of renal cell carcinoma. Rev. 2013.
    3. Donat SM, Diza M, Bishoff JF, et al. Follow up for clinically localized renal neoplasms: AUA guideline. J Urol. 2013;190(2):406-416. doi:10.1016/j.juro/2014.04.121.
    4. Herts BR, Silverman SG, Hindman NM, et al. Management of the incidental renal mass on CT: a white paper of the ACR incidental findings committee. J Am Coll Radiol. 2018;15(2):264-273. doi:10.1016/j.jacr.2017.04.028.
    5. Finelli A, Ismaila N, Bro B, et al. Management of small renal masses. American Society of Clinical Oncology clinical practice guideline. Journal of Clinical Oncology. 2017;35(6):668-680. doi:10.1200/JCO.2016.69.9645.
    6. Davenport MS, Caoili EM, Cohan RH, et al. MRI and CT characteristics of successfully ablated renal masses: imaging surveillance after radiofrequency ablation. AJR Am J Roentgenol. 2009;192:1571-1578. doi:10.2214/AJR.08.1303.
    7. Clark TW, Millward SF, Gervais DA, et al. Reporting standards for percutaneous thermal ablation of renal cell carcinoma. J Vasc Interv Radiol. 2009;20(7 Suppl):S409-S416. doi:10.1016/j.jvir.2009.04.013.
    8. Rais-Bahrami S, Guzzo TJ, Jarrett TW, Kavoussi LR, Allaf ME. Incidentally discovered renal masses: oncological and perioperative outcomes in patients with delayed surgical intervention. BJU Int. 2009;103(10):1355-1358. doi:10.1111/j.1464-410X.2008.08242.x.
    9. Wang HY, Ding HJ, Chen JH, Chao CH, Lu YY, Lin WY, Kao CH. Meta-analysis of the diagnostic performance of [18F]FDG-PET and PET/CT in renal cell carcinoma. Cancer Imaging. 2012 October;12:464-474. doi:10.1102/1470-7330.2012.0042.
    10. Kim EH, Strope SA. Postoperative surveillance imaging for patients undergoing nephrectomy for renal cell carcinoma. Urol Oncol. 2015;33(12):499-502. doi:10.1016/j.urolonc.2015.08.008.
    11. Sankineni S, Brown A, Cieciera M, Choyke PL, Turkbey B. Imaging of renal cell carcinoma. Urol Oncol. 2016;34(3):147-155. doi:10.1016/j.urolonc.2015.05.020.
    12. ACR Appropriateness Criteria. Renal cell carcinoma staging. Rev. 2015.



    ONC-18: Transitional Cell Cancer

    ONC-18.0: Transitional Cell Cancer – General Considerations
    ONC-18.1: Transitional Cell Cancer – Suspected/Diagnosis
    ONC-18.2: Transitional Cell Cancer – Initial Work-up/Staging
    ONC-18.3: Transitional Cell Cancer – Restaging/Recurrence
    ONC-18.4: Transitional Cell Cancer – Surveillance/Follow-up

    ONC-18.0: Transitional Cell Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Transitional cell cancers can include: tumors of the bladder, ureters, prostate, urethra, or renal pelvis. For primary cancer of the kidney, see ONC-17: Renal Cell Cancer (RCC).

    Most common histology of bladder cancer is transitional cell (TCC) or urothelial carcinoma (UCC). Rare histologies include squamous cell (imaged according to ONC-18: Transitional Cell Cancer) or small cell (imaged according to ONC-31.8: Extrathoracic Small Cell and Large Cell)

    Urachal cancer is rare type of bladder cancer; the most common histology is adenocarcinoma. These are imaged according to muscle invasive bladder cancer.

    PET not routinely indicated in transitional cell cancer with exception noted below in ONC-18.2: Transitional Cell Cancer – Initial Work-up/Staging

    ONC-18.1: Transitional Cell Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-39: Hematuria and Hydronephrosis for imaging guidelines for evaluation of suspected transitional cell malignancies

    ONC-18.2: Transitional Cell Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All membersOne of the following:
    ® CT Abdomen/Pelvis without and with contrast (CPT® 74178)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast if contraindication to CT contrast
    ® CT Abdomen/Pelvis without contrast (CPT® 74176) with retrograde pyelogram or renal ultrasound (CPT® 76770 or CPT® 76775) in members who cannot receive either CT or MRI contrast
    Any of the following:
    ® Muscle invasive bladder carcinoma
    ® Urethral carcinoma
    ® Urothelial carcinoma of the prostate
    ® CT Chest without (CPT® 71250) or with contrast (CPT® 71260)
    Members without metastatic disease, when requested by operating surgeon for operative planning® CT with contrast or MRI without and with contrast of all operative sites
    To evaluate inconclusive findings on conventional imaging® PET/CT (CPT® 78815)
    ONC-18.3: Transitional Cell Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Any stage > T1 or treated with definitive surgery® “Baseline” CT Abdomen/Pelvis with contrast (CPT® 74177) after surgery if requested
    Recurrence suspicion® CT Abdomen/Pelvis with contrast (CPT® 74177) or with and without contrast (CPT® 74178)
    ® CT Chest with contrast (CPT® 71260) if abnormal chest x-ray or lung nodules seen on other imaging
    After neoadjuvant therapy and before resection® CT Chest with contrast (CPT® 71260) and CT Urogram (CPT® 74178)
    Monitoring therapy for metastatic diseaseEvery 2 cycles of therapy:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Chest with contrast (CPT® 71260) if prior involvement or abnormal chest x-ray

    ONC-18.4: Transitional Cell Cancer – Surveillance/Follow-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Any of the following:
    ® Low grade lesions
    ® High grade Ta lesion ≤ 3 cm
    ® Papillary urothelial neoplasm of low malignant potential
    ® Advanced imaging is not routinely indicated for surveillance
    Any of the following:
    ® Recurrent high grade Ta lesions
    ® Superficial and minimally invasive (Tis and T1) transitional cell carcinoma of the bladder or upper tracts
    ® CT Urogram (CPT® 74178) every 2 years for 10 years
    Minimally invasive transitional carcinoma of the bladder treated with cystectomy® CT urogram (CPT® 74178) at 3 months post-cystectomy, and then annually for 5 years
    Muscle invasive lower and upper genitourinary tumors ® CT Abdomen/Pelvis with contrast (CPT® 74177) or without and with contrast (CPT® 74178) every 6 months for 2 years, then annually for 3 more years
    ® Chest x-ray
    Urethral cancers (high risk T1 or greater) and urothelial carcinoma of the prostate® CT Abdomen/Pelvis with contrast (CPT® 74177) or MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast every 6 months for 2 years and then annually
    ® Chest x-ray

    References

    1. Spiess PE, Agarwal N, Bangs R, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 3.2019 – April 23, 2019. Bladder cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/bladder.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Bladder cancer V 3.2019 – April 23, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Verma S, Rajesh A, Prasad SR et al, Urinary bladder cancer: role of MR imaging. Radiographics. 2012;32(2):371-387. doi:10.1148/rg.322115125.
    3. Lu YY, Chen JH, Liang JA. Clinical value of FDG PET or PET/CT in urinary bladder cancer: a systematic review and meta-analysis. Eur J Radiol. 2012;81(9):2411-2416. doi:10.1016/j.ejrad.2011.07.018.
    4. Witjes JA, Comperat E, Cowan NC, et al. EAU guidelines on muscle-invasive and metastatic bladder cancer: summary of the 2013 guidelines. Eur Urol. 2014;65(4):778-792. doi:10.1016/j.eururo.2013.11.046.
    5. Gakis G, Witjes JA, Comperat E, et al. EAU guidelines on primary urethral carcinoma. Eur Urol. 2013;64(5):823-830. doi:10.1016/j.eururo.2013.03.044.
    6. Rouprêt M, Babjuk M, Compérat E, et al. European guidelines on upper tract urothelial carcinomas: 2013 update. Eur Urol. 2013;63(6):1059-1071. doi:10.1016/j.eururo.2013.03.032.

    ONC-19: Prostate Cancer

    ONC-19.0: Prostate Cancer – General Considerations
    ONC-19.1: Suspected Prostate Cancer
    ONC-19.2: Prostate Cancer – Initial Work-up/Staging
    ONC-19.3: Prostate Cancer – Restaging/Recurrence
    ONC-19.4: Prostate Cancer – Follow-up On Active Surveillance
    ONC-19.5: Surveillance/Follow-up For Treated Prostate Cancer

    ONC-19.0: Prostate Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    The natural history of prostate cancer is highly variable. Therapeutic options may include surgery and radiation therapy along with Active Surveillance (also called expectant management or deferred treatment).

    When working up members with suspected new or recurrent prostate cancer, MRI should not be used to make a decision not to biopsy5. If the clinical suspicion is high enough, biopsy must be performed.

    PET/CT scan using 18F-FDG and 18F-Na Fluoride radiotracers is considered investigational for all indications for prostate cancer.

    PET/CT scan using newer radiotracers such as 11C Choline and 18F-Fluciclovine (AXUMIN®) have emerging data in restaging previously treated prostate cancer. Performance of these PET/CT scans in detecting early recurrence is poor at low PSA values of <2 ng/mL. False positive rate is high and histological confirmation of positive sites is recommended. Hence, its use is restricted to the evaluation of a rising PSA after conventional imaging is negative. Coverage may vary with individual health care plan.

      ® Additionally, while detection of low-volume recurrence after treatment of prostate cancer may influence therapeutic decisions; there is lack of evidence on how this approach has any meaningful impact on overall survival.

    As laser prostate ablation is considered investigational at this time, advanced imaging for treatment planning and/or surveillance of laser prostate ablation is not indicated.

    As high intensity focused ultrasound prostate ablation is considered investigational at this time, and advanced imaging for treatment planning and/or surveillance of high intensity focused ultrasound prostate ablation is not indicated.

    MR Spectroscopy (CPT® 76390) is considered investigational in the evaluation of prostate cancer at this time.

    Based on the local extent of tumor, PSA level and Gleason score, prostate cancer members can be classified into risk groups as below:
    Prostate Cancer – Risk Categories
    Risk Category
    T stage
    Gleason score
    PSA (ng/ml)
    Very lowT1c≤ 6< 10
    LowT1-T2a≤ 6< 10
    IntermediateT2b-T2c710-20
    HighT3a8 to 10> 20
    Very HighT3b-T48 to 10> 20
    3D Rendering of MRI for MRI / Ultrasound Fusion Biopsy:

    When specific target lesion(s) is (are) detected on mpMRI prostate and classified as PIRADS 4 or 5, then 3D Rendering at independent workstation (CPT® 76377, 3D rendering requiring image post-processing on an independent workstation) for the radiologist to generate prostate segmentation data image set for target identification on MRI/TRUS fusion biopsy is approvable either as subsequent separate standalone request or as retrospective request for medical necessity.

    If there is no target lesion identified on MRI then 3D rendering and MRI/TRUS fusion biopsy is not generally indicated. The urologist may request MRI/TRUS fusion biopsy of a PIRADS 1-3 lesion. Then approval of 3D rendering at independent workstation (CPT® 76377) can be considered on a case-by-case basis. These cases should be referred for Medical Director review.

    The 3D rendering for the TRUS component of the fusion is a part of the UroNav Fusion Equipment Software and an additional 3D code CPT® 76376 or CPT® 76377 should not be approved.

    ONC-19.1: Suspected Prostate Cancer

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ® Age 45-75 years and ONE of the following:
      ¡ PSA >3 ng/ml
      ¡ Very suspicious DRE
    ® Age >75 years and ONE of the following:
      ¡ PSA ≥4 ng/ml
      ¡ Very suspicious DRE
    ® At least one negative/non-diagnostic TRUS biopsy and EITHER of the following:
      ¡ Continued increase in PSA
      ¡ Abnormal DRE
    Any ONE of the following:
    ® Transrectal ultrasound (CPT® 76872)
    ® TRUS-guided biopsy (CPT® 76942)
    ® MRI Pelvis without and with contrast (CPT® 72197)
    ® MRI Pelvis without contrast (CPT® 72195)
    ® MRI/US fusion biopsy (CPT® 77021 and CPT® 76942)
    ® MRI guided biopsy (CPT® 77021)
      Due to a high rate of false negatives, MRI should not be used to make a decision not to biopsy.1
    ® PIRADS 4 or 5 lesion identified on recent diagnostic MRI Pelvis (CPT® 72195 or CPT® 72197) and planning for biopsy to be done by MRI/TRUS fusion technique ® 3D Rendering (CPT® 76377)
    ® CPT® 76376 should not be separately reimbursed
    Any of the following:
    ® Multifocal (3 or more lesions) high-grade prostatic intraepithelial neoplasia (PIN)
    ® Atypia on biopsy
    ® Extended pattern rebiopsy within 6 months by TRUS-guided biopsy (CPT® 76942)
    ® Focal PIN (1-2 lesions)One of the following may be approved:
    ® MRI Pelvis without contrast (CPT® 72195)
    ® MRI Pelvis without and with contrast (CPT® 72197)
    ® MRI/US fusion biopsy (CPT® 77021 and CPT® 76942)
    ® MRI guided biopsy (CPT® 77021)

    ONC-19.2: Prostate Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Pelvic imaging for any one of the following:
    ® Clinical stage T3 or T4 disease (palpable disease outside of the prostate capsule)
    ® Clinical stage T2b (tumor involving > 50% of one lobe) or stage T2c (tumor involving both lobes)
    ® Gleason score ≥ 7
    ® PSA > 10 ng/ml
    ® Nomogram predicts >10% probability of pelvic lymph node involvement
    One of the following can be approved:
    ® CT Pelvis with contrast (CPT® 72193)
    ® MRI Pelvis without and with contrast (CPT® 72197)
    Abdominal imaging for any of the following:
    ® PSA ≥ 20 ng/mL
    ® Gleason score ≥ 8
    ® Clinical stage ≥T3 or greater (palpable disease outside of the prostate capsule)
    ® At least 2 of the following are present:
      ¡ Clinical stage T2b (tumor involving > 50% of one lobe) or stage T2c (tumor involving both lobes)
      ¡ Gleason score ≥ 7
      ¡ PSA > 10 ng/mL
    One of the following can be approved:
    ® CT Abdomen with contrast (CPT® 74160)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) if being completed in the same imaging session as CT Pelvis
    Any of the following:
    ® Bone pain
    ® Gleason score ≥ 7
    ® PSA ≥ 20 ng/ml
    ® Clinical state ≥ T3 or greater (palpable disease outside of the prostate capsule)
    ® Clinical Stage T2b (tumor involving > 50 % of one lobe) or stage T2c (tumor involving both lobes) and with PSA > 10 ng/ml
    ® Bone scan (See ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    ® If neurological compromise, see:
      ONC-31.5: Bone (Including Vertebral) Metastases

    ONC-19.3: Prostate Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All members with one or more of the following:

    ® New finding on most recent CT or MRI that was inconclusive

    ® PSA rising on 2 consecutive measurements while on endocrine/hormonal therapy

    ® Clinical suspicion of recurrence or progression

    Any of the following can be approved:

    ® CT Abdomen/Pelvis with contrast (CPT® 74177)

    ® MRI Pelvis without contrast (CPT® 72195) or MRI Pelvis without and with contrast (CPT® 72197)

    Members with prior radical prostatectomy and any of the following:

    ® Palpable anastomotic recurrence

    ® PSA remains > 0.2 after at least 2 PSAs

    ® Initial undetectable PSA increasing on 2 consecutive PSAs

    Any of the following can be approved:

    ® CT Abdomen/Pelvis with contrast (CPT® 74177)


      ¡ MRI Pelvis without contrast (CPT® 72195) or MRI Pelvis without and with contrast (CPT® 72197) if CT findings are inconclusive

    ® Bone scan (See ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)

    ® Chest x-ray


      ¡ CT Chest with (CPT® 71260) or without contrast (CPT® 71250) for new findings on CXR, or new/worsening signs/symptoms.
    Members with prior Radiation Therapy and any of the following:

    ® Clinical suspicion of relapsed disease

    ® PSA increasing on at least 2 consecutive values above post-XRT baseline

    Any of the following can be approved:

    ® CT Abdomen/Pelvis with contrast (CPT® 74177)


      ¡ MRI Pelvis without contrast (CPT® 72195) or without and with contrast (CPT® 72197) if CT findings are inconclusive

    ® Bone scan (See ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)

    ® Chest x-ray

      ¡ CT Chest with (CPT® 71260) or without contrast (CPT® 71250) for new findings on CXR, or new/worsening signs/symptoms.
    ALL of the following:

    ® Prior treatment with prostatectomy and/or radiation therapy and
    ® Consecutive rise in PSA and
    ® PSA ≥2 ng/mL and
    ® CT scan and bone scan are negative for metastatic disease

    ONE of the following:

    ® 11C Choline PET/CT scan (CPT® 78815 or CPT® 78816)
    ® 18F-Fluciclovine PET/CT scan (CPT® 78815 or CPT® 78816)

    Hormone Refractory Prostate Cancer (HRPC):

    ® Receiving treatment with chemotherapy

    ® Receiving anti-androgen therapy

    ® CT Abdomen/Pelvis with contrast (CPT® 74177) and CT scan of any involved body part every 2 cycles (6 to 8 weeks)

    ® CT Abdomen/Pelvis with contrast (CPT® 74177) and CT scan of any involved body part every 3 months

    Prior to start of Xofigo (Radium-223) therapy® One time CT Chest/Abdomen/Pelvis with contrast (CPT® 71260 and CPT® 74177).
    All members with one or more of the following:

    ® Obvious progression by DRE with plans for prostatectomy or radiation therapy

    ® Repeat TRUS biopsy for rising PSA shows progression to a higher Gleason’s score with plans for prostatectomy or radiation therapy

    ® MRI Pelvis without contrast (CPT® 72195) or without and with contrast (CPT® 72197)

    ONC-19.4: Prostate Cancer – Follow-up On Active Surveillance

    For this condition imaging is medically necessary based on the following criteria:

    Active surveillance is being increasingly utilized in prostate cancer. This therapeutic option involves regimented monitoring of an individual with known diagnosis of low risk prostate cancer for disease progression, without specific anticancer treatment. While being treated with active surveillance, an individual is generally considered a potential candidate for curative intent treatment approaches in the event that disease progression occurs.

