| Literature DB >> 31320380 |
Matthew J Frigault1,2, Jorg Dietrich1,3, Maria Martinez-Lage4, Mark Leick1, Bryan D Choi1,5, Zachariah DeFilipp1,2, Yi-Bin Chen1,2, Jeremy Abramson1,6, Jennifer Crombie7, Philippe Armand7, Lakshmi Nayak7, Chris Panzini1, Lauren S Riley1, Kathleen Gallagher1, Marcela V Maus1,2.
Abstract
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.Entities:
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Year: 2019 PMID: 31320380 PMCID: PMC7022436 DOI: 10.1182/blood.2019001694
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 25.476