Brukinsa (zanubrutinib) — CareFirst (Caremark)
Mantle cell lymphoma (MCL)
Initial criteria
- Member is an adult (age ≥ 18 years).
- Brukinsa will be used as a single agent when the member has received at least one prior therapy OR
- Brukinsa will be used as a component of TRIANGLE regimen for members with TP53 mutations for induction therapy (TRIANGLE regimen = alternating RCHOP [rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone] + Brukinsa/RDHAP [rituximab, dexamethasone, and cytarabine] + platinum [carboplatin, cisplatin, or oxaliplatin] regimen) OR
- Brukinsa will be used in combination with rituximab for pre-induction therapy or maintenance therapy OR
- Brukinsa will be used as induction therapy for TP53 mutated disease in combination with Venclexta (venetoclax) and Gazyva (obinutuzumab).
Reauthorization criteria
- No evidence of unacceptable toxicity or disease progression while on the current regimen.
Approval duration
12 months