    It is important to distinguish active surveillance from watchful waiting (or observation), which is generally employed in members with limited life expectancy. Watchful waiting involves cessation of routine monitoring and treatment is initiated only if symptoms develop.

    Current active surveillance guidelines suggest the following protocol:

    PSA every 6 months

    Digital Rectal Exam (DRE) every 12 months

    Repeat TRUS-guided prostate biopsy every 12 months

    Repeat mpMRI (CPT® 72195 or CPT® 72197) no more often than every 12 months

    Routine use of MR/US fusion biopsy in active surveillance members is considered investigational at this time

    Due to a high rate of false negatives, MRI should not be used to make a decision not to biopsy.1
    Indication
    Imaging/Lab Study
    A member with ONE of the following:
    ® Progression is suspected based on DRE changes or rising PSA and a recent TRUS biopsy was negative
    ® Repeat TRUS biopsy shows progression to a higher Gleason score
    ® MRI pelvis without (CPT® 72195) or without and with contrast (CPT® 72197)

    ONC-19.5: Surveillance/Follow-up For Treated Prostate Cancer

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All Stages® PSA and DRE every 6 months, even in members with metastatic disease.
    ® Routine imaging is not indicated for members being monitored on or off therapy.


    References

    1. Mohler JL, Lee, RJ, Antonarakis ES, Armstrong AJ, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 - April 17, 2019. Prostate cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/prostate.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Prostate cancer V2.2019 – April 17, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – May 31, 2019 Prostate Cancer Early Detection available at: https://www.nccn.org/professionals/physician_gls/pdf/prostate_detection.pdf. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Prostate Cancer Early Detection V2.2019 – May 31, 2019 ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    3. ACR Appropriateness Criteria. Prostate cancer – pretreatment detection, surveillance, and staging. Rev. 2016.
    4. Sanda MG, Chen RC, Crispino T, et al. AUA/ASTRO/SUO guidelines for clinically localized prostate cancer. Linthicum, MD: American Urological Association; 2017.
    5. Lu-Yao GL, Albertsen PC, Moore DF, et al. Outcomes of localized prostate cancer following conservative management. JAMA. 2009;302(11):1202-1209. doi:10.1001/jama.2009.1348.
    6. Chen RC, Rumble RB, Loblaw DA, et al. Active surveillance for the management of localized prostate cancer (Cancer Care Ontario guideline): American Society of Clinical Oncology clinical practice guideline endorsement. J Clin Oncol. 2016;34(18):2182-2190. doi:10.1200/JCO.2015.65.7759.
    7. Liu D, Lehmann HP, Frick KD, Carter HB. Active surveillance versus surgery for low risk prostate cancer: a clinical decision analysis. J Urol. 2012;187(4):1241-1246. doi:10.1016/j.juro/2011.12.015.
    8. Klotz L, Zhang L, Lam A, Nam R, Mamedov A, Loblaw A. Clinical results of long-term follow-up of a large, active surveillance cohort with localized prostate cancer. J Clin Oncol. 2010;28(1):126-131. doi:10.1200/JCO.2009.24.2180.
    9. Blomqvist L, Carlsson S, Gjertsson P, et al. Limited evidence for the use of imaging to detect prostate cancer: a systematic review. Eur J Radiol. 2014;83(9):1601–1606. doi:10.1016.j.ejrad.2014.06.028.
    10. Schoots IG, Petrides N, Giganti F, et al. Magnetic resonance imaging in active surveillance of prostate cancer: a systematic review. Eur Urol. 2015;67(4):627-636. doi:10.1016/j.eururo.2014.10.050.
    11. Quentin M, Blondin D, Arsov C, et al. Prospective evaluation of magnetic resonance imaging guided in-bore prostate biopsy versus systematic transrectal ultrasound guided prostate biopsy in biopsy naïve men with elevated prostate specific antigen. J Urol. 2014;192(5):1374-1379. doi:10.1016/j.juro.2014.05.090.
    12. Klotz L, Vesprini D, Sethukavalan P, et al. Long-term follow-up of a large active surveillance cohort of patients with prostate cancer. J Clin Oncol. 2015;33(3):272-277. doi:10.1200/JCO.2014.55.1192.
    13. Cooperberg MR. Long-term active surveillance for prostate cancer: answers and questions. J Clin Oncol. 2015;33(3):238-240. doi:10.1200/JCO.2014.59.2329.
    14. Risko R, Merdan S, Womble PR, et al. Clinical predictors and recommendations for staging CT scan among men with prostate cancer. Urology. 2014;84(6):1329-1334. doi:10.1016.j.urology.2014.07.051.
    15.Heck MM, Souvatzoglou M, Retz M, et al. Prospective comparison of computed tomography, diffusion-weighted magnetic resonance imaging and [11C]choline positron emission tomography/computed tomography for preoperative lymph node staging in prostate cancer patients. Eur J Nucl Med Mol Imaging. 2014;41(4):694-701. doi:10.1007/s00259-013-2634-1.


    ONC-20: Testicular, Ovarian and Extragonadal Germ Cell Tumors


    ONC-20.0: Testicular, Ovarian and Extragonadal Germ Cell Tumors – General Considerations
    ONC-20.1: Testicular, Ovarian and Extragonadal Germ Cell Tumors – Initial Work-up/Staging
    ONC-20.2: Testicular, Ovarian and Extragonadal Germ Cell Tumors – Restaging/Recurrence
    ONC-20.3: Testicular, Ovarian and Extragonadal Germ Cell Tumors – Surveillance

    ONC-20.0: Testicular, Ovarian and Extragonadal Germ Cell Tumors – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    This section applies to primary germ cell tumors occurring outside the central nervous system in members age > 15 years at the time of initial diagnosis. Members age ≤ 15 years at diagnosis should be imaged according to pediatric guidelines in: Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-10: Pediatric Germ Cell Tumors

    These guidelines are for germ cell tumors of the testicle, ovary and extragonadal sites as well as malignant sex cord stromal tumors (granulosa cell and Sertoli-Leydig cell tumors).

    Requests for imaging must state the histologic type of the cancer being evaluated.

    Classified as pure seminomas (dysgerminomas, 40%) or Non-seminomatous germ cell tumors (NSGCT, 60%).

      ® Pure seminomas are defined as pure seminoma histology with a normal serum concentration of alpha fetoprotein (AFP). Seminomas with elevated AFP are by definition Mixed.
      ® Required for TNM staging are the tumor marker levels indicated by “S” (TNMS)
      ® Mixed tumors are treated as NSGCTs, as they tend to be more aggressive.
      ® The NSGCT histologies include:
        ¡ Yolk-Sac tumors
        ¡ Immature (malignant) teratomas
        ¡ Choriocarcinomas (< 1%)
        ¡ Embryonal cell carcinomas (15% to 20%)
        ¡ Endodermal Sinus Tumors (ovarian)
        ¡ Combinations of all of the above (Mixed)
    MRI in place of CT scans to reduce risk of secondary malignancy is not supported by the peer-reviewed literature. CT scans are indicated for surveillance and are the preferred modality of imaging to assess for recurrence.

    PET/CT Scan is not indicated for evaluation of non-seminomatous germ cell tumors

    ONC-20.1: Testicular, Ovarian and Extragonadal Germ Cell Tumors – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Orchiectomy/oophorectomy is both diagnostic and therapeuticAll members, following orchiectomy or oophorectomy:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    For any of the following:
    ® Non-seminoma histology
    ® Ovarian germ cell tumor
    ® Abdominal lymphadenopathy noted on CT scan
    ® Abnormal CXR or signs/symptoms suggestive of chest involvement
    ® CT Chest with contrast (CPT® 71260)
    Extragonadal Germ Cell Tumor® CT Chest with contrast (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177)
    ONC-20.2: Testicular, Ovarian and Extragonadal Germ Cell Tumors – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Treatment response for stage II-IV members with measurable disease on CT® CT with contrast of previously involved body areas every 2 cycles
    Seminoma with residual mass > 3 cm after completion of chemotherapy® PET/CT (CPT® 78815)
      ¡ PET imaging can be done as early as 6 weeks after completion of XRT if recent CT findings are inconclusive and PET findings will alter immediate care decision making
    End of therapy evaluation for NSGCT post chemotherapy or post retroperitoneal lymph node dissection (RPLND) ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    Recurrence suspected, including increased tumor markers® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® Ultrasound (CPT® 76856 or CPT® 76857) of the remaining gonad if applicable
    Unexplained pulmonary symptoms despite a negative CXR, or new findings on CXR® CT Chest with contrast (CPT® 71260)
    All others ® See Surveillance below

    ONC-20.3: Testicular, Ovarian and Extragonadal Germ Cell Tumors – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Stage I Seminoma treated with orchiectomy alone (no radiotherapy or chemotherapy, also called active surveillance)® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen with contrast (CPT® 74160) at 3, 6 and 12 months post-orchiectomy, then annually until year 5
    Stage I Seminoma treated with radiotherapy and/or chemotherapy® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen with contrast (CPT® 74160) annually for 3 years
    Stage IIA Seminomas treated with radiotherapy or chemotherapy® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen with contrast (CPT® 74160) once at 3 months then once at 6 to 12 months after completion of therapy, then annually until year 3
    Stage IIB, IIC, and III Seminomas treated with chemotherapyFor members with ≤ 3 cm residual mass:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen with contrast (CPT® 74160) every 4 months for 1 year, every 6 months for 1 year and then annually for 2 additional years

    For members with > 3 cm residual mass and negative PET scan:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen with contrast (CPT® 74160) at 6 and 12 months after completion of therapy, then annually until year 5

    For members with thoracic disease at diagnosis:
    ® CT Chest with contrast (CPT® 71260) every 2 months for 1 year, then every 3 months for 1 year, then annually until year 5

    Stage IA Non-Seminomatous germ cell tumors treated with orchiectomy alone (no radiotherapy or chemotherapy, also called active surveillance)® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen with contrast (CPT® 74160) at 6 and 12 months after orchiectomy, then annually until year 3
    Stage IB Non-Seminomatous germ cell tumors treated with orchiectomy alone (no radiotherapy or chemotherapy, also called active surveillance)® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen with contrast (CPT® 74160) every 4 months for 1 year, then every 6 months for 2 years, then annually until year 4
    Stage IA/IB Non-Seminomatous germ cell tumors treated with chemotherapy® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen with contrast (CPT® 74160) annually for 2 years
    Stage II-III Non-Seminomatous germ cell tumors with complete response to chemotherapy +/- post-chemotherapy RPLND® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen with contrast (CPT® 74160) once at 6, 12, 24 and 36 months after completion of therapy

    For members with thoracic disease at diagnosis:
    ® CT Chest with contrast (CPT® 71260) every 6 months for 2 years, then annually until year 4

    Stage IIA or IIB Non-Seminomatous germ cell tumors with post-primary RPLND complete resection +/- adjuvant chemotherapy® CT Abdomen/Pelvis with contrast (CPT® 74177) or CT Abdomen with contrast (CPT® 74160) once at 3 to 4 months after completion of therapy
    All ovarian germ cell tumors
    ® Dysgerminoma
    ® Embryonal tumor
    ® Endodermal sinus tumor
    ® Mature or immature teratoma
    ® Non-gestational choriocarcinoma
    ® No routine imaging unless elevated tumor markers or clinical signs/symptoms of recurrence
    Sex cord stromal tumors (male and female)® No routine advanced imaging indicated unless elevated tumor markers or clinical signs/symptoms of recurrence
    Extragonadal germ cell tumors® CT of the involved region every 3 months for one year and every 6 months for one year.

    1. Gilligan T, Beard C, Carneiro B, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2019 – October 22, 2018. Testicular cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/testicular.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Testicular cancer V 1.2019 –October 22, 2018. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Salani R, Backes FJ, Fung MF, et al. Post treatment surveillance and diagnosis of recurrence in women with gynecologic malignancies: Society of Gynecologic Oncologists recommendations. Am J Obstet Gynecol. 2011;204(6):466-478. doi:10.1016/j.ajog.2011.03.008.
    3. Gershenson DM. Management of ovarian germ cell tumors. J Clin Oncol. 2007;25(20):2938-2943. doi:10.1200/JCO.2007.10.8738.
    4. Colombo N, Parma G, Zanagnolo V, Insinga A. Management of ovarian stromal cell tumors. J Clin Oncol. 2007;25(20):2944-2951. doi:10.1200/JCO.2007.11.1005.
    5. Cadron I, Leunen K, Van Gorp T, Amant F, Neven P, Vergote I. Management of Borderline Ovarian Neoplasms. J Clin Oncol. 2007;25(20):2928-2937. doi:10.1200/JCO/2007.10.8076.
    6. del Carmen MG, Birrer M, Schorge JO. Carcinosarcoma of the ovary: a review of the literature. Gynecol Oncol. 2012;125(1):271-277. Doi:10.1016/j.ygyno.2011.12.418.
    7. Kollmannsberger C, Tandstad T, Bedard PL, et al. Patterns of relapse in patient with clinical stage I testicular cancer managed with active surveillance. J Clin Oncol. 2015;33(1):51-57. doi:10.1200/JCO.2014.56.2116.
    8. Oechsle K, Hartmann M, Brenner W, et al. [18F]Fluorodeoxyglucose positron emission tomography in nonseminomatous germ cell tumors after chemotherapy: the German multicenter positron emission tomography study group. J Clin Oncol. 2008;26(36):5930-5935. doi:10.1200/JCO.2008.17.1157.



    ONC-21: Ovarian Cancer

    ONC-21.0: Ovarian Cancer – General Considerations
    ONC-21.1: Screening for Ovarian Cancer
    ONC-21.2: Ovarian Cancer – Suspected/Diagnosis
    ONC-21.3: Ovarian Cancer – Initial Work-up/Staging
    ONC-21.4: Ovarian Cancer – Restaging/Recurrence
    ONC-21.5: Ovarian Cancer – Surveillance

    ONC-21.0: Ovarian Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Ovarian cancers include: epithelial ovarian cancers, ovarian cancers of low malignant potential and mixed Müllerian tumors, primary peritoneal and fallopian tube cancers.

    Germ cell tumors and sex cord stromal tumors (granulosa cell tumors), are imaged according to ONC-20: Testicular, Ovarian and Extragonadal Germ Cell Cancer.

    ONC-21.1: Screening for Ovarian Cancer

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging/Lab Study
    High Risk Factors:
    ® Family history of BRCA 1 or BRCA 2 mutations
    ® Family history of ovarian cancer
    ® Hereditary ovarian cancer syndrome that includes ovarian, breast, and/or endometrial and gastrointestinal cancers [Lynch II syndrome] in multiple members of two to four generations
    ® Low parity
    ® Decreased fertility
    ® Delayed childbearing
    ® Ovarian cancer screening is considered investigational and is not recommended.
    ® Genetic counseling is recommended for women with an increased-risk family history (USPSTF, 2015)
    Known BRCA-1 or BRCA-2 mutation® Transvaginal ultrasound (CPT® 76830), combined with CA-125 for ovarian cancer screening may be considered annually starting at age 30, until risk-reducing salpingo-oophorectomy is performed

    ONC-21.2: Ovarian Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See PV-5.3: Complex Adnexal Masses for imaging guidelines for evaluation of suspected ovarian malignancies
    Indication
    Imaging/Lab Study
    Elevated CA-125 and one of the following:
    ® Ultrasound is indeterminate or suspicious for ovarian malignancy
    ® Preoperatively prior to salpingo-oophorectomy
    ® Obstructive uropathy**
    ® Elevated LFTs
    ® CT Abdomen and Pelvis with contrast (CPT® 74177)
    ® **CT Abdomen/Pelvis without and with contrast (CPT® 74178) may be approved only for symptoms of obstructive uropathy
    ® MRI Pelvis without and with contrast (CPT 72197) may be considered in differentiating the origin of pelvic masses that are not of clear ovarian origin.

