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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Strategies for salvage therapy post CAR-T therapy failure in refractory/relapsed multiple myeloma patients.
Strategies for salvage therapy post CAR-T therapy failure in refractory/relapsed multiple myeloma patients.
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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。
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.
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