Highmark Commercial Medical Policy - Pennsylvania |
Medical Policy: | R-14-006 |
Topic: | Stereotactic Body Radiation Therapy (SBRT) |
Section: | Radiation Therapy & Nuclear Medicine |
Effective Date: | July 31, 2017 |
Issue Date: | July 31, 2017 |
Last Reviewed: | March 2017 |
Stereotactic body radiotherapy (SBRT) is a fractionated method of stereotactically guided radiation therapy applied over several days, typically to areas of the body other than cranial. SBRT utilizes 3-dimensional conformal radiotherapy method that delivers highly focused, convergent radiotherapy beams on a target that is defined with 3-dimensional imaging techniques with ability to spare adjacent radiosensitive structures. SBRT is used to treat small tumors in the chest, abdomen or tumors that cannot be removed surgically or treated with conventional radiotherapy due to the location. |
This policy is designed to address medical guidelines that are appropriate for the majority of individuals with a particular disease, illness, or condition. Each person's unique clinical circumstances may warrant individual consideration, based on review of applicable medical records.
Policy Position Coverage is subject to the specific terms of the member’s benefit plan. |
Stereotactic body radiation therapy (SBRT) with a radiation source (e.g. gamma knife, cyberknife, or high energy photons generated by a linear accelerator [LINAC] unit ) may be considered medically necessary for localized malignant conditions within the body where highly precise application of high-dose radiotherapy is required to avoid surrounding normal tissue exposure.
Stereotactic body radiation therapy (SBRT) may be considered medically necessary for non-small cell lung cancer when ALL of the following are met:
SBRT is considered experimental/investigational for any other indications not stated above and therefore, non-covered. Scientific evidence does not support the safety and/or effectiveness of this service can be established by the available published peer-reviewed literature for any other indications.
Stereotactic body radiation therapy (SBRT) may be considered medically necessary for primary localized tumors of the liver not amenable to surgery.
SBRT is considered experimental/investigational for any other indications not stated above and therefore is non-covered. Scientific evidence does not support the safety and/or effectiveness of this service can be established by the available published peer-reviewed literature for any other indications.
Stereotactic body radiation therapy (SBRT) may be considered medically necessary for localized prostate cancer when ALL of the following are met:
SBRT is considered experimental/investigational for any other indications not stated above and therefore, non-covered. Scientific evidence does not support the safety and/or effectiveness of this service can be established by the available published peer-reviewed literature for any other indications.
Other Covered Indications
Stereotactic body radiation therapy (SBRT) may be considered medically necessary for:
SBRT is considered experimental/investigational for any other indications not stated above and therefore, non-covered. Scientific evidence does not support the safety and/or effectiveness of this service can be established by the available published peer-reviewed literature for any other indications.
SBRT treatment management (code 77435) is eligible once per course of treatment with the entire course not to exceed five fractions, and includes the work of imaging guidance during treatment.
Stereotactic body radiation therapy (SBRT) with a radiation source (e.g. gamma knife, cyberknife, or high energy photons generated by a linear accelerator [LINAC] unit ) may be considered medically necessary for localized malignant conditions within the body where highly precise application of high-dose radiotherapy is required to avoid surrounding normal tissue exposure
FEP Guidelines
Refer to Medical Policy:
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Place of Service: Outpatient |
Experimental/Investigational (E/I) services are not covered regardless of place of service.
The policy position applies to all commercial lines of business |
Denial Statements |
Services that do not meet the criteria of this policy will be considered experimental/investigational (E/I). A network provider can bill the member for the experimental/investigational service. The provider must give advance written notice informing the member that the service has been deemed E/I. The member must be provided with an estimate of the cost and the member must agree in writing to assume financial responsibility in advance of receiving the service. The signed agreement must be maintained in the provider’s records.
Links |
05/2017, Revised Coverage for Stereotactic Body Radiation Therapy (SBRT)