    ONC-21.3: Ovarian Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Clinical stage II disease or higher® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Chest with contrast (CPT® 71260) if abnormal signs/symptoms of pulmonary disease or abnormal chest x-ray
    Any of the following:
    ® Primary peritoneal disease with biopsy-proven malignancy consistent with ovarian carcinoma
    ® Elevated tumor markers with negative or inconclusive CT imaging
    ® PET/CT (CPT® 78815)

    ONC-21.4: Ovarian Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Completely resected or definitively treated with chemotherapy and normal(ized) tumor markers® No advanced imaging needed
    Any of the following:
    ® Unresected disease
    ® Unknown preoperative markers
    ® Difficult or abnormal examination
    ® Elevated LFTs
    ® Rising tumor markers (CA-125, inhibin)
    ® Signs or symptoms of recurrence
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Chest (CPT® 71260) for any of the following:
      ¡ Prior known thoracic disease
      ¡ New or worsening thoracic signs/symptoms or CXR findings
      ¡ Rising CA-125/inhibin levels
    ® CT negative or inconclusive and CA-125 continues to rise or elevated LFTs
    ® Conventional imaging failed to demonstrate tumor or if persistent radiographic mass with rising tumor markers
    ® PET/CT (CPT® 78815)

    ONC-21.5: Ovarian Cancer – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Stages I-III® No advanced imaging needed
    Locally advanced/Metastatic with measurable disease® See: ONC-1.2: Phases of Oncology Imaging and General Phase-Related Considerations


    References

    1. Morgan RJ, Armstrong DK, Plaxe SC, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2019 – March 8, 2019. Ovarian cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/ovarian.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Ovarian cancer V 1.2019 – March 8, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Daly MB, Pilarski R, Berry M, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 3.2019 – January 18, 2019. Genetic/Familial High-Risk Assessment: Breast and Ovarian, available at: https://www.nccn.org/professionals/physician_gls/pdf/genetics_screening.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Ovarian cancer V 3.2019 – January 18, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    3. Moyer VA, U.S. Preventive Services Task Force. Screening for ovarian cancer: U.S. Preventive Services Task Force reaffirmation recommendation statement. Ann Intern Med. 2012;157(12):900-904. doi:10.7326/0003-4819-157-11-201212040-00539.
    4. Cadron I, Leunen K, Van Gorp T, Amant F, Neven P, Vergote I. Management of borderline ovarian neoplasms. J Clin Oncol. 2007;25(20):2928-2937. doi:10.1200/JCO.2007.10.8076.
    5. ACR Appropriateness Criteria. Ovarian cancer screening. Rev. 2017.
    6. Rosenthal AN, Fraser LSM, Phipott S. Evidence of stage shift in women diagnosed with ovarian cancer during phase II of the United Kingdom familial ovarian cancer screening study. J Clin Oncol. 2017;35(13):13:1411-1420. doi:10.1200/JCO.2016.69.9330.
    7. Shinagare AB, O’Neill AC, Cheng S, et al. Advanced high-grade serous ovarian cancer: frequency and timing of thoracic metastases and the implications for chest imaging follow-up. Radiology. 2015;277(3):733-740. doi:10.1148/radiol.2015142467.
    8. Musto A, Grassetto G, Marzola MC, et al. Management of epithelial ovarian cancer from diagnosis to restaging: an overview of the role of imaging techniques with particular regard to the contribution of 18F-FDG PET/CT. Nucl Med Commun. 2014;35(6):588-597. doi:10.1097/MNM.0000000000000091.
    9. Fischerova D, Burgetova A. Imaging techniques for the evaluation of ovarian cancer. Best Pract Res Clin Obstet Gynaecol. 2014;28(5):697-720. doi:10.1016/j.bpobgyn.2014.04.006.


    ONC-22: Uterine Cancer

    ONC-22.0: Uterine Cancer – General Considerations
    ONC-22.1: Uterine Cancer – Suspected/Diagnosis
    ONC-22.2: Uterine Cancer – Initial Work-up
    ONC-22.3: Uterine Cancer – Restaging/Recurrence
    ONC-22.4: Uterine Cancer – Surveillance

    ONC-22.0: Uterine Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Gestational trophoblastic neoplasia (GTN) – see Adult Pelvis Imaging Policy (Policy #156 in the Radiology Section); PV-16: Molar Pregnancy and Gestational Trophoblastic Neoplasia (GTN)

    PET is not routinely indicated for initial diagnosis; staging or restaging of uterine cancer.

    Most common cell type is adenocarcinoma

    Imaging not routinely indicated for laparoscopic/minimally invasive surgery unless initial staging criteria are met. Pelvic and para-aortic lymphadenectomy can still be performed.

    ONC-22.1: Uterine Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:

    See Adult Pelvis Imaging Policy (Policy #156 in the Radiology Section); PV-2: Abnormal Uterine Bleeding for imaging guidelines for evaluation of suspected uterine malignancies

    ONC-22.2: Uterine Cancer – Initial Work-up

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Extra-uterine disease suspected and/or Grade 3 tumor.® MRI Pelvis without and with contrast (CPT® 72197) or CT Pelvis with contrast (CPT® 72193)
    Any of the following:
    ® Abdominal symptoms or abnormal examination findings
    ® Elevated LFTS
    ® Other imaging studies suggest liver involvement
    One of the following may be approved:
    ® CT Abdomen with contrast (CPT® 74160)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) if being completed in the same imaging session as CT Pelvis
    Any of the following histologies:
    ® Papillary serous
    ® Clear cell
    ® Carcinosarcoma
    ® Soft tissue sarcoma of the uterus
    ® Leiomyosarcoma
    ® Undifferentiated sarcoma
    ® Endometrial stromal sarcoma
    ® Poorly differentiated endometroid
    ® CT Chest (CPT® 71260) and Abdomen/Pelvis with contrast (CPT® 74177)
    Tumors detected incidentally or incompletely staged surgically AND any of the following high risk features:
    ® Myoinvasion > 50%
    ® Cervical stromal involvement
    ® Lymphovascular invasion
    ® Tumor > 2 cm
    ® CT Chest (CPT® 71260) and Abdomen/Pelvis with contrast (CPT® 74177)
    Considering fertility sparing surgery for well-differentiated Stage IA (grade 1) uterine cancer® Transvaginal ultrasound (CPT® 76830) and MRI pelvis without and with contrast (CPT® 72197)
    All other members® Routine advanced imaging not needed

    ONC-22.3: Uterine Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Unresectable, medically inoperable, or incompletely surgically staged membersOne of the following:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177) or
    ® MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast
    ® Unresected disease
    ® Difficult or abnormal examination
    ® Elevated LFTs or rising tumor markers
    ® Signs or symptoms of recurrence
    ® CT Chest (CPT® 71260) and Abdomen/Pelvis with contrast (CPT® 74177)
    Papillary serous, clear cell and carcinosarcoma of the uterusSee: Restaging/Recurrence section in:
    ONC-21.4: Ovarian Cancer
    Soft tissue sarcoma of the uterus, leiomyosarcoma, undifferentiated sarcoma, and endometrial stromal sarcomaSee: Restaging/Recurrence section in:
    ONC-12.3: Soft Tissue Sarcoma

    ONC-22.4: Uterine Cancer – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Papillary serous, clear cell and carcinosarcoma of the uterusSee: Surveillance section in:
    ONC-21.5: Ovarian Cancer
    Soft tissue sarcoma of the uterus, leiomyosarcoma, undifferentiated sarcoma, and endometrial stromal sarcomaSee: ONC-12.4: Soft Tissue Sarcoma Surveillance/Follow-up
    All others No advanced imaging needed


    References

    1. Koh WJ, Greer BE, Abu-Rustum NR, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 3.2019 – February 11, 2019. Uterine neoplasms, available at: https://www.nccn.org/professionals/physician_gls/pdf/uterine.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for uterine neoplasms V 3.2019 – February 11, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Fader AN, Boruta D, Olawaiye AB, Gehrig PA. Updates on uterine papillary serous carcinoma. Expert Rev Obstet Gynecol. 2009;4(6):647-657. doi:10.1586/eog.09.49.
    3. Boruta DM 2nd, Gehrig PA, Fader AN, Olawaiye AB. Management of women with uterine papillary serous cancer: A Society of Gynecologic Oncology (SGO) review. Gynecol Oncol. 2009;115(1):142-153. doi:10.1016/j.ygyno.2009.06.011.
    4. Olawaiye AB, Boruta DM 2nd. Management of women with clear cell endometrial cancer: a Society of Gynecologic Oncology (SGO) review. Gynecol Oncol. 2009;113(2):277-283. doi:10.1016/j.ygyno.2009.02.003.
    5. Salani R, Backes FJ, Fung MF et al. Post treatment surveillance and diagnosis of recurrence in women with gynecologic malignancies: Society of Gynecologic Oncologists recommendations. Am J Obstet Gynecol. 2011;204(6):466-478. doi:10.1016/j.ajog.2011.03.008.

    ONC-23: Cervical Cancer
    ONC-23.0: Cervical Cancer – General Considerations
    ONC-23.1: Cervical Cancer – Suspected/Diagnosis
    ONC-23.2: Cervical Cancer – Initial Work-up/Staging
    ONC-23.3: Cervical Cancer – Restaging/Recurrence
    ONC-23.4: Cervical Cancer – Surveillance

    ONC-23.0: Cervical Cancer – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Primary histology for cervical cancer is squamous cell. Other, less common histologies are adenosquamous and adenocarcinoma. If biopsy is consistent with one of these less common histologies, it is necessary to clarify that tumor is not of primary uterine origin.

    If the primary histology is uterine in origin, follow imaging recommendations for uterine cancer, see: ONC-22: Uterine Cancer.

    ONC-23.1: Cervical Cancer – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    AllBiopsy should be performed prior to imaging

    ONC-23.2: Cervical Cancer – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Stage IB1 or less:
    < 4 cm confined to the cervix
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® PET/CT (CPT® 78815) should be approved only to explain inconclusive findings on other advanced imaging studies. Requests will be forwarded to Medical Director.
    ® Chest x-ray
      ¡ CT Chest with contrast (CPT® 71260) is indicated if abnormal CXR or new/worsening thoracic signs/symptoms
    Stage IB2 or higher stagesAny of the following combination, not both:
    ® PET/CT (CPT® 78815 or CPT® 78816)
      or
    ® CT Chest with contrast (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177)
      ¡ MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast if CT contrast allergy or inconclusive CT findings
    Any size cervical cancer incidentally found in a hysterectomy specimen® CT Chest with Contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® MRI Abdomen (CPT® 74183) and Pelvis (CPT® 72197) without and with contrast if CT contrast allergy or inconclusive CT findings
    ® PET/CT (CPT® 78815 or CPT® 78816) if inconclusive conventional imaging

    ONC-23.3: Cervical Cancer – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ® Difficult or abnormal examination
    ® Elevated LFTs
    ® Signs or symptoms of recurrence
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast if CT contrast allergy or inconclusive CT findings
    ® PET/CT (CPT® 78815 or CPT® 78816) for inconclusive conventional imaging
    If primary therapy was surgery
      ® See Surveillance guidelines ONC-23.4: Cervical Cancer – Surveillance
    If primary therapy radiation therapy ± chemotherapy
    (no surgery)
    Any of the following, not both:
    ® PET/CT (CPT® 78815 or CPT® 78816) at least 12 weeks after completion of treatment
      OR
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177)
      ¡ MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast if CT contrast allergy or inconclusive CT findings
    Unresectable disease or metastatic disease on systemic treatmentEvery 2 cycles of treatment (commonly every 6 to 8 weeks):
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of other involved or symptomatic areas

    ONC-23.4: Cervical Cancer – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All members® No routine advanced imaging needed.

    References

    1. Koh WJ, Greer BE, Abu-Rustum NR, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 4.2019 – March 29, 2019. Cervical cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/cervical.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Cervical cancer V 4.2019 – March 29, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Salani R, Backes FJ, Fung MF et al. Post treatment surveillance and diagnosis of recurrence in women with gynecologic malignancies: Society of Gynecologic Oncologists recommendations. Am J Obstet Gynecol. 2011;204(6):466-478. doi:10.1016/j.ajog.2011.03.008.
    3. Zanagnolo V, Ming L, Gadducci A, et al. Surveillance procedures for patients with cervical carcinoma: a review of the literature. Int J Gynecol Cancer. 2009;19(3):194-201. doi:10.1111/IGC.0b013e3181a130f3.
    4. Elit L, Fyles AW, Devries MC, et al. Follow-up for women after treatment for cervical cancer: A systematic review. Gynecol Oncol. 2009;114(3):528-535. doi:10.1016/j.ygyno.2009.06.001.
    5. Schwarz JK, Siegel BA, Dehdashti F, Grigsby PW. Association of posttherapy positron emission tomography with tumor response and survival in cervical carcinoma. JAMA. 2007;298(19):2289-2295. doi:10.1001/jama.298.19.2289.
    6. Meads C, Davenport C, Malysiak S, et al. Evaluating PET-CT in the detection and management of recurrent cervical cancer: systematic reviews of diagnostic accuracy and subjective elicitation. BJOG. 2014;121(4):398-407. doi:10.1111/1471-0528.12488.
    7. Chu Y, Zheng A, Wang F, et al. Diagnostic value of 18F-FDG-PET or PET-CT in recurrent cervical cancer: a systematic review and meta-analysis. Nucl Med Commun. 2014; 35(2):144-150. doi:10.1097/MNM. 0000000000000026.



    ONC-24: Anal & Vaginal Cancer, Cancers of the External Genitalia

    ONC-24.0: Anal Carcinoma – General Considerations
    ONC-24.1: Anal Carcinoma – Suspected/Diagnosis
    ONC-24.2: Anal Carcinoma – Initial Work-up/Staging
    ONC-24.3: Anal Carcinoma – Restaging/Recurrence
    ONC-24.4: Anal Carcinoma – Surveillance
    ONC-24.5: Cancers of External Genitalia – General Considerations
    ONC-24.6: Cancers of External Genitalia – Initial Work-up/Staging
    ONC-24.7: Cancers of External Genitalia – Restaging/Recurrence
    ONC-24.8: Cancers of External Genitalia – Surveillance

    ONC-24.0: Anal Carcinoma – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Most are squamous cell carcinomas, although some transitional and cloacogenic carcinomas are seen.

    Tumors reported as adenocarcinomas of the anal canal are treated as rectal cancers

    Squamous cell carcinomas of the anal margin (such as Bowen’s disease and Paget’s disease), perianal, and perigenital areas are skin cancers. See ONC-5.6: Non-Melanoma Skin Cancers – Initial Work-up/Staging.

    ONC-24.1: Anal Carcinoma – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All® Advanced imaging prior to biopsy is not needed

    ONC-24.2: Anal Carcinoma – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All members® CT Chest with contrast (CPT® 71260)

    One of the following:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Abdomen with contrast (CPT® 74160) and MRI Pelvis without and with contrast (CPT® 72197)

    ® Stage II-III Squamous Cell Carcinoma of the Anal Canal and no evidence of metastatic disease by conventional imaging
    ® Inconclusive findings on conventional imaging
    ® PET/CT (CPT® 78815)

    ONC-24.3: Anal Carcinoma – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Stage I and II members® Routine advanced imaging not needed
    Stage III and IV members ® CT Abdomen/Pelvis with contrast (CPT® 74177) every 2 cycles (generally 6 to 8 weeks) during treatment and at the end of planned chemotherapy treatment
    ® CT Chest (CPT® 71260) if chest x-ray is abnormal or if symptoms of chest involvement
    ® Difficult or abnormal examination
    ® Elevated LFTs
    ® Signs or symptoms of recurrence
    ® Biopsy proven recurrence
    ® CT Chest (CPT® 71260) with contrast

    One of the following:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast

    Inconclusive findings on conventional imaging® PET/CT (CPT® 78815)

    ONC-24.4: Anal Carcinoma – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    For all stages® CT Chest (CPT® 71260) with contrast annually for 3 years
    ® ONE of the following annually for three years:
      ¡ CT Abdomen/Pelvis with contrast (CPT® 74177)
      ¡ CT Abdomen with contrast (CPT® 74160) and MRI Pelvis without and with contrast (CPT® 72197)

    ONC-24.5: Cancers of External Genitalia – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    These imaging guidelines are applicable for squamous cell carcinomas arising from the vulva, vagina, penis and scrotum


    ONC-24.6: Cancers of External Genitalia – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    For stage II or higherOne of the following:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Abdomen with contrast (CPT® 74160) and MRI Pelvis without and with contrast (CPT® 72197)
    ® CT Chest with contrast (CPT® 71260) is indicated only for:
      ¡ Signs/symptoms suggestive of chest involvement
      ¡ Abnormal findings on chest X-ray
    Inconclusive findings on conventional imaging® PET/CT (CPT® 78815)

    ONC-24.7: Cancers of External Genitalia – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ® Difficult or abnormal examination
    ® Elevated LFTs
    ® Signs or symptoms of recurrence
    ® Biopsy proven recurrence
    ® CT Chest (CPT® 71260) with contrast

    And any one of the following:
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® MRI Abdomen (CPT® 74183) and MRI Pelvis (CPT® 72197) without and with contrast

    Individuals receiving systemic treatment ® CT Abdomen/Pelvis with contrast (CPT® 74177) every 2 cycles (generally 6 to 8 weeks) during treatment and at the end of planned chemotherapy treatment
    ® CT Chest (CPT® 71260) if chest x-ray is abnormal or if symptoms of chest involvement
    Inconclusive findings on conventional imaging® PET/CT (CPT® 78815)

    ONC-24.8: Cancers of External Genitalia – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    ® All stages of vulvar and vaginal cancers® Routine advanced imaging is not indicated for asymptomatic surveillance
    ® Penile Cancer: stage I-IIIA® Routine advanced imaging is not indicated for asymptomatic surveillance
    ® Penile cancer: stages IIIB and higher® CT Abdomen/Pelvis with contrast (CPT® 74177) every 3 months for year 1, and then every 6 months for year 2, then no further routine advanced imaging indicated


    References

    1. Benson AB, Venook AP, Cederquist L, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2019 – March 15, 2019. Anal Carcinoma, available at: https://www.nccn.org/professionals/physician_gls/pdf/anal.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for anal carcinoma V1.2019 – March 15, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Flaig TW, Spiess PE, Agarwal N. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – May 13, 2019. Penile Cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/penile.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for penile cancer V2.2019 – May 13, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    3. Koh WJ, Greer BE, Abu-Rustum NR, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – December 17, 2018. Vulvar Cancer, available at: https://www.nccn.org/professionals/physician_gls/pdf/vulvar.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Anal carcinoma V2.2018 – December 17, 2018. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    4. Bhuva NJ, Glynne-Jones R, Sonoda L, Wong WL, Harrison MK. To PET or not to PET? That is the question. Staging in anal cancer. Ann Oncol. 2012;23(8):2078-2082. doi:10.1093/annonc/mdr599.
    5. Mistrangelo M, Pelosi E, Bellò M, et al. Role of positron emission tomography-computed tomography in the management of anal cancer. Int J Radiat Oncol Biol Phys. 2012;84(1):66-72. doi:10.1016/j.ijrobp.2011.10.048.
    6. Jones M, Hruby G, Solomon M, Rutherford N, Martin J. The role of FDG-PET in the initial staging and response assessment of anal cancer: a systematic review and meta-analysis. Ann Surg Oncol. 2015;22(11):3574-3581. doi:10.1245/s10434-015-4391-9.

