Venclexta (venetoclax) — Highmark
Acute Myeloid Leukemia (AML)
Initial criteria
- age ≥ 18 years
- newly diagnosed AML (ICD-10 C92.0)
- Venclexta used in combination with azacitidine OR decitabine OR low-dose cytarabine
- member has at least one comorbidity that precludes use of intensive induction chemotherapy defined as one of the following: age ≥ 75 years OR severe cardiac or pulmonary comorbidity OR reduced renal function OR hepatic impairment OR prescriber attests that member is not a candidate for intensive induction therapy
Reauthorization criteria
- prescriber attests that the member is tolerating therapy AND has experienced a therapeutic response defined as either disease improvement OR delayed disease progression
Approval duration
12 months