| Literature DB >> 34625231 |
Vanessa A Fabrizio1, Kevin J Curran2.
Abstract
Chimeric antigen receptor (CAR) T cell therapy has transformed the treatment for both pediatric and adult patients with relapsed or refractory (R/R) B cell acute lymphoblastic leukemia (B-ALL). Clinical trial results across multiple institutions with different CAR constructs report significant response rates in treated patients. One product (tisagenlecleucel) is currently FDA approved for the treatment of R/R B-ALL in patients <26 y/o. Successful application of this therapy is limited by high relapse rates, potential for significant toxicity, and logistical issues surrounding collection/production. Herein, we review published data on the use of CAR T cells for B-ALL, including results from early pivotal clinical trials, relapse data, incidence of toxicity, and mechanisms to optimize CAR T cell therapy.Entities:
Keywords: ALL; Acute lymphoblastic leukemia; Adult; B cell acute lymphoblastic leukemia; B-ALL; CAR; CD19; CD22; Chimeric antigen receptor; Pediatric
Mesh:
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Year: 2021 PMID: 34625231 PMCID: PMC9434884 DOI: 10.1016/j.beha.2021.101305
Source DB: PubMed Journal: Best Pract Res Clin Haematol ISSN: 1521-6926 Impact factor: 3.670