    ONC-25: Multiple Myeloma and Plasmacytomas

    ONC-25.0: Multiple Myeloma and Plasmacytomas – General Considerations
    ONC-25.1: Multiple Myeloma and Plasmacytomas – Suspected/Diagnosis
    ONC-25.2: Multiple Myeloma and Plasmacytomas – Initial Work-up/Staging
    ONC-25.3: Multiple Myeloma and Plasmacytomas – Restaging/Recurrence
    ONC-25.4: Multiple Myeloma and Plasmacytomas – Surveillance

    ONC-25.0: Multiple Myeloma and Plasmacytomas – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Multiple myeloma (MM) is a neoplastic disorder characterized by the proliferation of a single clone of plasma cells derived from B cells which grows in the bone marrow and adjacent bone, producing skeletal destruction.

    Multiple myeloma group of disorders can be classified as below, which influence imaging modality of choice.
    Condition
    Monoclonal protein
    Bone marrow plasma cells
    CRAB criteria**
    Solitary Plasmacytoma (biopsy proven tumor containing plasma cells)
    < 3 gm/dL
    Absent
    Absent
    Monoclonal Gammopathy of Unknown Significance (MGUS)
    < 3 gm/dL
    < 10%
    Absent
    Smoldering Myeloma (SMM) (stage I MM or asymptomatic MM)
    ≥ 3 gm/dL
    10% - 60%
    Absent
    Multiple Myeloma (MM)
    ≥ 3 gm/dL
    ≥ 10%
    Present
    **CRAB criteria = hypercalcemia, renal insufficiency, anemia, lytic bony lesions

    Diagnosis and monitoring of response to therapy is primarily with laboratory studies that include urine and serum monoclonal protein levels, serum free light chain levels, LDH and beta-2 microglobulin. Routine advanced imaging to monitor response to treatment is not indicated.

    PET scans have not been shown to significantly alter therapeutic decisions and may only provide prognostic information.

    Rarely, (< 5%), an individual may have Nonsecretory Myeloma, which does not produce measurable M-protein. These members require imaging as primary method to monitor disease.

    For myeloma-like and lymphoma-like disease, see ONC-27: Non-Hodgkin Lymphomas.

    Other conditions that may present with Monoclonal Gammopathy include:

      ® POEMS syndrome: Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal protein and Skin Changes – these members may also have sclerotic bone lesions and Castleman’s disease
      ® Waldenstrom’s Macroglobulinemia: IgM monoclonal protein along with bone marrow infiltration of small lymphocytes. See ONC-27: Non-Hodgkin Lymphomas for imaging recommendations.
      ® Light chain Amyloidosis: light chain monoclonal protein in serum or urine with clonal plasma cells in bone marrow, systemic involvement of the kidneys, liver, heart, gastrointestinal tract or peripheral nerves due to amyloid deposition. See ONC-25: Multiple Myeloma and Plasmacytomas for imaging recommendations.

    ONC-25.1: Multiple Myeloma and Plasmacytomas – Suspected/Diagnosis

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    All ® X-ray skeletal series
    ONC-25.2: Multiple Myeloma and Plasmacytomas – Initial Work-up/Staging

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Any of the following:
    ® Abnormal skeletal survey
    ® Negative/equivocal skeletal survey with abnormal myeloma labs and/or symptoms of multiple myeloma
    One of the following:
    ® MRI Cervical (CPT® 72141), Thoracic (CPT® 72146), Lumbar spine (CPT® 72148), and Pelvis (CPT® 72195) without contrast
    ® MRI Cervical (CPT® 72156), Thoracic (CPT® 72157), Lumbar spine (CPT® 72158), and Pelvis (CPT® 72197) without and with contrast
    ® MRI Bone Marrow Blood Supply (CPT® 77084)
    ® CT contrast as requested of a specific area to determine radiotherapy or surgical candidacy, or for suspected extraosseous plasmacytoma
    For any of the following (after the tests listed above are completed):
    ® Determining if a plasmacytoma is truly solitary
    ® Suspected extraosseous plasmacytomas
    ® Suspected progression of MGUS or SMM to a more malignant form and CT/MRI imaging are negative
    ® Inconclusive conventional imaging
    ® PET/CT (CPT® 78815 or CPT® 78816)
    ONC-25.3: Multiple Myeloma and Plasmacytomas – Restaging/Recurrence

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Extra-osseous plasmacytoma response to initial therapy ® CT contrast as requested or MRI without contrast, or MRI without and with contrast of any previously involved area
    Laboratory tests fail to normalize with treatment® CT contrast as requested or MRI without contrast or MRI without and with contrast of symptomatic areas
    Known spine involvement with new neurological signs/symptoms or worsening pain® MRI Cervical (CPT® 72156), Thoracic (CPT® 72157), Lumbar spine (CPT® 72158) without and with contrast
    Any of the following:
    ® Suspected relapse/recurrence
    ® Suspected progression of MGUS or SMM to a more malignant form
    ® To determine therapy response with inconclusive labs
    One of the following:
    ® MRI without contrast, or MRI without and with contrast for any previously involved bony area or symptomatic area
    ® MRI Cervical (CPT® 72141), Thoracic (CPT® 72146), Lumbar spine (CPT® 72148), and Pelvis (CPT® 72195) without contrast
    ® MRI Cervical (CPT® 72156), Thoracic (CPT® 72157), Lumbar spine (CPT® 72158), and Pelvis (CPT® 72197) without and with contrast
    ® MRI Bone Marrow Blood Supply (CPT® 77084)
    Any of the following:
    ® Negative PET will allow change in management from active treatment to maintenance or surveillance.
    ® Determine additional therapies in refractory disease or non-secretory disease. These requests will be forwarded for Medical Director review.
    ® PET/CT (CPT® 78815 or CPT® 78816)
    Stem cell transplant recipientsOne of the following, once before transplant and once after transplant:
    ® MRI Bone Marrow Blood Supply (CPT® 77084)
    ® MRI Cervical (CPT® 72141), Thoracic (CPT® 72146), Lumbar spine (CPT® 72148), and Pelvis (CPT® 72195) without Contrast
    ® MRI Cervical (CPT® 72156), Thoracic (CPT® 72157), Lumbar spine (CPT® 72158), and Pelvis (CPT® 72197) without and with contrast
    ONC-25.4: Multiple Myeloma and Plasmacytomas – Surveillance

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Study
    Plasmacytomas® Skeletal survey annually
    All others, including Bone Marrow Transplant® Advanced imaging is not routinely indicated


    References

    1. Kumar SK, Callander NS, Alsina M, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 3.2019 – June 19, 2019. Myeloma, available at: https://www.nccn.org/professionals/physician_gls/pdf/myeloma.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Myeloma V3.2019 – June 19, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Kyle RA, Remstein ED, Therneau TM, et al. Clinical course and prognosis of smoldering (asymptomatic) multiple myeloma. N Engl J Med. 2007;356:2582-2590. doi:10.1056/NEJMoa070389.
    3. Dimopoulos M, Terpos E, Comenzo RL, et al. International myeloma working group consensus statement and guidelines regarding the current role of imaging techniques in the diagnosis and monitoring of multiple myeloma. Leukemia. 2009;23(9):1545-1556. doi:10.1038/leu.2009.89.
    4. ACR Committee on Drugs and Contrast Media. ACR Manual on Contrast Media, version 10.3. Reston, VA: American College of Radiology; 2018.
    5. Mulligan ME, Badros AZ. PET/CR and MR imaging in myeloma. Skeletal Radiol. 2007;36(1):5-16. doi:10.1007/s00256-006-0184-3.
    6. Dimopoulos MA, Hillengrass J, Usmani S, et al. Role of magnetic resonance imaging in the management of patients with multiple myeloma: a consensus statement. J Clin Oncol. 2015;33(6):657-664. doi:10.1200/JCO.2014.57.9961.
    7. Dimopoulos M, Terpos E, Comenzo RL, et al. International myeloma working group consensus statement and guidelines regarding the current role of imaging techniques in the diagnosis and monitoring of multiple myeloma. Leukemia. 2009;23(9):1545-1556. doi:10.1038.leu.2008.89.
    8. Dammacco F, Rubini G, Ferrari C, Vacca A, Racanelli V. 18F-FDG PET/CT: a review of diagnostic and prognostic features in multiple myeloma and related disorders. Clin Exp Med. 2015;15(1):1-18. doi:10.1007/s10238-014-0308-3.
    9. Ferraro R, Agarwal A, Martin-Macintosh EL, Peller PJ, Subramaniam RM. MR imaging and PET/CT in diagnosis and management of multiple myeloma. Radiographics. 2015;35(2):438-454. doi:10.1148/rg.352140112.
    10. Rajkumar SV, Kumar S. Multiple myeloma: diagnosis and treatment. Mayo Clin Proc. 2016;91(1):101-119. doi:10.1016/j.mayocp.2015.11.007.


    ONC-26: Leukemias, Myelodysplasia and Myeloproliferative Neoplasms

    ONC-26.1: Leukemias, Myelodysplasia and Myeloproliferative Neoplasms – General Considerations
    ONC-26.2: Acute Leukemias
    ONC-26.3: Chronic Myeloid Leukemias, Myelodysplastic Syndrome and Myeloproliferative Disorders
    ONC-26.4: Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL)

    ONC-26.1: Leukemias, Myelodysplasia and Myeloproliferative Neoplasms – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    PET imaging is considered investigational for all indications in acute lymphoblastic leukemia, acute myeloid leukemia, and chronic myeloid leukemia.

    Routine advanced imaging is not indicated in the evaluation and management of Hairy cell leukemia in the absence of specific localizing clinical symptoms.

    ONC-26.2: Acute Leukemias

    For this condition imaging is medically necessary based on the following criteria:

    Imaging indications for acute lymphoblastic leukemia in adult members are identical to those for pediatric members. See Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-3.2: Acute Lymphoblastic Leukemia (ALL) for imaging guidelines.

    Imaging indications for acute myeloid leukemia in adult members are identical to those for pediatric members. See Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-3.3: Acute Myeloid Leukemia (AML) for imaging guidelines.

    ONC-26.3: Chronic Myeloid Leukemias, Myelodysplastic Syndrome and Myeloproliferative Disorders

    For this condition imaging is medically necessary based on the following criteria:

    Routine advanced imaging is not indicated in the evaluation and management of chronic myeloid leukemias, myelodysplastic syndromes or myeloproliferative disorders in the absence of specific localizing clinical symptoms or clearance for hematopoietic stem cell transplantation.

    See ONC-29: Hematopoietic Stem Cell Transplantation for imaging guidelines related to transplant.

    For work-up of elevated blood counts, see ONC-30.3: Paraneoplastic Syndromes – General Considerations

    ONC-26.4: Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL)

    For this condition imaging is medically necessary based on the following criteria:

    PET imaging is not indicated in the evaluation of CLL/SLL with the exception of suspected Richter’s transformation (see Suspected transformation, below)

    CLL/SLL is monitored with serial laboratory studies. Routine advanced imaging is not indicated for monitoring treatment response or surveillance, except when initial studies reveal bulky disease involvement.

    Bulky disease is defined as lymph node mass > 5 cm or spleen > 6 cm below costal margin
    Indication
    Imaging Study
    Initial Staging/Diagnosis® Any or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    Treatment Response ® For members with bulky nodal disease at diagnosis, CT with contrast of previously involved area(s) every 2 cycles of therapy
    ® Routine imaging is not indicated for members without bulky nodal disease at diagnosis
    End of Therapy Evaluation® For members with bulky nodal disease at diagnosis, CT with contrast of previously involved area(s)
    Suspected progressionAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)
    Suspected transformation (Richter’s) from a low grade lymphoma to a more aggressive type based on one or more of the following:
    ® New B symptoms
    ® Rapidly growing lymph nodes
    ® Extranodal disease develops
    ® Significant recent rise in LDH above normal range
    ® PET/CT (CPT® 78815)
    Surveillance ® For members with bulky nodal disease at diagnosis, every 6 months for two years, then annually:
      ¡ CT Chest with contrast (CPT® 71260)
      ¡ CT Abdomen/Pelvis with contrast (CPT® 74177)
      ¡ CT with contrast of previously involved area(s)
    ® Routine imaging is not indicated for members without bulky nodal disease at diagnosis


    References

    1. Zelenetz AD, Gordon LI, Wierda WG, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 5.2019 – May 23, 2019. CLL/SLL, available at: https://www.nccn.org/professionals/physician_gls/pdf/cll.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for CLL/SLL V5.2019 – May 23, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Conte MJ, Bowen DA, Wiseman GA, et al. Use of positron emission tomography-computed tomography in the management of patients with chronic lymphocytic leukemia/small lymphocytic lymphoma. Leuk Lymphoma. 2014;55(9):2079-2084. doi:10.3109/10428194.2013.869801.
    3. Mauro FR, Chauvie S, Paoloni F, et al. Diagnostic and prognostic role of PET/CT in patients with chronic lymphocytic leukemia and progressive disease. Leukemia. 2015;29(6):1360-1365. doi:10.1038/leu.2015.21.
    4. Nabhan C, Rosen ST. Chronic lymphocytic leukemia: a clinical review. JAMA. 2014;312(21):2265-2276. doi:10.1001/jama.2014.14553.
    5. Patnaik MM, Tefferi A. Chronic myelomonocytic leukemia: focus on clinical practice. Mayo Clin Proc. 2016;91(2):259-272. doi:10.1016/j.mayocp.2015.11.011.


    ONC-27: Non-Hodgkin Lymphomas

    ONC-27.1: Non-Hodgkin Lymphomas – General Considerations
    ONC-27.2: Diffuse Large B Cell Lymphoma (DLBCL)
    ONC-27.3: Follicular Lymphoma
    ONC-27.4: Marginal Zone Lymphomas
    ONC-27.5: Mantle Cell Lymphoma
    ONC-27.6: Burkitt’s Lymphomas
    ONC-27.7: Lymphoblastic Lymphomas
    ONC-27.8: Cutaneous Lymphoma and T Cell Lymphomas

    ONC-27.1: Non-Hodgkin Lymphomas – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Lymphoma is often suspected when members have any of the following:

      ® Bulky lymphadenopathy (lymph node mass > 5 cm in size), hepatomegaly or splenomegaly
      ® The presence of systemic symptoms (fever, drenching night sweats or unintended weight loss of > 10%, called “B symptoms”)

    See ONC-31.11: Castleman’s Disease (Unicentric and Multicentric) for guidelines covering Castleman’s disease.

    See ONC-26.4: Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL) for guidelines covering Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL).
    Indication
    Imaging Study
    Evaluation of suspected or biopsy proven lymphoma® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
      ¡ MRI without and with contrast for individuals who cannot tolerate CT contrast due to allergy or impaired renal function
    Signs or symptoms of disease involving the neck® CT Neck with contrast (CPT® 70491)
    Signs or symptoms suggesting CNS involvement with lymphoma.® MRI Brain without and with contrast (CPT® 70553)

    ® See ONC-2.7: CNS Lymphoma (also known as Microglioma)

    Known or suspected bone involvement with lymphoma ® MRI without and with contrast of symptomatic or previously involved bony areas
      ¡ Bone scan is inferior to MRI for evaluation of known or suspected bone involvement with lymphoma
    Determine a more favorable site for biopsy when a relatively inaccessible site is contemplated® PET/CT (CPT® 78815 or CPT® 78816)
      ¡ PET/CT is not medically necessary for all other indications prior to histological confirmation of lymphoma

    ONC-27.2: Diffuse Large B Cell Lymphoma (DLBCL)

    For this condition imaging is medically necessary based on the following criteria:

    Grey zone lymphomas, primary mediastinal B cell lymphomas, grade 3 (high) follicular lymphoma and double-hit or triple-hit lymphomas should also be imaged according to these guidelines

    Post-transplant lymphoproliferative disorder (PTLD) or viral-associated lymphoproliferative disorder can rarely occur following solid organ or hematopoietic stem cell transplantation, or in primary immunodeficiency. These disorders may be treated similarly to high grade NHL when altering immunosuppressive regimens is unsuccessful, are highly FDG-avid, and should be imaged according to this section.

