Prior authorization request form Form
Selective Internal Radiation Therapy
Last Review Date: May 8, 2026
Number: MG.MM.RA.12dC5Medical Guideline Disclaimer
The treating physician or primary care provider must submit to EmblemHealth the clinical evidence that the member meets the criteria for
the treatment or surgical procedure. Without this documentation and information, EmblemHealth will not be able to properly review the
request preauthorization or post-payment review. The clinical review criteria expressed below reflects how EmblemHealth determines
whether certain services or supplies are medically necessary. This clinical policy is not intended to pre-empt the judgment of the reviewing
medical director or dictate to health care providers how to practice medicine. Health care providers are expected to exercise their medical
judgment in rendering appropriate care. Health care providers are expected to exercise their medical judgment in rendering appropriate care.
EmblemHealth established the clinical review criteria based upon a review of currently available clinical information (including clinical
outcome studies in the peer reviewed published medical literature, regulatory status of the technology, evidence-based guidelines of public
health and health research agencies, evidence-based guidelines and positions of leading national health professional organizations, views of
physicians practicing in relevant clinical areas, and other relevant factors). EmblemHealth expressly reserves the right to revise these
conclusions as clinical information changes and welcomes further relevant information. Each benefit program defines which services are
covered. The conclusion that a particular service or supply is medically necessary does not constitute a representation or warranty that this
service or supply is covered and/or paid for by EmblemHealth, as some programs exclude coverage for services or supplies that EmblemHealth
considers medically necessary.
If there is a discrepancy between this guideline and a member's benefits program, the benefits program will govern. Identification of selected
brand names of devices, tests and procedures in a medical coverage policy is for reference only and is not an endorsement of any one device,
test or procedure over another. In addition, coverage may be mandated by applicable legal requirements of a state, the Federal Government
or the Centers for Medicare & Medicaid Services (CMS) for Medicare and Medicaid members. All coding and web site links are accurate at
time of publication.
EmblemHealth may also use tools developed by third parties, such as the MCG™ Care Guidelines, to assist us in administering health benefits.
The MCG™ Care Guidelines are intended to be used in connection with the independent professional medical judgment of a qualified health
care provider and do not constitute the practice of medicine or medical advice. EmblemHealth Services Company, LLC, has adopted this policy
in providing management, administrative and other services to EmblemHealth Plan, Inc., EmblemHealth Insurance Company, EmblemHealth
Services Company, LLC, and Health Insurance Plan of Greater New York (HIP) related to health benefit plans offered by these entities. All of
the aforementioned entities are affiliated companies under common control of EmblemHealth Inc.
Definition
Selective Internal Radiation Therapy (SIRT) — also referred to as radioembolization or yttrium-90 (Y-90)
hepatic brachytherapy, is an outpatient transcatheter interventional technique whereby radioactive
particles (Y-90 microspheres) are delivered directly to the liver tumor bed via the hepatic artery. Once
implanted, the microspheres emit localized radiation.
FDA-approved radioactive microspheres include SIR-Spheres® (biocompatible) and TheraSphere®
(insoluble glass).
Guideline
I.
Selective internal radiation therapy (SIRT) is considered medically necessary when the following
criteria are met:
A. Unresectable and/or medically inoperable primary or metastatic liver malignancies
- Unresectable liver only or liver dominant metastases from neuroendocrine tumors (e.g., carcinoids, pancreatic islet cell tumors, endocrine (tumor)
- Unresectable primary hepatocellular carcinoma (HCC)
- Unresectable metastatic liver tumors from primary colorectal cancer
- Treatment of unresectable liver metastases from breast carcinoma, ocular melanoma, cutaneous melanoma, or intrahepatic cholangiocarcinoma in the absence of available
systemic or liver-directed treatment options to relieve symptoms and/or possibly extend
life expectancy
B. The tumor burden should be liver dominant, not necessarily exclusive to the liver
C. Eastern Cooperative Oncology Group (ECOG) performance status should be 0 or 1 or Karnofsky
Performance Status (KPS) of 70 or more
D. Life expectancy should be at least 3 months
E. Radioactive Yttrium-90 (90Y) microspheres treatment is allowed only in the outpatient setting
unless the documentation supports the medical necessity of inpatient treatment
II. Repeat radioembolization is considered medically necessary for new or progressive primary or
metastatic liver cancers when:
A. The member has had a previous satisfactory response to an initial radioembolization treatment
as evidenced on results of a computed tomography (CT) scan or positron emission tomography
(PET)-CT scan performed 3 months following the previous procedure. Response should be graded
according to the revised RECIST guideline (Version 1.1)
B. The disease still must be liver dominant
C. Life expectancy of at least 3 months
D. ECOG performance status no greater than 2 or KPS of 70 or more
E. There are no other effective systemic or liver-directed treatment options
F. The member has compensated liver function tests (LFTs)
G. Estimated lung dose and combined lung dose from previous embolizations are within acceptable
dose volume constraints. Exclude an individual with lung shunting in which the lung radiation dose
is greater than 25 to 30 Gy per treatment or greater than 50 Gy cumulatively for all treatments
H. Treatment should be given to a targeted tumor volume
I.
Repeat whole liver irradiation is considered experimental, investigational, or unproven (EIU) and
will not be certified
J. Requests for a third radioembolization will not be certified
K. All requests for repeat radioembolization are subject to medical review
Limitations/Exclusions
Only FDA-approved microspheres will be considered medically necessary.
Requests for the treatment of liver metastases from other primary malignancies, including breast
carcinoma, ocular melanoma, cutaneous melanoma, and intrahepatic cholangiocarcinoma, will be
considered on a case-by-case basis. These requests should be based on the lack of any known systemic or
liver-directed treatment options for the member in an effort to relieve symptoms and/or possibly extend
life expectancy.
Radioactive Yttrium-90 (90Y) microspheres treatment is allowed only in the outpatient setting unless the
documentation supports the medical necessity of inpatient treatment.
Revision History May 7, 2021 Added covered indication for treatment of unresectable liver metastases from breast carcinoma, ocular melanoma, cutaneous melanoma, or intrahepatic cholangiocarcinoma Mar. 8, 2019 Added repeat radioembolization criteria Oct. 9, 2015 Added ECOG performance score prerequisite and life expectancy language Aug. 20, 2009 Added hepatoma
Applicable Procedure Codes
37243
Vascular embolization or occlusion, inclusive of all radiological supervision and interpretation,
intraprocedural roadmapping, and imaging guidance necessary to complete the intervention; for tumors,
organ ischemia, or infarction
75894
Transcatheter therapy, embolization, any method, radiological supervision and interpretation
77778
Interstitial radiation source application; complex
79445
Radiopharmaceutical therapy, by intra-arterial particulate administration
Q3001
Radioelements for brachytherapy, any type, each
S2095
Transcatheter occlusion or embolization for tumor destruction, percutaneous, any method, using
yttrium-90 microspheres
Applicable ICD-10 Diagnosis Codes
C22.0
Liver cell carcinoma C22.1 Intrahepatic bile duct carcinoma C22.2 Hepatoblastoma C22.3 Angiosarcoma of liver C22.4 Other sarcomas of liver C22.7 Other specified carcinomas of liver C22.8 Malignant neoplasm of liver, primary, unspecified as to type C22.9 Malignant neoplasm of liver, not specified as primary or secondary C78.7 Secondary malignant neoplasm of liver and intrahepatic bile duct References
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