Stereotactic Body Radiation Therapy (SBRT) and Stereotactic Radiosurgery (SRS) Coverage Criteria
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Defines medical necessity criteria and coding guidance for up to five sessions of SBRT and SRS for specified indications for members/enrollees of the health plan.
No material clinical or coverage changes in this revision.
Coverage Criteria for SBRT and SRS
SBRT - Medically Necessary Indications (up to 5 sessions)
Covered when ANY ONE of the following indications is met:
SRS - Medically Necessary Indications (up to 5 sessions)
Covered when ANY ONE of the following indications is met:
Limit on number of sessions
Covered only up to specified number of sessions:
Covered indications (high-level)
Policy includes coverage criteria and has been updated to add or clarify the following indications
Full nesting and granular criteria (performance status, lesion size, dose/fractionation) are detailed in other sections of the policy.
There is insufficient evidence to recommend SBRT for most head and neck cancers; it may be considered only for limited palliative indications or in select older adults where other options are not appropriate. When using SBRT techniques for reirradiation in the head and neck region, avoid treating patients with circumferential carotid involvement due to increased risk, and preferentially select smaller tumors without skin involvement for better outcomes.
The policy text was refined to remove redundant examples and to reword certain indications for clarity. For example, the criteria for cranial non-neoplastic conditions were reorganized and the example of trigeminal neuralgia was removed from one subsection where it was already listed elsewhere. These edits do not change the clinical intent of the criteria but improve readability and alignment with current guidance.
Per policy review, there is no evidence to support use of more than five sessions/fractions of SBRT or SRS for indications other than those specifically enumerated in the coverage criteria; requests exceeding this limit are not supported by the evidence cited in the policy.
Language previously using the term 'experimental/investigational' has been replaced with descriptive wording in the criteria to specify when treatments are not supported by sufficient evidence. Conditions now described as not medically necessary are those for which the policy states there is insufficient evidence (for example, courses beyond five fractions for non‑listed indications); the policy identifies these as not supported by current evidence rather than using the experimental/investigational label.
Coding and Billing Guidance
| 61796 | Stereotactic radiosurgery; 1 simple cranial lesion |
| 61797 | Each additional cranial lesion, simple |
| 61798 | Stereotactic radiosurgery; 1 complex cranial lesion |
| 61799 | Each additional cranial lesion, complex |
| 61800 | Application of stereotactic headframe for stereotactic radiosurgery |
| 63620 | Stereotactic radiosurgery; 1 spinal lesion |
| 63621 | Each additional spinal lesion |
| 77371 | Radiation treatment delivery, SRS, cranial lesion(s), 1 session; multi-source Cobalt 60 based |
| 77372 | Radiation treatment delivery, SRS, cranial lesion(s), 1 session; linear accelerator based |
| 77373 | Stereotactic body radiation therapy, treatment delivery, per fraction to 1 or more lesions, entire course not to exceed 5 fractions |
| G0339 | Image guided robotic linear accelerator-based stereotactic radiosurgery, complete course of therapy in one session or first session of fractionated treatment |
| G0340 | Image guided robotic linear accelerator-based stereotactic radiosurgery, fractionated treatment, per session, second through fifth sessions, maximum five sessions per course |
| G0563 | Stereotactic body radiation therapy, treatment delivery, per fraction to 1 or more lesions, including image guidance and real-time position emissions-based delivery adjustments, entire course not to exceed 5 fractions |
Provider Actions, Authorization, and Documentation
Prior Authorization Required
Prior authorization is required for stereotactic body radiation therapy (SBRT) and stereotactic radiosurgery (SRS) courses described in this policy. Requests should follow the Health Plan’s established prior authorization procedures and be submitted before services are rendered when possible. Courses of treatment up to five fractions/sessions will be reviewed against the policy criteria; requests for more than five sessions for indications not specifically enumerated in the policy are not supported by the evidence summarized in this policy and may be denied.
- Providers must obtain authorization per the Health Plan’s procedures prior to initiation of treatment when required.
- Requests exceeding five fractions/sessions should include supporting clinical rationale and are at increased risk for denial.
Documentation Expectations
Documentation submitted with authorization requests and claims must demonstrate how the requested SBRT/SRS meets the policy indications and clinical criteria. Include relevant history, imaging reports, pathology, prior treatment records (including prior radiation fields and doses), performance status (Karnofsky or ECOG), tumor size/location details, and a treatment plan specifying dose per fraction, total dose, and modality (e.g., linac-based, Gamma Knife, robotic). For recurrent disease or retreatment, provide prior radiation dosimetry and justification for stereotactic approach.
- Provide imaging and reports that show lesion size, location relative to critical structures, and absence or extent of metastatic disease as applicable.
- Include documentation of multidisciplinary discussion or tumor board review when available, and clinical rationale when SBRT/SRS is used as an alternative to other therapies.
Coding and Billing Guidance
Providers must follow current professional coding guidance when submitting claims. CPT, HCPCS and other codes listed in this policy are informational and not exhaustive. Inclusion or exclusion of codes here does not guarantee coverage. Verify and use the most up-to-date CPT/HCPCS descriptors and modifiers, and append appropriate modifiers indicating laterality, multiple procedures, or staged treatments as required by coding rules.
- Reference current CPT guidance prior to claim submission; codes in the policy (e.g., 77373, 77435, 61796-61800 series, 63620-63621, G0339-G0340, G0563) are examples and not guaranteed to be all-inclusive.
- When billing for fractionated courses, ensure the course-level vs per-fraction codes are applied correctly and that image-guidance or robotic delivery descriptors are supported by documentation.
Consideration of Alternative Therapies
Consideration should be given to alternative therapies and sequencing of care. For some indications (for example early-stage non-small cell lung cancer, hepatocellular carcinoma, pancreatic cancer, and prostate cancer) SBRT/SRS may be offered as an alternative to surgery, ablation, embolization, or conventionally fractionated external beam radiation therapy when clinically appropriate. Document why SBRT/SRS is preferred or necessary (e.g., medical inoperability, prior therapies failed or contraindicated, patient refusal of surgery, or to provide palliation).
- When SBRT/SRS is used as an alternative, provide documentation of contraindications to or failure of other standard therapies, or evidence of multidisciplinary consensus supporting the selected approach.
- For pancreatic SBRT, consider referral to or treatment at high-volume centers with image-guided capability; avoid SBRT when direct invasion of bowel or stomach is present on imaging.
Denial Risk and Appeals
Coverage determinations are subject to all terms, conditions, exclusions, and limitations of the member’s benefit plan. Failure to provide required documentation, use of incorrect or outdated codes, or provision of services outside the policy criteria may result in denial. Providers may appeal adverse determinations per the Health Plan’s established appeal processes.
- Denials commonly result from insufficient documentation of indication, lack of prior authorization when required, requests for treatment courses exceeding five fractions without compelling evidence, or billing with inappropriate codes/modifiers.
- Review applicable state Medicaid, Medicare NCDs/LCDs, and the member’s benefit contract; when conflicts exist, state Medicaid provisions or Medicare determinations take precedence for respective members.
Background and Clinical Context
Stereotactic radiosurgery (SRS) and stereotactic body radiation therapy (SBRT) are highly conformal, high‑dose radiation techniques that deliver treatment to precise targets while minimizing dose to surrounding tissues. SBRT is typically used for extracranial sites and is generally delivered in 1–5 fractions, whereas SRS is most often used for intracranial or spinal targets and may be delivered as a single session or up to five sessions for select indications. These therapies require specialized localization and delivery systems and are generally provided by multidisciplinary teams at experienced centers.
Definitions and Terminology
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