    PET/CT scan is not generally supported for interim restaging (monitoring response to treatment) due to increased false-positive results. Treatment intensification based on positive interim PET/CT scan does not improve outcomes. Any positive findings noted on an interim PET/CT scan should be biopsied before changing treatment.
    Indication
    Imaging Study
    Initial Staging/DiagnosisAny or all of the following may be approved:
    ® PET/CT (CPT® 78815 or CPT® 78816)
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    Treatment Response Any or all of the following may be approved every 2 cycles of therapy:
    ® CT with contrast of previously involved area(s)
    ® PET/CT is not indicated for monitoring response, but can be considered in rare circumstances when CT did not show disease (e.g bone). These cases should be forwarded for Medical Director review.
    End of Chemotherapy and/or Radiation Therapy EvaluationAny or all of the following may be approved:
    ® PET/CT (CPT® 78815 or CPT® 78816) may be approved at the end of chemo and again at the end of radiation
    ® CT with contrast of previously involved area(s)
    Suspected or Biopsy-Confirmed RecurrenceAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)
    ® PET/CT can be considered in rare circumstances (e.g. bone involvement). These cases should be forwarded for Medical Director review.
    CAR-T cell therapyOnce before treatment and once 30-60 days after completion of treatment:
    ® PET/CT (CPT® 78815 or CPT® 78816)
    Surveillance® Stage I and II:
      ¡ No routine advanced imaging indicated
    ® Stage III and IV:
      ¡ CT with contrast of previously involved area(s) every 6 months for two years, then no further routine advanced imaging
    ONC-27.3: Follicular Lymphoma

    For this condition imaging is medically necessary based on the following criteria:

    This section applies to follicular lymphomas with WHO grade of 1 (low) or 2 (intermediate). Grade 3 (high) follicular lymphomas should be imaged according to ONC-27.2: Diffuse Large B Cell Lymphoma (DLBCL)
    Indication
    Imaging Study
    Initial Staging/DiagnosisAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® PET/CT (CPT® 78815 or CPT® 78816) can be approved if XRT is being considered for stage I or II disease
    Treatment Response ® CT with contrast of previously involved area(s) every 2 cycles of therapy
    End of Therapy EvaluationOne of the following may be approved:
    ® CT with contrast of previously involved area(s)
    ® PET/CT (CPT® 78815 or CPT® 78816)
    Suspected RecurrenceAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)
    Suspected transformation (Richter’s) from a low grade lymphoma to a more aggressive type based on one or more of the following:
    ® New B symptoms
    ® Rapidly growing lymph nodes
    ® Extranodal disease develops
    ® Significant recent rise in LDH above normal range
    ® PET/CT (CPT® 78815)
    SurveillanceFor all stages, every 6 months for two years, then annually:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)
    ONC-27.4: Marginal Zone Lymphomas

    For this condition imaging is medically necessary based on the following criteria:

    MALT lymphomas in any location should also be imaged according to these guidelines

    Splenic Marginal Zone Lymphoma is diagnosed with splenomegaly, peripheral blood flow cytometry and bone marrow biopsy. Splenectomy is diagnostic and therapeutic. PET scan is not routinely indicated prior to splenectomy.
    Indication
    Imaging Study
    Initial Staging/DiagnosisAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)

    PET/CT (CPT® 78815 or CPT® 78816) can be approved if XRT is being considered for stage I or II disease

    Treatment Response ® CT with contrast of previously involved area(s) every 2 cycles of therapy
    End of Therapy EvaluationOne of the following may be approved:
    ® CT with contrast of previously involved area(s)
    ® PET/CT (CPT® 78815 or CPT® 78816)
    Suspected RecurrenceAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)
    ® PET/CT can be considered in rare circumstances (e.g. bone involvement). These cases should be forwarded for Medical Director review.
    SurveillanceFor all stages of nodal marginal zone lymphoma, the following is indicated every 6 months for two years, then annually:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)

    All stages of extranodal marginal zone lymphoma:
    ® No routine advanced imaging indicated

    ONC-27.5: Mantle Cell Lymphoma

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Initial Staging/DiagnosisAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)

    PET/CT (CPT® 78815 or CPT® 78816) can be approved if XRT is being considered for stage I or II disease

    Treatment Response ® CT with contrast of previously involved area(s) every 2 cycles of therapy
    ® PET/CT is not indicated for monitoring treatment response, but can be considered in rare circumstances when CT did not show disease (e.g. bone). These cases should be forwarded for Medical Director review
    End of Therapy EvaluationOne of the following may be approved:
    ® CT with contrast of previously involved area(s)
    ® PET/CT (CPT® 78815 or CPT® 78816)
    Suspected RecurrenceAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)
    ® PET/CT can be considered in rare circumstances (e.g. bone involvement). These cases should be forwarded for Medical Director review.
    SurveillanceAll Stages of Disease:
    ® No routine advanced imaging indicated
    ONC-27.6: Burkitt’s Lymphomas

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Initial Staging/DiagnosisAny or all of the following may be approved:
    ® PET/CT (CPT® 78815 or CPT® 78816)
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    Treatment Response ® CT with contrast of previously involved area(s) every 2 cycles of therapy
    ® PET/CT is not indicated for monitoring treatment response, but can be considered in rare circumstances when CT did not show disease (e.g. bone).These cases should be forwarded for Medical Director review.
    End of Therapy EvaluationAny or all of the following may be approved:
    ® PET/CT (CPT® 78815 or CPT® 78816) may be approved at the end of chemo and again at the end of radiation
    ® CT with contrast of previously involved area(s)
    Suspected RecurrenceAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)
    ® PET/CT can be considered in rare circumstances (e.g bone involvement). These cases should be forwarded for Medical Director review.
    SurveillanceAll Stages of Disease:
    ® No routine advanced imaging indicated

    ONC-27.7: Lymphoblastic Lymphomas

    For this condition imaging is medically necessary based on the following criteria:

    Members with lymphoblastic lymphoma (even those with bulky nodal disease) are treated using the leukemia treatment plan appropriate to the cell type (B or T cell). Imaging indications in adult members are identical to those for pediatric members. See Pediatric Oncology Imaging Policy (Policy #166 in the Radiology Section); PEDONC-3.2: Acute Lymphoblastic Leukemia (ALL) for imaging guidelines.

    ONC-27.8: Cutaneous Lymphoma and T Cell Lymphomas

    For this condition imaging is medically necessary based on the following criteria:

    Includes Primary Cutaneous B Cell Lymphomas, Peripheral T-Cell Lymphomas, Mycosis Fungoides/Sézary Syndrome, Anaplastic Large Cell Lymphoma, Primary Cutaneous CD30+T Cell Lymphoproliferative Disorders
    Indication
    Imaging Study
    Initial Staging/DiagnosisAny or all of the following may be approved:
    ® PET/CT (CPT® 78815 or CPT® 78816)
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    Treatment Response ® CT with contrast of previously involved area(s) every 2 cycles of therapy
    ® PET/CT is not indicated for monitoring treatment response, but can be considered in rare circumstances when CT did not show disease (e.g. bone). These cases should be forwarded for Medical Director review
    End of Therapy EvaluationAny or all of the following may be approved:
    ® PET/CT (CPT® 78815 or CPT® 78816) may be approved at the end of chemo and again at the end of radiation
    ® CT with contrast of previously involved area(s)
    Suspected RecurrenceAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)
    ® PET/CT can be considered in rare circumstances (e.g bone involvement). These cases should be forwarded for Medical Director review.
    Surveillance® Stage I and II:
      ¡ No routine advanced imaging indicated
    ® Stage III and IV:
      ¡ CT with contrast of previously involved area(s) every 6 months for two years, then no further routine advanced imaging


    References

    1. Zelenetz AD, Gordon LI, Wierda WG, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 4.2019 – June 18, 2019. B-cell lymphomas, available at: https://www.nccn.org/professionals/physician_gls/pdf/B-CELL.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for B-cell lymphomas V4.2019 – June 18, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Zelenetz AD, Gordon LI, Wierda WG, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019– December 17, 2018. T-cell lymphomas, available at: https://www.nccn.org/professionals/physician_gls/pdf/T-CELL.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for T-cell lymphomas V2.2019 – December 17, 2018. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    3. Cheson BD, Fisher RI, Barrington SF, et al. Recommendations for initial evaluation, staging, and response assessment for Hodgkin and Non-Hodgkin lymphoma: the Lugano classification. J Clin Oncol. 2014;32(27):3059-3067. doi:10.1200/JCO.2013.54.8800.
    4. Barrington SF, Mikhaeel NG, Kostakoglu L, et al. Role of imaging in the staging and response assessment of lymphoma: consensus of the International Conference on Malignant Lymphomas Imaging Working Group. J Clin Oncol. 2014;32(27):3048-3058. doi:10.1200/JCO.2013.53.5229.
    5. Thompson CA, Ghesquieres H, Maurer MJ, et al. Utility of routine post-therapy surveillance imaging in diffuse Large B-Cell Lymphoma. J Clin Oncol. 2014;32(31):3506-3512. doi:10.1200/JCO.2014.55.7561.
    6. El-Galaly TC, Jakobsen LH, Hutchings M, et al. Routine imaging for diffuse Large B-Cell Lymphoma in first complete remission does not improve post-treatment survival: a Danish-Swedish population-based study. J Clin Oncol. 2015;33(34):3993-3998. doi:10.1200/JCO.2015.62.0229.
    7. Huntington SF, Svoboda J, Doshi JA. Cost-effectiveness analysis of routine surveillance imaging of patients with diffuse Large B-Cell Lymphoma in first remission. J Clin Oncol. 2015;33(13):1467-1474. doi:10.1200/JCO.2014.58.5729.
    8. Mamot C, Klingbiel D, Hitz F, et al. Final results of a prospective evaluation of the predictive value of interim positron emission tomography in patients with diffuse large B-cell lymphoma treated with R-CHOP-14 (SAKK 38/07). J Clin Oncol. 2015;33(23):2523-2529. doi:10.1200/JCO.2014.58.9846.
    9. Mylam KJ, Nielsen AL, Pedersen LM, Hutchings M. Fluorine-18-fluorodeoxyglucose positron emission tomography in diffuse large B-cell lymphoma. PET Clin. 2014;9(4):443-455. doi:10.1016/j.cpet.2014.06.001.
    10. Avivi I, Zilberlicht A, Dann EJ, et al. Strikingly high false positivity of surveillance FDG-PET/CT scanning among patients with diffuse large cell lymphoma in the rituximab era. Am J Hematol. 2013;88(5):400-405. doi:10.1002/ajh.23423.
    11. Ulrich Dührsen, Stefan Müller, Bernd Hertenstein, et al. Positron emission tomography-guided therapy of aggressive non-Hodgkin lymphomas (PETAL): a multicenter, randomized phase III trial. J Clin Oncol. 2018;36(20):2024-2034. doi:10.1200/JCO.2017.76.8093.


    ONC-28: Hodgkin Lymphoma

    ONC-28.1: Hodgkin Lymphoma – General Considerations
    ONC-28.2: Classical Hodgkin Lymphoma
    ONC-28.3: Nodular Lymphocyte – Predominant Hodgkin Lymphoma

    ONC-28.1: Hodgkin Lymphoma – General Considerations

    For this condition imaging is medically necessary based on the following criteria:

    Lymphoma is often suspected when members have any of the following:

      ® Bulky lymphadenopathy (lymph node mass > 5 cm in size), hepatomegaly or splenomegaly
      ® The presence of systemic symptoms (fever, drenching night sweats or unintended weight loss of > 10%, called “B symptoms”)

    Members with AIDS-related lymphoma should be imaged according to the primary lymphoma histology

    The Deauville Criteria are internationally accepted criteria, which utilize a five-point scoring system for the FDG avidity of a Hodgkin's lymphoma or Non-Hodgkin's lymphoma tumor mass as seen on FDG PET.

      ® Score 1: No uptake above the background
      ® Score 2: Uptake ≤ mediastinum
      ® Score 3: Uptake > mediastinum but ≤ liver
      ® Score 4: Uptake moderately increased compared to the liver at any site
      ® Score 5: Uptake markedly increased compared to the liver at any site
      ® Score X: New areas of uptake unlikely to be related to lymphoma

      Indication
      Imaging Study
      Evaluation of suspected or biopsy proven lymphoma® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
        ¡ MRI without and with contrast for individuals who cannot tolerate CT contrast due to allergy or impaired renal function
      Signs or symptoms of disease involving the neck® CT Neck with contrast (CPT® 70491)
      Signs or symptoms suggesting CNS involvement with lymphoma.® MRI Brain without and with contrast (CPT® 70553)
      ® See ONC-2.7: CNS Lymphoma (also known as Microglioma)
      Known or suspected bone involvement with lymphoma ® MRI without and with contrast of symptomatic or previously involved bony areas
        ¡ Bone scan is inferior to MRI for evaluation of known or suspected bone involvement with lymphoma
      Determine a more favorable site for biopsy when a relatively inaccessible site is contemplated® PET/CT
        ¡ PET/CT is medically unnecessary for all other indications prior to histological confirmation of lymphoma

    ONC-28.2: Classical Hodgkin Lymphoma

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Initial Staging/DiagnosisAny or all of the following may be approved:
    ® PET/CT (CPT® 78815 or CPT® 78816)
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    Treatment Response One of the following, not both:
    ® PET/CT (CPT® 78815 or CPT® 78816) as frequently as every 2 cycles
    ® CT with contrast of previously involved areas as frequently as every 2 cycles
    End of Chemotherapy and/or Radiation Therapy EvaluationAny or all of the following may be approved:
    ® PET/CT (CPT® 78815 or CPT® 78816) may be approved at the end of chemo and again at the end of radiation (after 12 weeks of completion of radiation therapy)
    ® CT with contrast of previously involved area(s)
    Suspected RecurrenceAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)
    SurveillanceAny or all of the following may be approved at 6, 12, and 24 months after completion of therapy:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)

    In addition to the above studies:
    ® A single follow-up PET/CT may be approved

      > 12 weeks after radiation therapy if end of therapy PET/CT report documents Deauville 4 or 5 FDG avidity

    ONC-28.3: Nodular Lymphocyte – Predominant Hodgkin Lymphoma

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Initial Staging/DiagnosisAny or all of the following may be approved:
    ® PET/CT (CPT® 78815 or CPT® 78816)
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    Treatment Response One of the following, not both:
    ® PET/CT (CPT® 78815 or CPT® 78816) as frequently as every 2 cycles
    ® CT with contrast of previously involved areas as frequently as every 2 cycles
    End of Chemotherapy and/or Radiation Therapy EvaluationAny or all of the following may be approved:
    ® PET/CT (CPT® 78815 or CPT® 78816) may be approved at the end of chemo and again at the end of radiation (after 12 weeks of completion of radiation therapy)
    ® CT with contrast of previously involved area(s)
    Suspected RecurrenceAny or all of the following may be approved:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)
    Suspected transformation (Richter’s) from a low grade lymphoma to a more aggressive type based on one or more of the following:
    ® New B symptoms
    ® Rapidly growing lymph nodes
    ® Extranodal disease develops
    ® Significant recent rise in LDH above normal range
    ® PET/CT (CPT® 78815)
    SurveillanceAny or all of the following may be approved at 6, 12, and 24 months after completion of therapy:
    ® CT Chest with contrast (CPT® 71260)
    ® CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT with contrast of previously involved area(s)

    In addition to the above studies:
    ® A single follow-up PET/CT may be approved > 12 weeks after radiation therapy if end of therapy PET/CT report documents Deauville 4 or 5 FDG avidity


    References

    1. Hoppe RT, Advani RH, Ai WZ, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2019 – April 9, 2019. Hodgkin lymphoma, available at: https://www.nccn.org/professionals/physician_gls/pdf/hodgkins.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Hodgkins Lymphoma V1.2019 – April 9, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Cheson BD, Fisher RI, Barrington SF, et al. Recommendations for initial evaluation, staging, and response assessment for Hodgkin and Non-Hodgkin lymphoma: the Lugano classification. J Clin Oncol. 2014;32(27):3059-3067. doi:10.1200/JCO.2013.54.8800.
    3. Barrington SF, Mikhaeel NG, Kostakoglu L, et al. Role of imaging in the staging and response assessment of lymphoma: consensus of the International Conference on Malignant Lymphomas Imaging Working Group. J Clin Oncol. 2014;32(27):3048-3058. doi:10.1200/JCO.2013.53.5229.
    4. Pingali SR, Jewell SW, Havlat L, et al. Limited utility of routine surveillance imaging for classical Hodgkin lymphoma patients in first complete remission. Cancer. 2014;120:2122-2129.
    5. Ha CS, Hodgson DC, Advani R, et al. Follow-up of Hodgkin lymphoma. ACR Appropriateness Criteria® 2014;1-16.
    6. Picardi M, Pugliese N, Cirillo, M et al. Advanced-stage Hodgkin lymphoma: US/Chest radiography for detection of relapse in patients in first complete remission—a randomized trial of routine surveillance imaging procedures. Radiology. 2014;272:262-274.
    7. Gallamini A, and Kostakoglu L. Interim FDG-PET in Hodgkin lymphoma: a compass of a safe navigation in clinical trials? Blood. 2012;120(25):4913-4920.
    8. Biggi A, Gallamini A, Chauvie S, et al. International validation study for interim PET in ABVD-treated, advanced-stage Hodgkin lymphoma: interpretation criteria and concordance rate among reviewers. J Nucl Med. 2013; 54(5):683-690.
    9. Gallamini A, Barrington SF, Biggi, et al. The predictive role of interim positron emission tomography for Hodgkin lymphoma treatment outcome is confirmed using the interpretation criteria of the Deauville five-point scale. Haematologica. 2014; 99(6):1107-1113.
    10. El-Galaly TC, Mylam KJ, Brown P, et al. Positron emission tomography/computed tomography surveillance in patients with Hodgkin lymphoma in first remission has a low positive predictive value and high costs. Haematologica. 2012;97(6):931-936.


