CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Chimeric Antigen Receptor T Cell Therapy for Myeloma: Where Are We Now and What Is Needed to Move Chimeric Antigen Receptor T Cells Forward to Earlier Lines of Therapy? Expert Panel Opinion from the American Society for Transplantation and Cellular Therapy.
Chimeric Antigen Receptor T Cell Therapy for Myeloma: Where Are We Now and What Is Needed to Move Chimeric Antigen Receptor T Cells Forward to Earlier Lines of Therapy? Expert Panel Opinion from the American Society for Transplantation and Cellular Therapy.
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自2021年以来,美国食品药品监督管理局(FDA)已批准两种靶向B细胞成熟抗原(BCMA)的CAR-T 细胞疗法——idecabtagene vicleucel(ide-cel)和ciltacabtagene autoleucel(cilta-cel),用于既往至少接受4线治疗(包括免疫调节药、蛋白酶体抑制剂和抗CD38抗体)的复发/难治性多发性骨髓瘤(RRMM)。这两种产品在RRMM中显示前所未有的活性,但复发仍很常见;对于进展迅速的晚期患者,CAR-T 治疗的可及性和安全性也不理想。由于数据显示既往接受BCMA靶向治疗后再用CAR-T 疗法结局较差,如何将CAR-T 与其他治疗(包括近期获批的两种BCMA靶向T细胞接合双特异性抗体teclistamab和elranatamab)排序,变得日益困难。
因此,人们开始考虑在骨髓瘤病程较早阶段使用CAR-T,此时患者T细胞可能更健康,骨髓瘤侵袭性也较低。针对CAR-T 早期应用问题,目前已有多项试验正在开展或计划启动;近期报告的两项随机试验显示,CAR-T 疗法用于二线(CARTITUDE-4)或三线(KarMMA-3)治疗时,无进展生存期优于标准治疗。鉴于FDA可能将CAR-T 批准范围扩展至骨髓瘤较早治疗线次,美国移植与细胞治疗学会召集专家组,全面回顾促成CAR-T 获批用于骨髓瘤晚期治疗的研究,讨论旨在将治疗前移的近期报告及正在开展的研究,并分享当前实践中BCMA靶向治疗的排序及患者筛选优化方面的见解和考量。
Since 2021, 2 B cell maturation antigen (BCMA)-directed chimeric antigen receptor T cell (CAR-T) therapies-idecabtagene vicleucel (ide-cel), and ciltacabtagene autoleucel (cilta-cel)-have been approved by the US Food and Drug Administration (FDA) for treating relapsed or refractory multiple myeloma (RRMM) after 4 or more prior lines of therapy, including an immunomodulatory drug, a proteasome inhibitor, and an anti-CD38 antibody. The 2 products have shown unprecedented activity in RRMM, but relapses remain common, and access to and safety of CAR-T therapy in patients with rapidly progressing advanced disease are not ideal. Sequencing CAR-T therapy with other options, including the 2 recently approved BCMA-directed T cell-engaging bispecific antibodies teclistamab and elranatamab, has become increasingly challenging owing to data showing inferior outcomes from CAR-T therapy after prior BCMA-directed therapy.
This has led to the consideration of CAR-T therapy earlier in the course of disease for myeloma, when T cells are potentially healthier and the myeloma is less aggressive. To address the question of earlier use of CAR-T therapy, several trials are either ongoing or planned, and results have recently been reported for 2 randomized trials of CAR-T therapy showing improved progression-free survival compared to standard of care therapy in second-line (CARTITUDE-4) or third-line therapy (KarMMA-3).
With the anticipation of the FDA possibly expanding approval of CAR-T to earlier lines of myeloma therapy, the American Society for Transplantation and Cellular Therapy convened a group of experts to provide a comprehensive review of the studies that led to the approval of CAR-T therapy in late-line therapy for myeloma, discuss the recently reported and ongoing studies designed to move CAR-T therapy to earlier lines of therapy, and share insights and considerations for sequencing therapy and optimization of patient selection for BCMA-directed therapies in current practice.
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