Abstract
The U.S. Food and Drug Administration (FDA) approved 6 CAR T cell (CAR-T) products, including tisagenlecleucel (tisa-cel), axicabtagene ciloleucel (axi-cel), brexucabtagene autoleucel (brexu-cel), lisocabtagene maraleucel (liso-cel), idecabtagene vicleucel (ide-cel), and ciltacabtagene autoleucel (cilta-cel) in the last 5 years. CAR T-cell therapy significantly improved outcomes for patients with B-cell non-Hodgkin lymphoma (NHL) and multiple myeloma (MM). However, recurrence and progression may occur after the initial response due to multiple mechanisms (Zeng and Zhang, 2022) [1]. Furthermore, CAR T-cell therapy is not broadly utilized in solid tumors due to various barriers. This review discusses the evolution of CAR T-cell therapies and how the “younger-generation” CAR T cells counteract these challenges to potentially broaden their applications in the future.
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CITATION STYLE
Yi, D., Gergis, M., Hsu, J., Yang, Y., Bi, X., Aljurf, M., & Gergis, U. (2022). Next-Generation Chimeric Antigen Receptor T-cells. Hematology/ Oncology and Stem Cell Therapy, 15(3), 117–121. https://doi.org/10.56875/2589-0646.1035
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