    ONC-29: Hematopoietic Stem Cell Transplantation

    ONC-29.1: General Considerations for Stem Cell Transplant

    ONC-29.1: General Considerations for Stem Cell Transplant

    For this condition imaging is medically necessary based on the following criteria:

    Terminology:
    A number of terms will be used to describe the transplant process of using chemotherapy ± radiation to ablate the recipient’s bone marrow stores, depending on the source of the hematopoietic stem cells and the indication, including bone marrow transplant (BMT), stem cell transplant (SCT), and hematopoietic stem cell transplant (HSCT).


    Transplant types:
    Allogeneic (“allo”): The donor and recipient are different people, and there are multiple types depending on the source of the stem cells and degree of match between donor and recipient. This is most commonly used in diseases originating in the hematopoietic system, such as leukemias and lymphomas, and bone marrow failure syndromes or metabolic disorders. Common types are:


      ® Matched sibling donor (MSD or MRD): Donor and recipient are full siblings and HLA-matched

      ® Matched unrelated donor (MUD): Donor and recipient are HLA matched but not related to each other

      ® Cord blood: Donor stem cells come from frozen umbilical cord blood not related to the recipient, sometimes from multiple different donors at once

      ® Haploidentical transplant (haplo): Donor is a half-HLA match to the recipient, usually a parent


    Autologous (“auto”): The donor and recipient are the same person, as with allogeneic there are multiple types of this transplant. Transplant is really a misnomer since the process involves delivery of high dose chemotherapy that is ablative to the bone marrow, requiring an infusion of stem cells to allow marrow recovery. As such, is more correctly called a rescue. Rescue is most commonly used for metastatic disease involving the hematopoietic system.

    Allo HSCT results in a much greater degree of immunosuppression than auto because of the need to allow the new immune system to chimerize with the recipient’s body. Immune reconstitution commonly takes more than a year for individuals who receive allo HSCT, and individuals remain at high risk for invasive infections until that has occurred.

    Pre-Transplant Imaging in HSCT:

    Pre-transplant imaging in HSCT generally takes place within 30 days of transplant, and involves a reassessment of the individual’s disease status as well as infectious disease clearance
    Indication
    Imaging
    Immediate pre-transplant period ® CT Sinuses, Neck, Chest, and/or Abdomen/Pelvis (contrast as requested)
    Assess renal function® Nuclear renal function study (CPT® 78708 or CPT® 78709)
    Assess cardiac function ® Echocardiogram (CPT® 93306, CPT® 93307 or CPT® 93308)
      ¡ MUGA scan (CPT® 78472) may be indicated in specific circumstances, see: Adult Cardiac Imaging Policy (Policy #149 in the Radiology Section); CD-12.1: Oncologic Indications for Cancer Therapeutics-Related Cardiac Dysfunction (CTRCD)
    Assess primary disease status® See disease-specific guideline

    Post-Transplant Imaging in HSCT:

    There are many common complications from HSCT, including infection, graft versus host disease, hepatic sinusoidal obstruction syndrome, restrictive lung disease, among others.

    Disease response generally takes place at ~Day +30 (autos and some allos) or ~Day +100 (allos) post-transplant.
    Indication
    Imaging
    Assess known or suspected HSCT complications® Site-specific imaging should generally be approved
    Assess primary disease status post-transplant® See disease-specific guidelines for surveillance imaging
    Individuals receiving tandem auto transplants (2-4 autos back-to-back, spaced 6 to 8 weeks apart)® Guideline recommended imaging can be repeated after each transplant
    Suspected Bronchiolitis obliterans with organizing pneumonia (BOOP) ® CT Chest without contrast (CPT® 71250)


    ONC-30: Medical Conditions with Cancer in the Differential Diagnosis

    ONC-30.1: Fever of Unknown Origin (FUO)
    ONC-30.2: Unexplained Weight Loss
    ONC-30.3: Paraneoplastic Syndromes

    ONC-30.1: Fever of Unknown Origin (FUO)

    For this condition imaging is medically necessary based on the following criteria:

    FUO is defined as a persistent fever ≥ 101oF and ≥ 3 weeks with unidentified cause.

    While fever is a classic “B” symptom of advanced lymphoma, a cancer- related fever presenting in isolation without any other signs or symptoms of neoplastic disease is rare.
    Indication
    Imaging Study
    In addition to physical examination, based on suspected location, one can consider:® Chest x-ray
    ® Echocardiogram (CPT® 93306)
    ® Abdominal ultrasound (CPT® 76700)
    ® MRI Brain without and with contrast (CPT® 70553)
    Above studies (including PE/ENT exam, pelvic exam, and DRE with laboratory studies) have failed to demonstrate site of infection ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® Radiopharmaceutical localization of tumor or distribution of radiopharmaceutical agent(s): CPT® 78800, 78801, or 78802, CPT® 78804, CPT® 78803 (SPECT), or CPT® 78830, 78831, or 78832 (SPECT/CT)
    “B” symptoms ® See ONC-27: Non Hodgkin Lymphomas
    Any CNS sign/symptom accompanied by fever ® MRI Brain without and with contrast (CPT® 70553)
    All members® PET is not indicated in the work-up of members with FUO
    ONC-30.2: Unexplained Weight Loss

    For this condition imaging is medically necessary based on the following criteria:

    Unintentional weight loss is defined as loss of ≥ 10 lbs. or ≥5% of body weight over 6 months or less, without an identifiable reason.
    Potential causes of weight loss and initial evaluation
    Dysphagia and early satietyEndoscopy and/or barium swallow
    Panhypopituitarism or hyperthyroidismEndocrine evaluation, including tests for TSH and ACTH
    HypogonadismEndocrine evaluations for gonadal function
    Occult GI bleedingSerial tests for heme in stools
    Depression and early dementiaDetailed neurological examination

    Advanced imaging, as follows, may be indicated if the initial evaluations did not identify the cause of weight loss.
    Indication
    Imaging Study
    Any abnormality of pituitary hormones® MRI of the sella turcica without and with contrast (CPT® 70553)
    Elevated thyroglobulin level® Nuclear thyroid scan, or
    ® Thyroid ultrasound (CPT® 76536)
    Rule out renal, hepatic pathologies® Abdominal ultrasound (CPT® 76700)
    Rule out cardiac pathologies® Echocardiogram (CPT® 93306)
    For non-smokers® Chest x-ray should be performed initially
    For current or former smokers® CT Chest with contrast (CPT® 71260)
    If all of the above do not identify cause of weight loss ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    PET is not appropriate in the work-up of individuals with unexplained weight loss.
    ONC-30.3: Paraneoplastic Syndromes

    For this condition imaging is medically necessary based on the following criteria:

    General Considerations

    Paraneoplastic syndromes are metabolic and neuromuscular disturbances. These syndromes are not directly related to a tumor or to metastatic disease. There may be a lead time between initial finding of a possible paraneoplastic syndrome and appearance of the cancer with imaging. Limited studies suggest annual imaging for 2 years after diagnosis of possible paraneoplastic syndrome may detect cancer, however benefit after 2 years is not well documented.

    The following are the most common symptoms of paraneoplastic syndromes known to arise from various malignancies:

      ® Hypertrophic Pulmonary Osteoarthropathy: Often presents as a constellation of rheumatoid-like polyarthritis, periostitis of long bones, and clubbing of fingers and toes
      ® Amyloidosis
      ® Hypercalcemia
      ® Hypophosphatemia
      ® Cushing’s Syndrome
      ® Somatostatinoma syndrome (vomiting, abdominal pain, diarrhea, cholelithiasis)
      ® Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
      ® Polymyositis/dermatomyositis
      ® Opsoclonus
      ® Paraneoplastic sensory neuropathy
      ® Subacute cerebellar degeneration
      ® Eaton-Lambert syndrome (a myasthenia-like syndrome)
      ® Second event of unprovoked thrombosis
      ® Disseminated Intravascular Coagulation
      ® Migratory thrombophlebitis
      ® Polycythemia
      ® Chronic leukocytosis and/or thrombocytosis
      ® Elevated tumor markers

    See also: Adult Peripheral Nerve Disorders Imaging Policy (Policy #157 in the Radiology Section); PND-6: Muscle Disorders in the Peripheral Nerve Disorders Guidelines

    See also: ONC-25: Multiple Myeloma and Plasmacytomas for evaluation of possible multiple myeloma.
    Indication
    Imaging Study
    Initial evaluation
      ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    Any of the following:
      ® Abnormality on conventional imaging difficult to biopsy
      ® Inconclusive conventional imaging
      ® Documented paraneoplastic antibody and conventional imaging fails to demonstrate primary site
      ® PET/CT (CPT® 78815 or CPT® 78816)
    Subsequent evaluation for known paraneoplastic syndrome
      ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast may be repeated every 6 months for 2 years after initial imaging for Lambert-Eaton Myasthenia syndrome

      ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast may be repeated every 6 months for 4 years for all other paraneoplastic syndromes
    First episode of unprovoked DVT/VTE
      ® Imaging to evaluate for malignancy is not indicated
    Second unprovoked DVT/PE
      ® Imaging may be considered in the setting of a negative work-up for inherited thrombophilia and antiphospholipid syndrome
    In addition thyroid US is recommended for elevated CEA, and upper/lower endoscopy is recommended for elevated CEA or CA 19-9.

    References

    1. Carrier M, Lazo-Langner A, Shivakumar S, et al. Screening for occult cancer in unprovoked venous thromboembolism. N Engl J Med. 2015 June;373:697-704. doi:10.1056/NEJMoa1506623.
    2. Sioka C, Fotopoulos A, Kyritsis AP. Paraneoplastic neurological syndromes and the role of PET imaging. Oncology. 2010;78(2):150–156. doi:10.1159/000312657.
    3. Schramm N, Rominger A, Schmidt C, et al. Detection of underlying malignancy in patients with paraneoplastic neurological syndromes: comparison of 18F-FDG PET/CT and contrast-enhanced CT. Eur J Nucl Med Mol Imaging. 2013;40(7):1014-1024. doi:10.1007/s00259-013-2372-4.
    4. Qiu L, Chen Y. The role of 18F-FDG PET or PET/CT in the detection of fever of unknown origin. Eur J Radiol. 2012;81(11):3524-3529. doi:10.1016/j.ejrad.2012.05.025.
    5. Pelosof LC, Gerber DE. Paraneoplastic syndromes: an approach to diagnosis and treatment. Mayo Clin Proc. 2010;85(9):838-854. doi:10.4065/mcp.2010.0099.
    6. Wong CJ. Involuntary weight loss. Med Clin North Am. 2014;98(3):625-43. doi:10.1016/j.mcna.2014.01.012.
    7. Titulaer MJ, Soffieti R, Dalmau J, et al. Screening of tumours in paraneoplastic syndromes: report of an EFNS task force. Eur J Neurol. 2011;18(1):19–e3. doi:10.1111/j.1468-1331.2010.03220.x.
    8. Lancaster E. Paraneoplastic disorders. Continuum (Minneap Minn). 2017;23(6, Neuro-oncology):1653-1679. doi:10.1212/CON.0000000000000542.

    ONC-31: Metastatic Cancer, Carcinoma of Unknown Primary Site, and Other Types of Cancer


    ONC-31.1: Lung Metastases
    ONC-31.2: Liver Metastases
    ONC-31.3: Brain Metastases
    ONC-31.4: Adrenal Gland Metastases
    ONC-31.5: Bone (including Vertebral) Metastases
    ONC-31.6: Spinal Cord Compression
    ONC-31.7: Carcinoma of Unknown Primary Site
    ONC-31.8: Extrathoracic Small Cell and Large Cell Neuroendocrine Tumors
    ONC-31.9: Primary Peritoneal Mesothelioma
    ONC-31.10: Kaposi’s Sarcoma
    ONC-31.11: Castleman’s Disease (Unicentric and Multicentric)

    Guideline sections ONC-31.1: Lung Metastases through ONC-31.5: Bone (including Vertebral) Metastases should only be used for members with metastatic cancer in the following circumstances:

      ® The primary diagnosis section does not address a particular metastatic site that is addressed in these sections
      ® The cancer type is rare and does not have its own diagnosis-specific imaging guidelines

    ONC-31.1: Lung Metastases

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    New or worsening signs or symptoms suggestive of metastatic lung involvement or new or worsening chest x-ray abnormality® CT Chest with contrast (CPT® 71260)
    ® CT Chest without contrast (CPT® 71250) can be approved if there is a contraindication to CT contrast or only parenchymal lesions are being evaluated
    Chest wall or brachial plexus involvement® MRI Chest without and with contrast (CPT® 71552)
    One of the following and no diagnosis-specific guideline regarding PET imaging:
    ® Lung nodule(s) ≥ 8 mm
    ® Confirm solitary metastasis amenable to resection on conventional imaging
    ® PET/CT (CPT® 78815)
    ® When primary cancer known, PET request should be reviewed by primary cancer guideline
    Previous or current malignancy and pulmonary nodule(s) that would reasonably metastasize to the lungs® CT Chest with contrast (CPT® 71260) at 3, 6, 12 and 24 months from the first study
    ONC-31.2: Liver Metastases

    For this condition imaging is medically necessary based on the following criteria:

    Ablation of liver metastases or primary HCC may be performed utilizing chemical, chemotherapeutic, radiofrequency, or radioactive isotope methods. Regardless of the modality of ablation, PET is not indicated for assessing response to this mode of therapy.
    Indication
    Imaging Study
    New or worsening signs or symptoms suggestive of metastatic liver involvement or new elevation in LFTs.® CT Abdomen with (CPT® 74160) or without and with contrast (CPT® 74170)
    Any of the following:
    ® Considering limited resection
    ® Inconclusive CT findings
    ® MRI Abdomen without and with contrast (CPT® 74183)
    One of the following and no diagnosis-specific guideline regarding PET imaging:
    ® Confirm solitary metastasis amenable to resection on conventional imaging
    ® LFT’s and/or tumor markers continue to rise and CT and MRI are negative
    ® PET/CT (CPT® 78815)
      ¡ When primary cancer known, PET request should be reviewed by primary cancer guideline
    Monitoring of liver metastases that have been surgically resected® Review according to primary cancer guideline
    Evaluation for hepatic artery chemotherapy infusion or chemoembolization with radioactive spheres (TheraSphere or SIR Spheres) for liver metastases or primary liver tumors:® CTA Abdomen (CPT® 74175) can be approved immediately prior to embolization

    One of the following studies may be approved PRE-treatment based upon provider preference:
    ® Liver Imaging Planar (CPT® 78201) or Liver Imaging SPECT (CPT® 78205)
    ® Radiopharmaceutical Localization Limited Area (CPT® 78800)
    ® Liver Imaging SPECT (CPT® 78803)

    One of the following studies may be approved POST-treatment based upon provider preference:
    ® Liver Planar Imaging (CPT® 78201) or Liver Imaging SPECT (CPT® 78205)
    ® Radiopharmaceutical Localization Limited Area (CPT® 78800)
    ® Liver Imaging SPECT (CPT® 77803)

    Please note: liver-lung shunt calculation is included in the pre-treatment Liver Scan and does not require additional Lung Perfusion Scan

    Monitoring of ablated liver metastases or primary tumorsOne of the following, immediately prior to ablation, 1 month post-ablation, then every 3 months for 2 years, and then annually
    ® CT Abdomen without and with contrast (CPT® 74170)
    ® MRI Abdomen without and with contrast (CPT® 74183)
    ONC-31.3: Brain Metastases

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Individual with cancer and signs or symptoms of CNS disease or known brain metastasis with new signs or symptoms.® MRI Brain without and with contrast (CPT® 70553)
    Assess candidacy for stereotactic radiosurgical approach for brain metastases® MRI Brain without and with contrast (CPT® 70553) using thin slice cuts if not already done within 30 days
    ® If thin slice MRI done within 30 days and MRI needed for SRS treatment planning, planning code CPT® 76498 can be approved.
    Monitoring of brain metastases treated with surgery or radiation therapy Post-treatment, then every 3 months for 1 year and every 6 months thereafter:
    ® MRI Brain without and with contrast (CPT® 70553)

    ***Individuals treated with stereotactic radiosurgery alone may have MRI Brain without and with contrast (CPT® 70553) every 2 months for the first year and then every 3 months thereafter

    PET Metabolic Brain (CPT® 78608) and MR Spectroscopy (CPT® 76390) are considered investigational for evaluation of metastatic brain cancer

    Any of the following:
    ® Solitary brain metastasis suspected in member with prior diagnosis of cancer and no diagnosis-specific guideline regarding PET imaging
    ® Brain metastases and no known primary tumor
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    ® Mammography for female members
    ® PET/CT (CPT® 78815 or CPT® 78816) is indicated for any of the following:
      ¡ Inconclusive conventional imaging
      ¡ Confirm either stable systemic disease or absence of other metastatic disease
      ¡ When primary cancer known, PET request should be reviewed by primary cancer guideline
    Primary brain tumorsSee: ONC-2: Primary Central Nervous System Tumors
    ONC-31.4: Adrenal Gland Metastases

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Differentiate benign adrenal adenoma from metastatic disease® See Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-16: Adrenal Cortical Lesions
    Any of the following in an individual with known cancer:
    ® Adrenal mass ≥ 4 cm
    ® Enlarging solitary adrenal mass
    ® Inconclusive findings on recent CT scan
    One of the following:
    ® CT-directed needle biopsy (CPT® 77012)
    ® MRI Abdomen without (CPT® 74181) or without and with contrast (CPT® 74183)
    ® PET/CT (CPT® 78815)
      ¡ When primary cancer is known, PET request should be reviewed by primary cancer guideline
    ® See also Adult Abdomen Imaging Policy (Policy #148 in the Radiology Section); AB-16: Adrenal Cortical Lesions
    ONC-31.5: Bone (including Vertebral) Metastases

    For this condition imaging is medically necessary based on the following criteria:

    Members with Stage IV cancer with new onset back pain can forgo a bone scan (and plain films) in lieu of an MRI with and without contrast of the spine.
    Indication
    Imaging Study
    Any of the following in a member with a current or prior malignancy:
    ® Bone pain
    ® Rising tumor markers
    ® Elevated alkaline phosphatase
    ® Bone scan (see ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology) supplemented by plain x-rays is the initial diagnostic imaging study of choice
    Any of the following:
    ® Any member with stage IV cancer with new onset back pain
    ® Bone scan is not feasible or readily available
    ® Continued suspicion despite inconclusive or negative bone scan or other imaging modalities
    ® Neurological compromise
    ® Soft tissue component suggested on other imaging modalities or physical exam
    ® Differentiate neoplastic disease from Paget’s disease of bone
    ® Suspected leptomeningeal involvement
    Any of the following may be approved:
    ® MRI Cervical (CPT® 72156), Thoracic (CPT® 72157), and Lumbar spine (CPT® 72158) without and with contrast
    ® CT Cervical (CPT® 72127), Thoracic (CPT® 72130), and Lumbar spine (CPT® 72133) without and with contrast can be approved if MRI is contraindicated or not readily available
    ® CT without contrast can be approved if there is a contraindication to CT contrast
    Monitoring untreated spinal metastases® MRI without and with contrast or CT without and with contrast of the involved spinal level every 3 months for 1 year.

