← 返回

复发/难治性多发性骨髓瘤患者 CAR-T 治疗失败后的挽救治疗策略

英文原题:Strategies for salvage therapy post CAR-T therapy failure in refractory/relapsed multiple myeloma patients.

查看英文原题

Strategies for salvage therapy post CAR-T therapy failure in refractory/relapsed multiple myeloma patients.

PubMed 2025/03/17(内容时间) Front Pharmacol Q1 · IF 5.4(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

过去数十年,多发性骨髓瘤(MM)治疗领域显著进步,主要受益于新一代蛋白酶体抑制剂(PI)和免疫调节药物(IMiD)的批准及应用。尽管如此,MM 仍无法治愈。2021 年 3 月,美国 FDA 批准CAR-T 细胞疗法 idecabtagene vicleucel(ide-cel)治疗复发/难治性多发性骨髓瘤(R/R MM),由此开启 R/R MM 细胞疗法时代。然而,由于肿瘤抗原表达下调或丢失、T 细胞耗竭以及肿瘤免疫微环境的影响,多数 R/R MM 患者接受 CAR-T 治疗后仍不可避免地复发。因此,CAR-T 后挽救治疗已成为关键研究领域。本综述讨论导致 R/R MM 患者 CAR-T 治疗失败的潜在因素,并介绍后续挽救治疗策略,为应对此类治疗失败提供建议。

展开英文摘要原文

Over the past few decades, the landscape for multiple myeloma (MM) therapy has significantly advanced, largely due to the approval and introduction of new-generation proteasome inhibitors (PIs) and immunomodulatory drugs (IMiDs). Despite these advancements, MM remains incurable. In March 2021, the U. S. FDA approved the chimeric antigen receptor T-cell (CAR-T) therapy idecabtagene vicleucel (ide-cel) for relapsed/refractory multiple myeloma (R/R MM), heralding the advent of cellular therapies for R/R MM.

However, due to factors such as the downregulation or loss of tumor antigen expression, T-cell exhaustion, and the influence of the tumor immune microenvironment, most R/R MM patients inevitably experience relapse following CAR-T cell therapy.

Consequently, salvage therapy in the post-CAR-T setting has emerged as a critical area of research. This review discusses the potential factors leading to CAR-T therapy failure in R/R MM patients and discusses subsequent salvage therapeutic strategies, offering recommendations for addressing treatment failure in this context.

论文信息

作者
Min C、Zhong X、Cui Y、Zhang H、Wang Q
单位
Department of Hematology, 2nd Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxin, China.China
文献类型
综述
期刊
Frontiers in pharmacology2025
原文标识
PubMed 40166474 · DOI 10.3389/fphar.2025.1515555