Xospata (gilteritinib) — CareFirst (Caremark)
FLT3 mutation-positive AML as maintenance therapy post-allogeneic hematopoietic cell transplantation
Initial criteria
- Medical record documentation of FLT3 and IDH1 mutation status, where applicable
- For FLT3 mutation-positive AML without IDH1 mutation, Xospata may be used as a single agent or in combination with azacitidine in any of the following: induction therapy if not a candidate for or declines intensive induction therapy; post-induction therapy when there is response to Xospata therapy
- For FLT3 mutation-positive AML, Xospata may be used as a single agent in any of the following: maintenance therapy post-allogeneic hematopoietic cell transplantation; relapsed or refractory disease
- For myeloid and/or lymphoid neoplasms with eosinophilia with FLT3 rearrangement, Xospata may be used in chronic phase or blast phase
Reauthorization criteria
- Member continues treatment for an indication listed in the coverage criteria
- No evidence of unacceptable toxicity or disease progression while on Xospata therapy
Approval duration
12 months