    **Imaging beyond 1 year is based on any new clinical signs/symptoms

    Monitoring metastases within the spine treated with surgery and/or radiation therapy® MRI without and with contrast or CT without and with contrast of the involved spinal level once within 3 months post treatment and then every 3 months for 1 year.

    **Imaging beyond 1 year is based on any new clinical signs/symptoms

    Leptomeningeal involvement with cancer On active treatment:
    ® MRI Brain without and with contrast (CPT® 70553)
    ® MRI Cervical (CPT® 72156), Thoracic (CPT® 72157), and Lumbar spine (CPT® 72158) without and with contrast every 2 cycles

    Once treatment completed:
    ® Routine advanced imaging not indicated for surveillance in asymptomatic individuals

    Bone pain when both bone scan and either CT or MRI are inconclusive® 18F-FDG-PET/CT (CPT® 78815 or CPT® 78816) on a case-by-case basis
    NOTE: 18F-NaF PET imaging (sodium fluoride, or “PET bone scan”) is investigational.
    See: ONC-1.4: PET Imaging in Oncology
    Suspected metastatic bone disease and negative work-up for myeloma® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) with contrast
    No prior cancer history with suspected pathologic fracture on plain x-ray® See ONC-31.7: Carcinoma of Unknown Primary Site
    Signs/symptoms concerning for spinal cord compression® See ONC-31.6: Spinal Cord Compression
    ONC-31.6: Spinal Cord Compression

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Any of the following in a current or former cancer member:
    ® Any member with stage IV cancer with new onset back pain
    ® New back pain persisting over two weeks
    ® Back pain that is rapidly progressive or refractory to aggressive pain management
    ® Signs or symptoms of neurological compromise at the spinal cord level
    ® Unexpected, sudden loss of bowel or bladder control
    ® Sudden loss of ability to ambulate
    ® Complete loss of pinprick sensation corresponding to a specific vertebral level
    ® Loss of pain at a site that had previously been refractory to pain management
    Any or all of the following may be approved:
    ® MRI Cervical (CPT® 72156), Thoracic (CPT® 72157), and Lumbar spine (CPT® 72158) without and with contrast
    ® Post myelogram CT of the Cervical (CPT® 72126), Thoracic (CPT® 72129), and Lumbar spine (CPT® 72132)
    Any current or former cancer member with radicular symptoms suggestive of nerve root involvement but not consistent with cord compression and one of the following:
    ® Unilateral weakness
    ® Unilateral change of reflexes
    ® Pain unrelieved by change in position
    ® Age > 70 years
    ® Unintentional weight loss
    ® Night pain
    One of the following:
    ® MRI without and with contrast of involved spinal level
    ® MRI without contrast of the involved spinal level
    ® CT without contrast of the involved spinal level if MRI contraindicated
    ONC-31.7: Carcinoma of Unknown Primary Site

    For this condition imaging is medically necessary based on the following criteria:

    General Considerations

    Defined as carcinoma found in a lymph node or in an organ known not to be the primary for that cell type (e.g., adenocarcinoma arising in the brain or in a neck lymph node).

    This guideline also applies to a pathologic fracture that is clearly due to metastatic neoplastic disease in a member without a previous cancer history.

    Detailed history and physical examination including pelvic and rectal exams and laboratory tests to be performed before advanced imaging.

    Members presenting with a thoracic squamous cell carcinoma described as metastatic appearing on chest imaging, or in lymph nodes above the clavicle, should undergo a detailed head and neck examination by a clinician skilled in laryngeal and pharyngeal examinations, especially in smokers.

    Members with suspected unknown primary carcinomas based on only suspicious lytic bone lesions should be considered for serum protein electrophoresis (SPEP); urine protein electrophoresis (UPEP) and serum free light chains prior to consideration of extensive imaging
    Indication
    Imaging Study
    Carcinoma found in a lymph node or in an organ known not to be primary
      ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177)
      ® CT Neck with contrast (CPT® 70491) if cervical or supraclavicular involvement
      ® CT with contrast or MRI without and with contrast of any other symptomatic site
      ® For female members:
      ¡ Diagnostic (not screening) mammogram and full pelvic exam
      ¡ MRI Bilateral Breasts (CPT® 77049) if pathology consistent with breast primary and mammogram is inconclusive
    Sebaceous carcinoma of the skin (can be associated with underlying primary malignancy) ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® CT Neck with contrast (CPT® 70491) if cervical or supraclavicular involvement
    ® CT with contrast or MRI without and with contrast of any other symptomatic site
    Axillary adenocarcinoma ® Diagnostic (not screening) mammogram and full pelvic exam
    ® MRI Bilateral Breasts (CPT® 77049) if pathology consistent with breast primary and mammogram is inconclusive
    ® If the above are non-diagnostic for primary site:
      ¡ CT Neck (CPT® 70491), CT Chest (CPT® 71260), and CT Abdomen with contrast (CPT® 74160)
      ¡ CT with contrast or MRI without and with contrast of any other symptomatic site
    Above studies have failed demonstrate site of primary® PET/CT (CPT® 78815 or CPT® 78816)
    ONC-31.8: Extrathoracic Small Cell and Large Cell Neuroendocrine Tumors

    For this condition imaging is medically necessary based on the following criteria:

    All poorly-differentiated or high-grade, small cell and large cell neuroendocrine tumors arising outside the lungs or of unknown primary origin are imaged according to these guidelines.
    Indication
    Imaging Study
    Initial stagingAny or all of the following are indicated:
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® MRI Brain without and with contrast (CPT® 70553) should be performed for symptoms of CNS involvement and for poorly differentiated neuroendocrine cancers of the neck or extrapulmonary thorax.
    ® PET/CT (CPT® 78815) if no evidence of metastatic disease or conventional imaging is inconclusive for determining localized vs. distant metastatic disease
    Restaging during treatment® CT Chest (CPT® 71260) and CT Abdomen/Pelvis (CPT® 74177) and any known sites of disease with contrast every 2 cycles
    Suspected RecurrenceAny or all of the following are indicated:
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® MRI brain without and with contrast (CPT® 70553)
    ® Bone scan (See ONC-1.3: Nuclear Medicine (NM) Imaging in Oncology)
    ® PET imaging is generally not indicated but can be considered for rare circumstances. These requests should be forwarded for Medical Director review.
    Surveillance® CT Chest (CPT® 71260) and Abdomen/Pelvis with contrast (CPT® 74177) every 3 months for 1 year, then every 6 months for 4 additional years and then annually
    ONC-31.9: Primary Peritoneal Mesothelioma

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Initial staging® CT Chest (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177)
    ® PET/CT (CPT® 78815) if there is no evidence of metastatic disease or conventional imaging is inconclusive
    Recurrence/ Restaging® If there is known prior disease, CT Chest (CPT® 71260) and Abdomen/Pelvis with contrast (CPT® 74177)
    ® PET for inconclusive finding on conventional imaging
    Surveillance® CT Abdomen/Pelvis with contrast (CPT® 74177) every 3 months for 2 years, then every year of life
    ONC-31.10: Kaposi’s Sarcoma

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Kaposi’s Sarcoma® Advanced imaging is not generally indicated since disease is generally localized to skin.
    ® CT Chest (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177) can be approved at initial diagnosis. If initial scans are negative then future imaging would be based on signs or symptoms.
    ONC-31.11: Castleman’s Disease (Unicentric and Multicentric)

    For this condition imaging is medically necessary based on the following criteria:
    Indication
    Imaging Study
    Initial staging® Either CT Chest (CPT® 71260) and CT Abdomen/Pelvis with contrast (CPT® 74177) or PET/CT (CPT® 78815)
    ® CT Neck with contrast (CPT® 70491) if cervical or supraclavicular involvement
    ® If CT scans were utilized initially and suggested unicentric disease, and surgical resection is being considered, PET/CT (CPT® 78815) can be approved to confirm unicentric disease.
    ® If unicentric disease is surgically removed, proceed to Surveillance section.
    Restaging:
    ® Multicentric disease or surgically unresected unicentric disease on chemotherapy
    One of the following every 2 cycles:
    ® CT Chest (CPT® 71260) and Abdomen/Pelvis with contrast (CPT® 74177)
    ® PET/CT (CPT® 78815)
    Any of the following:
    ® Suspected recurrence
    ® Recurrent B symptoms
    ® Rising LDH/IL-6/VEGF levels
    One of the following:
    ® CT Chest (CPT® 71260) and Abdomen/Pelvis with contrast (CPT® 74177)
    ® PET/CT (CPT® 78815)
    Surveillance® CT with contrast of involved areas no more than every 6 months up to 5 years

    References

    1. Ettinger DS, Varadhachary GR, Bowles DW, et al, National Comprehensive Cancer Network (NCCN) Guidelines Version 2.2019 – January 23, 2019. Occult primary, available at: https://www.nccn.org/professionals/physician_gls/pdf/occult.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for Occult primary V2.2019 – January 23, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    2. Nabors BL, Partnow J, Ammirati M, et al. National Comprehensive Cancer Network (NCCN) Guidelines Version 1.2019 – March 5, 2019. Central Nervous System Cancers, available at: https://www.nccn.org/professionals/physician_gls/pdf/cns.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for CNS tumors Cancer V1.2019 – March 5, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    3. Zelenetz AD, Gordon LI, Wierda WG, et al, National Comprehensive Cancer Network (NCCN) Guidelines Version 4.2019 – June 18, 2019. B-cell lymphomas, available at: https://www.nccn.org/professionals/physician_gls/pdf/B-CELL.pdf Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines™) for B-cell lymphomas V4.2019 – June 18, 2019. ©2019 National Comprehensive Cancer Network, Inc. All rights reserved. The NCCN Guidelines™ and illustrations herein may not be reproduced in any form for any purpose without the express written permission of the NCCN. To view the most recent and complete version of the NCCN Guidelines™, go online to NCCN.org.
    4. Mayo-Smith WM, Song JH, Boland GL, et al. Management of incidental adrenal masses: a white paper of the ACR Incidental Findings Committee. J Am Coll Radiol. 2017;14(8):1038-1044. doi:10.1016/j.jacr.2017.05.001.
    5. ACR Appropriateness Criteria®. Incidentally discovered adrenal mass. Rev. 2012.
    6. Braat AJ, Smits ML, Braat MN, et al. 90Y hepatic radioembolization: an update on current practice and recent developments. J Nucl Med. 2015;56(7):1079–1087. doi:10.2967/jnumed.115.157446.
    7. Pawaskar AS, Basu S. Role of 2-fluoro-2-deoxyglucose PET/computed tomography in carcinoma of unknown primary. PET Clin. 2015;10(3):297-310. doi:10.1016/j.cpet.2015.03.004.
    8. Avram AM. Radioiodine scintigraphy with SPECT/CT: an important diagnostic tool for thyroid cancer staging and risk stratification. J Nucl Med. 2012;53(5): 754-764. doi:10.2967/jnumed.111.104133.


    ONC-32: Medicare Coverage Policies for PET

    ONC-32.1: Oncologic FDG PET
    ONC-32.2: Oncologic Non-FDG PET
    ONC-32.3: Brain PET
    ONC-32.4: Cardiac PET
    ONC-32.5: PET for Infection and Inflammation

    ONC-32.1: Oncologic FDG PET

    For this condition imaging is medically necessary based on the following criteria:

    The complete coverage policy is found in the Medicare National Coverage Determinations (NCD) Manual, Section 220.6.17:
    (see: http://www.cms.gov/Regulations-and-Guidance/Guidance/Manuals/downloads/ncd103c1_Part4.pdf )

    220.6.17 – Positron Emission Tomography (FDG PET) for Oncologic Conditions

    General
    FDG (2-[F18] fluoro-2-deoxy-D-glucose) PET is a minimally invasive diagnostic imaging procedure used to evaluate glucose metabolism in normal tissue, as well as in diseased tissues, in conditions such as cancer, ischemic heart disease, and some neurologic disorders. FDG is an injected radionuclide (or radiopharmaceutical that emits sub-atomic particles, known as positrons, as it decays. FDG PET uses a positron camera (tomograph) to measure the decay of FDG. The rate of FDG decay provides biochemical information on glucose metabolism in the tissue being studied. As malignancies can cause abnormalities of metabolism and blood flow, FDG PET evaluation may indicate the probable presence or absence of a majority of cancer types based upon observed differences in biologic activity compared to adjacent tissues.

    The Centers for Medicare and Medicaid Services (CMS) was asked by the National Oncologic PET Registry (NOPR) to reconsider section 220.6 of the National Coverage Determination (NCD) Manual to end the prospective data collection requirements under Coverage with Evidence Development (CED) across all oncologic indications of FDG PET imaging. The CMS received public input indicating that the current framework of prospective data collection under CED be ended for all oncologic uses of FDG PET imaging

    1. Framework
    Effective for claims with dates of service on and after June 11, 2013, CMS is adopting a coverage framework that ends the prospective data collection requirements by NOPR under CED for all oncologic uses of FDG PET imaging. CMS is making this change for all NCDs that address coverage of FDG PET for oncologic uses addressed in this decision. This decision does not change coverage for any use of PET imaging using radiopharmaceuticals ammonia N-13, or rubidium-82 (Rb-82).

    2. Initial Anti-Tumor Treatment Strategy
    CMS continues to believe that the evidence is adequate to determine that the results of FDG PET imaging are useful in determining the appropriate initial anti-tumor treatment strategy for beneficiaries with suspected cancer and improve health outcomes and thus are reasonable and necessary under §1862(a)(1)(A) of the Social Security Act (the “Act”).

    Therefore, CMS continues to nationally cover ONE FDG PET study for beneficiaries who have cancers that are biopsy proven or strongly suspected based on other diagnostic testing when the beneficiary’s treating physician determines that the FDG PET study is needed to determine the location and/or extent of the tumor for the following therapeutic purposes related to the initial anti-tumor treatment strategy:

    To determine whether or not the beneficiary is an appropriate candidate for an invasive diagnostic or therapeutic procedure; or
    To determine the optimal anatomic location for an invasive procedure; or
    To determine the anatomic extent of tumor when the recommended anti-tumor treatment reasonably depends on the extent of the tumor.
      See the table at the end of this section for a synopsis of all nationally covered and non-covered oncologic uses of FDG PET imaging.
    Initial Anti-Tumor Treatment Strategy Nationally Covered Indication
    Effective: June 11, 2013
    CMS continues to nationally cover FDG PET imaging for the initial anti-tumor treatment strategy for male and female breast cancer only when used in staging distant metastasis.
    CMS continues to nationally cover FDG PET to determine initial anti-tumor treatment strategy for melanoma other than for the evaluation of regional lymph nodes.
    CMS continues to nationally cover FDG PET imaging for the detection of pre-treatment metastasis (i.e., staging) in newly diagnosed cervical cancers following conventional imaging.

    Initial Anti-Tumor Treatment Strategy Nationally Non-Covered Indication
    Effective: June 11, 2013
    CMS continues to nationally non-cover initial anti-tumor treatment strategy in Medicare beneficiaries who have adenocarcinoma of the prostate.
    CMS continues to nationally non-cover FDG PET imaging for diagnosis of breast cancer and initial staging of axillary nodes.
    CMS continues to nationally non-cover FDG PET imaging for initial anti-tumor treatment strategy for the evaluation of regional lymph nodes in melanoma.
    CMS continues to nationally non-cover FDG PET imaging for the diagnosis (no biopsy result) of cervical cancer related to initial anti-tumor treatment strategy.

