Initial Approval Criteria
A. Mantle Cell Lymphoma*
(must meet all):
*Only for initial
treatment dose; subsequent doses will not be covered.
1. Diagnosis of relapsed
or refractory MCL;
2. Prescribed by or in
consultation with an oncologist or hematologist;
3. Age ≥ 18 years;
4. Recent (within the
last 30 days) absolute lymphocyte count (ALC) ≥ 100 cells/μL;
5. Member has previously
received 2 to 5 prior regimens that included all of the following (a, b, and c):
a. Anthracycline (e.g., doxorubicin) or bendamustine-containing chemotherapy;
b. Anti-CD20 monoclonal
antibody therapy (e.g., rituximab);
c. Bruton tyrosine kinase
(BTK) inhibitor (e.g., Imbruvica®, Calquence®, Brukinsa™);
6. Member does not have a
history of or current central nervous system (CNS) disease or CNS disorders
(i.e., detectable cerebrospinal fluid malignant cells or brain metastases, CNS
lymphoma, seizure disorder, cerebrovascular ischemia/hemorrhage, dementia,
cerebellar disease, cerebral edema, posterior reversible encephalopathy
syndrome, or any autoimmune disease with CNS involvement);
7. Member does not have a
history of allogeneic stem cell transplantation;
8. Member has not
previously received treatment with CAR T-cell immunotherapy (e.g., Kymriah™,
Yescarta™);
9. Tecartus is not
prescribed concurrently with other CAR T-cell immunotherapy (e.g., Kymriah,
Yescarta);
10. Dose does not exceed
2 x 108
CAR-positive viable T cells/kg.
Approval duration: 3 months (1 dose only, with 4 doses of tocilizumab
(Actemra) at up to 800 mg per dose)
Codes
Used In This BI:
1)
C9073
Brexucabtagene autoleucel, up to 200 million autologous anti-CD19 CAR
positive viable T cells, including leukapheresis and dose preparation
procedures, per therapeutic dose (code deleted & replaced by Q2053 eff 04/01/2021)
2)
Q2053
Brexucabtagene autoleucel, up to 200 million autologous anti-CD19 CAR
positive viable T cells, including leukapheresis and dose preparation
procedures, per therapeutic dose (new code eff 04/01/2021)