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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