    3. Subsequent Anti-Tumor Treatment Strategy
    Subsequent Anti-Tumor Treatment Strategy Nationally Covered Indication, Effective: June 11, 2013
    THREE FDG PET scans are nationally covered when used to guide subsequent management of anti-tumor treatment strategy after completion of initial anti-tumor therapy. Coverage of more than three FDG PET scans to guide subsequent management of anti-tumor treatment strategy after completion of initial anti-tumor therapy shall be determined by the local Medicare Administrative Contractors.


    4. Synopsis of Coverage of FDGPET for Oncologic Conditions,
    Effective: June 11, 2013
    Effective for claims with dates of service on and after June 11, 2013, the chart below summarizes national FDG PET coverage for oncologic conditions. Additional details may be obtained at https://www.cms.gov/medicare/coverage/determinationprocess/downloads/petforsolidtumorsoncologicdxcodesattachment_NCD220_6_17.pdf
    FDG PET for Solid Tumors and Myeloma Tumor Type
    Initial Treatment Strategy (formerly “diagnosis” & “staging”)
    Subsequent Treatment Strategy (formerly “restaging” & “monitoring response to) treatment”)
      Colorectal
      Cover
      Cover
      Esophagus
      Cover
      Cover
      Head and Neck
      (not thyroid or CNS)
      Cover
      Cover
      Lymphoma
      Cover
      Cover
      Non-small cell lung
      Cover
      Cover
      Ovary
      Cover
      Cover
      Brain
      Cover
      Cover
      Cervix
      Cover with exceptions
      Cover
      Small cell lung
      Cover
      Cover
      Soft tissue sarcoma
      Cover
      Cover
      Pancreas
      Cover
      Cover
      Testes
      Cover
      Cover
      Prostate
      Non-cover
      Cover
      Thyroid
      Cover
      Cover
      Breast (male and female)
      Cover with exceptions
      Cover
      Melanoma
      Cover with exceptions
      Cover
      All other solid tumors
      Cover
      Cover
      Myeloma
      Cover
      Cover
      All other cancers not listed
      Cover
      Cover
    Invasive Breast Cancer:
    Nationally non-covered for initial diagnosis and/or staging of axillary lymph nodes. Nationally covered for initial staging of known or suspected metastatic disease. All other indications for initial anti-tumor strategy for breast cancer are nationally covered.
    ® Prior to surgical lymph node sampling: NOT indicated
    ® Metastatic disease or suspicious lesions seen on CT and/or bone scan: Indicated
    ® After completion of surgical lymph node sampling in place of CT scans: Indicated
    Melanoma:
    Nationally non-covered for initial staging of regional lymph nodes. All other indications for initial anti-tumor treatment strategy for melanoma are nationally covered.
    ® Prior to surgical lymph node sampling: NOT indicated
    ® Metastatic disease or suspicious lesions seen on CT and/or bone scan: Indicated
    ® After completion of surgical lymph node sampling in place of CT scans: Indicated
    Cervix:
    Nationally non-covered for the initial diagnosis (before biopsy) of cervical cancer related to initial antitumor treatment strategy. All other indications for initial anti-tumor treatment strategy for cervical cancer are nationally covered.

    5. CPT codes for FDG-PET scan for Oncologic Conditions
    The decision whether to use skull base to mid-femur (“eyes to thighs”: procedure code for PET (CPT® 78812 or CPT® 78815) or whole body PET(CPT® 78813 or CPT® 78816) is addressed in the diagnosis-specific guideline sections. Requests requiring CPT® code redirection should be forwarded to Medical Director for review.

    ONC-32.2: Oncologic Non-FDG PET

    For this condition imaging is medically necessary based on the following criteria:

    PET/CT Scan using non-FDG Radiotracers:

    Medicare National Coverage Determination for PET (NCD 220.6.17) has recently included coverage of PET-CT scans with three new non-FDG radiotracers. Local Medicare contractors have the authority to make coverage decisions about oncologic studies performed with other agents.


    PET/CT scan using non-FDG radiotracers is reported with the same CPT codes (CPT® 78815 and CPT® 78816)

    Either FDG or non-FDG PET/CT scan may be approved to assess the disease status, both may not be obtained simultaneously.

    As with FDG PET/CT scan, Medicare NCD allows coverage for ONE non-FDG PET/CT scan for initial anti-tumor strategy (except for newly diagnosed prostate cancer as noted above) and THREE additional non-FDG PET/CT scans for subsequent anti-tumor treatment strategy. Coverage of more than three non-FDG PET/CT scans to guide subsequent management of anti-tumor treatment strategy after completion of initial anti-tumor therapy shall be determined by the local Medicare Administrative Contractors.

    11C Choline for Prostate cancer

    COVERED FOR:

      ® Subsequent treatment strategy for members with prostate cancer who have a rising PSA and have previously been treated with prostatectomy and/or radiation therapy

    NOT COVERED FOR:
      ® Initial treatment strategy for newly diagnosed prostate cancer
      ® Surveillance of members with localized/advanced prostate cancer, who have completed definitive therapy or are receiving maintenance therapy

    18F-Fluciclovine (AXUMIN®) for Prostate cancer

    COVERED FOR:

      ® Subsequent treatment strategy for members with prostate cancer who have a rising PSA and have previously been treated with prostatectomy and/or radiation therapy

    NOT COVERED FOR:
      ® Initial treatment strategy for newly diagnosed prostate cancer
      ® Surveillance of members with localized/advanced prostate cancer, who have completed definitive therapy or are receiving maintenance therapy

    68Gallium DOTATATE (NETSPOT®) for Neuroendocrine tumors

    COVERED FOR:

      ® Initial treatment strategy for newly diagnosed low-grade neuroendocrine tumors
      ® Subsequent treatment strategy for low-grade neuroendocrine tumors

    NOT COVERED FOR:
      ® Surveillance of members with localized/advanced low-grade neuroendocrine tumors, who have completed definitive therapy or are receiving maintenance therapy

    18F Na Fluoride PET/CT Scan for Bone Metastases:

    PET/CT using F-18 sodium fluoride (NaF-18) has been studied to identify bone metastases. At this time, Medicare NCD excludes coverage for PET/CT scan using Na fluoride radiotracer.

    Coverage with Evidence Development (CED):

    CED is a program designed to make PET/CT available to Medicare beneficiaries while at the same time gathering data regarding PET’s effectiveness.

    Under CED, Medicare will reimburse the claim if the beneficiary is enrolled in, and the PET provider is participating in, a qualifying prospective clinical trial or registry.

    Full details regarding qualifying clinical trials, including the list of required scientific integrity standards and relevance to the Medicare population are available in the Medicare NCD Manual, Section 220.6.17.

    Qualifying research trials must be registered on the www.ClinicalTrials.gov website by the principal sponsor/investigator, prior to the enrollment of the first study subject.

    National Oncologic PET Registry (NOPR):

    Providers can meet Medicare’s requirements for CED by submitting PET data to the National Oncologic PET Registry (NOPR).

    A participating hospital or imaging center must submit information to the NOPR for all Medicare PET that falls under CED. This information includes pre- and post-study forms completed by the referring provider, as well as the final radiology report.

    Providers cannot bill Medicare for the services until the NOPR notifies the facility that all required information has been received.

    Imaging facilities cannot submit data to the NOPR for studies performed for covered indications.

    ONC-32.3: Brain PET

    For this condition imaging is medically necessary based on the following criteria:

    CPT® 78608 is used to report FDG PET metabolic brain studies for dementia, seizure disorders, and dedicated PET tumor imaging studies of the brain.

      See ONC-2.2: Low Grade Gliomas and ONC-2.3: High Grade Gliomas for indications of this study.

    CPT® 78609 is used to report PET brain perfusion studies that are not performed with FDG. These scans are nationally noncovered by Medicare.

    CPT® 78811 (Limited PET) or CPT® 78814 (Limited PET/CT hybrid) are used to report Amyloid PET brain studies (these are not metabolic studies).

    Amyloid-beta(Aβ)PET Brain Studies:

      ® Medicare will reimburse for brain PET, performed with the radiopharmaceuticals that detect levels of amyloid in the human brain, only through CED.
      ® Examples of these radiopharmaceuticals include Amyvid™ (florbetapir F18), Neuraceq™ (florbetaben F18) and Vizamyl™ (flutemetamol F18).
      ® CMS will cover one PET Aâ scan per member through CED
      ® For CMS, approval with Coverage with Evidence Development (CED) is available for members enrolled in clinical trials approved by CMS. See the following link for a list of the CMS approved clinical trials: https://www.cms.gov/Medicare/Coverage/Coverage-with-Evidence-Development/Amyloid-PET.html

    FDG PET for Dementia and Neurodegenerative Diseases
      ® Medicare covers FDG PET for individuals with a recent diagnosis of dementia and documented cognitive decline of at least six months who meet diagnostic criteria for both Alzheimer’s disease (AD) and Frontotemporal dementia (FTD).
      ® The individual must have been evaluated for specific alternate neurodegenerative diseases or other causative factors, but the etiology of the symptoms remains unclear.
      ® Other conditions must also be met. For the complete coverage policy, see the Medicare National Coverage Determinations (NCD) Manual, Section 220.6.13*.
      ® Medicare also covers FDG PET for individuals with mild cognitive impairment or early dementia when the study is performed in the context of a CMS-approved clinical trial. Requirements are detailed in Section 220.6.13 of the NCD Manual*.
      ® All other uses of FDG PET for members with a presumptive diagnosis of dementia-causing neurodegenerative disease for which CMS has not specifically indicated coverage continue to be noncovered. Examples of noncovered indications described in the NCD include: possible or probable AD, clinically typical FTD, dementia of Lewy bodies, and Creutzfield-Jacob disease.
        *http://www.cms.gov/Regulations-and-Guidance/Guidance/Manuals/downloads/ncd103c1_Part4.pdf
    FDG PET for Refractory Seizures
    ONC-32.4: Cardiac PET

    For this condition imaging is medically necessary based on the following criteria:

    PET Myocardial Perfusion

      ® Medicare covers PET for myocardial perfusion with rubidium (Rb-82) or ammonia (N-13) when one of the following conditions is met:
        ¡ PET is performed in place of, but not in addition to, a SPECT, or
        ¡ An individual has had an inconclusive SPECT. In these cases, the PET must be considered necessary in order to determine what medical or surgical intervention is required to treat the individual
      ® PET myocardial perfusion is reported with either CPT® 78491 or CPT® 78492.
      ® The complete coverage policy is found in the Medicare National Coverage Determinations (NCD) Manual, Section 220.6.1: http://www.cms.gov/Regulations-and-Guidance/Guidance/Manuals/downloads/ncd103c1_Part4.pdf

    PET Myocardial Viability
      ® Medicare covers FDG PET for myocardial viability as a primary or initial diagnostic study prior to revascularization surgery, or following an inconclusive SPECT scan.
        ¡ The study must be performed on a full or partial ring PET scanner.
        ¡ When PET is performed following an inconclusive SPECT, Medicare will not cover a follow-up SPECT exam if the results of the PET are inconclusive.
        ¡ PET myocardial viability is reported with CPT® 78459.
        ¡ The complete coverage policy is found in the Medicare National Coverage Determinations (NCD) Manual, Section 220.6.8: http://www.cms.gov/Regulations-and-Guidance/Guidance/Manuals/downloads/ncd103c1_Part4.pdf
    ONC-32.5: PET for Infection and Inflammation

    For this condition imaging is medically necessary based on the following criteria:

    Medicare does not cover FDG PET for the following indications:

    Medicare Coverage:
    Medicare Advantage Products follow CMS National Coverage Determinations, Local Coverage Determinations and other CMS Guidance (eg, Medicare Benefit Policy Manual, Medicare Learning Network Articles (MLN Matters Articles), Medicare Claims Processing Manual)). If CMS does not have a coverage or noncoverage position on a service, Medicare Advantage Products will follow Horizon BCBSA Medical Policy. If there is no CMS Guidance and no Horizon BCBSA Policy, then Evicore Diagnostic Advanced Imaging Guidelines will be applied.

    NCDs available to be accessed at CMS National Coverage Determinations (NCDs) Alphabetical Index search page: https://www.cms.gov/medicare-coverage-database/indexes/ncd-alphabetical-index.aspx

    LCDs available to be accessed at Novitas Solutions, Inc., Medical Policy Search page: https://www.novitas-solutions.com/webcenter/portal/MedicareJL/LcdSearch?_afrLoop=90769712476969#!%40%40%3F_afrLoop%3D90769712476969%26centerWidth%3D100%2525%26leftWidth%3D0%2525%26rightWidth%3D0%2525%26showFooter%3Dfalse%26showHeader%3Dfalse%26_adf.ctrl-state%3D63y7eftob_46

    DME LCDS available to be accessed at Noridian Healthcare Services, LLC, (DME MAC), Local Coverage Determinations (LCDs) search page: https://www.cms.gov/medicare-coverage-database/indexes/lcd-list.aspx?Cntrctr=389&ContrVer=1&CntrctrSelected=389*1&s=38&DocType=All&bc=AggAAAAAAAAAAA%3d%3d&#ResultsAnchor.

    Providers are responsible for reviewing CMS Medicare Coverage Center Guidance and in the event of a conflict between the Medicare Coverage section of the medical policy and the CMS Medicare Coverage Center Guidance, the CMS Medicare Coverage Center Guidance will control.

    Medicaid Coverage:

    For members enrolled in Medicaid and NJ FamilyCare plans, Horizon BCBSNJ applies the above medical policy.

    FIDE SNP:

    For members enrolled in a Fully Integrated Dual Eligible Special Needs Plan (FIDE-SNP): (1) to the extent the service is covered under the Medicare portion of the member’s benefit package, the above Medicare Coverage statement applies; and (2) to the extent the service is not covered under the Medicare portion of the member’s benefit package, the above Medicaid Coverage statement applies.

    ________________________________________________________________________________________

    Horizon BCBSNJ Medical Policy Development Process:

    This Horizon BCBSNJ Medical Policy (the “Medical Policy”) has been developed by Horizon BCBSNJ’s Medical Policy Committee (the “Committee”) consistent with generally accepted standards of medical practice, and reflects Horizon BCBSNJ’s view of the subject health care services, supplies or procedures, and in what circumstances they are deemed to be medically necessary or experimental/ investigational in nature. This Medical Policy also considers whether and to what degree the subject health care services, supplies or procedures are clinically appropriate, in terms of type, frequency, extent, site and duration and if they are considered effective for the illnesses, injuries or diseases discussed. Where relevant, this Medical Policy considers whether the subject health care services, supplies or procedures are being requested primarily for the convenience of the covered person or the health care provider. It may also consider whether the services, supplies or procedures are more costly than an alternative service or sequence of services, supplies or procedures that are at least as likely to produce equivalent therapeutic or diagnostic results as to the diagnosis or treatment of the relevant illness, injury or disease. In reaching its conclusion regarding what it considers to be the generally accepted standards of medical practice, the Committee reviews and considers the following: all credible scientific evidence published in peer-reviewed medical literature generally recognized by the relevant medical community, physician and health care provider specialty society recommendations, the views of physicians and health care providers practicing in relevant clinical areas (including, but not limited to, the prevailing opinion within the appropriate specialty) and any other relevant factor as determined by applicable State and Federal laws and regulations.

    ___________________________________________________________________________________________________________________________

    Index:
    Adult Oncology Imaging Policy
    Oncology Imaging Policy, Adult
    Computed Tomography, Oncology, Adult
    CT, Oncology, Adult
    Computed Tomography Angiography, Oncology, Adult
    CTA, Oncology, Adult
    Magnetic Resonance Imaging, Oncology, Adult
    MRI, Oncology, Adult
    Magnetic Resoance Angiography, Oncology, Adult
    MRA, Oncology, Adult
    Positron Emission Tomography, Oncology, Adult
    PET, Oncology, Adult
    Nuclear Medicine Imaging, Oncology, Adult
    Ultrasound, Oncology, Adult
    Gallium-68 Dotatate PET, Adult Oncology Imaging
    NETSPOT™, Adult Oncology Imaging
    Axumin™, Pediatric Oncology Imaging
    Fluorine-18 Fluciclovine PET, Adult Oncology Imaging
    Fluorine-18 Fluorodeoxyglucose PET, Adult Oncology Imaging
    Carbon-11 Choline PET, Adult Oncology Imaging
    18F-FDG PET, Adult Oncology Imaging
    8F-NaF PET, Adult Oncology Imaging
    11C-Choline PET, Adult Oncology Imaging
    68Ga-DOTATATE PET, Adult Oncology Imaging
    Fluciclovine F 18 PET, Adult Oncology Imaging

    References:


    Codes:
    (The list of codes is not intended to be all-inclusive and is included below for informational purposes only. Inclusion or exclusion of a procedure, diagnosis, drug or device code(s) does not constitute or imply authorization, certification, approval, offer of coverage or guarantee of payment.)

    CPT*

      HCPCS

      * CPT only copyright 2020 American Medical Association. All rights reserved. CPT is a registered trademark of the American Medical Association.

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      Medical policies can be highly technical and are designed for use by the Horizon BCBSNJ professional staff in making coverage determinations. Members referring to this policy should discuss it with their treating physician, and should refer to their specific benefit plan for the terms, conditions, limitations and exclusions of their coverage.

      The Horizon BCBSNJ Medical Policy Manual is proprietary. It is to be used only as authorized by Horizon BCBSNJ and its affiliates. The contents of this Medical Policy are not to be copied, reproduced or circulated to other parties without the express written consent of Horizon BCBSNJ. The contents of this Medical Policy may be updated or changed without notice, unless otherwise required by law and/or regulation. However, benefit determinations are made in the context of medical policies existing at the time of the decision and are not subject to later revision as the result of a change in medical policy

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