Role of bridging therapy during chimeric antigen receptor T cell therapy
- PMID: 35844303
- PMCID: PMC9175845
- DOI: 10.1002/jha2.335
Role of bridging therapy during chimeric antigen receptor T cell therapy
Abstract
Chimeric antigen receptor (CAR) T-cell therapy has been approved for use in several relapsed/refractory hematologic malignancies and has significantly improved outcomes for these diseases. A number of different CAR T products are now being used in clinical practice and have demonstrated excellent outcomes to those in clinical trials. However, increased real-world use of CAR T therapy has uncovered a number of barriers that can lead to significant delays in treatment. As a result, bridging therapy has become a widely used tool to stabilize or debulk disease between leukapheresis and CAR T cell administration. Here we review the available data regarding bridging therapy, with a focus on patient selection, choice of therapy, timing of therapy, and potential pitfalls.
Keywords: bridging therapy; chimeric antigen receptor T cell therapy; hematologic malignancies.
© 2021 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd.
Conflict of interest statement
STB, SMS and BNS report no COI. BRD reports institutional funding from Takeda, Janssen, Angiocrine, Pfizer, Poseida, MEI, Sorrento. Consultancy with Jazz, Celgene, Gamida Cell. OOO reports advisory board consultancy with Pfizer, Novartis, Janssen, Kite, Gilead, Spectrum, Bayer and Curio science. Research funding with Kite.
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