Highmark Commercial Medical Policy - Pennsylvania |
Medical Policy: | I-124-003 |
Topic: | Azacitidine (Vidaza®) |
Section: | Injections |
Effective Date: | July 30, 2018 |
Issue Date: | July 30, 2018 |
Last Reviewed: | April 2018 |
Azacitidine (Vidaza®) is a pyrimidine nucleoside used as an antineoplastic agent. The drug disrupts the chemistry of DNA and causes cellular death in rapidly dividing cells, including cancer cells that no longer respond to normal growth control mechanism. |
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. |
Intravenous or subcutaneous use of azacitidine (Vidaza) may be considered medically necessary for ANY ONE of the following indications:
Myelofibrosis
Acute Myeloid Leukemia (AML):
Myelodysplastic Syndromes (MDS):
Azacitidine (Vidaza) is considered experimental/investigational for all other indications. Peer reviewed literature does not support the use of azacitidine (Vidaza) for any indications other than those listed on this medical policy.
Dosage recommendations per the FDA label. *Note: Language derived from National Comprehensive Cancer Network (NCCN) guidelines Note: Lower risk defined as IPSS-R (Very Low, Low, Intermediate), IPSS (Low/Intermediate-1), WPSS (Very Low, Low, Intermediate). Higher risk defined as IPSS-R (Intermediate, High, Very High), IPSS (Intermediate-2, High), WPSS (High, Very High). |
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 |
02/2016, Revised Policy Guidelines For Azacitidine (Vidaza)
05/2018, Coverage Guidelines Revised for Azacitidine (Vidaza)