Tisagenlecleucel CAR T-cell therapy in secondary CNS lymphoma.
Matthew J FrigaultJorg DietrichMaria Martinez-LageMark B LeickBryan D ChoiZachariah DeFilippYi-Bin ChenJeremy S AbramsonJennifer CrombiePhilippe ArmandLakshmi NayakChris PanziniLauren S RileyKathleen GallagherMarcela V MausPublished in: Blood (2019)
Chimeric antigen receptor (CAR) T cells targeting CD19 have emerged as a leading engineered T-cell therapy for relapsed/refractory B-cell non-Hodgkin lymphoma. The phase 1/2 clinical trials that led to US Food and Drug Administration approval excluded patients with central nervous system (CNS) involvement, due to strict eligibility criteria. Here, we report on our institutional experience with 8 secondary CNS lymphoma patients treated with commercial tisagenlecleucel. No patient experienced greater than grade 1 neurotoxicity, and no patient required tocilizumab or steroids for CAR T-cell-mediated toxicities. Biomarker analysis suggested CAR T-cell expansion, despite the absence of systemic disease, and early response assessments demonstrated activity of IV infused CAR T cells within the CNS space.
Keyphrases
- cell therapy
- drug administration
- blood brain barrier
- diffuse large b cell lymphoma
- clinical trial
- case report
- rheumatoid arthritis
- stem cells
- mesenchymal stem cells
- acute myeloid leukemia
- rheumatoid arthritis patients
- cancer therapy
- systemic lupus erythematosus
- hodgkin lymphoma
- bone marrow
- drug delivery
- study protocol