bosutinib — CareFirst (Caremark)
Philadelphia chromosome-positive (Ph+) B-cell acute lymphoblastic leukemia (B-ALL) or lymphoblastic lymphoma (B-LL)
Initial criteria
- Diagnosis of Ph+ B-ALL or Ph+ B-LL confirmed by detection of Ph chromosome or BCR::ABL gene by cytogenetic and/or molecular testing
- ANY of the following:
- • Member has not received prior therapy with a tyrosine kinase inhibitor (TKI) (e.g., dasatinib, imatinib, nilotinib, ponatinib)
- • Member experienced intolerance or toxicity to prior therapy with a TKI
- • Member experienced resistance to prior therapy with a TKI and results of BCR::ABL1 mutation testing are negative for all of the following: T315I, G250E, V299L, and F317L
- • Member has received HSCT for Ph+ B-ALL/LL and results of BCR::ABL1 mutation testing are negative for all of the following: T315I, G250E, V299L, and F317L
Reauthorization criteria
- No evidence of unacceptable toxicity or disease progression while on the current regimen
- AND either:
- • Ph+ B-ALL/LL confirmed by detection of Ph chromosome or BCR::ABL gene by cytogenetic and/or molecular testing, OR
- • Member has received HSCT for B-ALL/LL
Approval duration
Initial 12 months; Reauthorization 12 months