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CAR-T 细胞治疗多发性骨髓瘤:我们身在何处,以及需要什么才能推动 CAR-T 细胞前移至更早的治疗线?美国移植与细胞治疗学会专家小组意见

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.

查看英文原题

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.

PubMed 2023/10/31(内容时间) Transplant Cell Ther Q1 · IF 4.7(JCR 2025)

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中文摘要

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。

展开英文摘要原文

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.

论文信息

作者
Anderson LD Jr、Dhakal B、Jain T、Oluwole OO、Shah GL、Sidana S、Perales MA、Pasquini MC
单位
Myeloma, Waldenstrom's, and Amyloidosis Program, Hematologic Malignancies and Cellular Therapy Program, Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas. Electronic address: Larry.Anderson@UTSouthwestern.edu.United States
文献类型
综述 · 临床实践指南 · 美国 NIH 资助研究
期刊
Transplantation and cellular therapy2024 Jan
原文标识
PubMed 37913909 · DOI 10.1016/j.jtct.2023.10.022