| Literature DB >> 33130313 |
Mark B Leick1, Marcela V Maus2, Matthew J Frigault1.
Abstract
Large B cell lymphoma (LBCL) is curable with standard chemo-immunotherapy in the majority of cases. However, patients with primary refractory or relapsed disease have historically had limited treatment options. Two gene-modified chimeric antigen receptor (CAR)-T cell therapies have now been approved for these indications. The clinical decisions and management surrounding these gene-modified "living drugs" are nuanced and complex. In this article, we discuss the evolving evidence supporting the use of these CAR-T cells, including patient selection, screening procedures, special populations, bridging therapy, lymphodepletion, clinical management, relapse, and follow up.Entities:
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Year: 2020 PMID: 33130313 PMCID: PMC7854294 DOI: 10.1016/j.ymthe.2020.10.022
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454