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:The efficacy and safety of CAR-T therapy in relapsed or refractory multiple myeloma patients: a systematic review and meta-analysis.
The efficacy and safety of CAR-T therapy in relapsed or refractory multiple myeloma patients: a systematic review and meta-analysis.
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新疗法的引入显着改善了多发性骨髓瘤 (MM) 的预后,但复发仍然很常见。对于复发性或难治性多发性骨髓瘤 (RRMM) 患者,免疫疗法 - 特别是CAR-T 细胞 疗法 - 显示出巨大的前景。本综述总结了有关 CAR-T 疗效和安全性的当前证据。
我们对 2021 年 1 月 1 日至 2024 年 8 月 1 日期间在 PubMed、Web of Science 和 Embase 上发表的研究进行了系统回顾。在确定的 4,301 篇文章中,有 29 篇符合纳入标准。
我们的研究结果表明,CAR-T 疗法在治疗 RRMM 方面非常有效,总体缓解率 (ORR) 为 86%。在应答者中,微小残留病 (MRD) 阴性率为 78%。中位无进展生存期(mPFS)为 9.88 个月,中位缓解持续时间(mDOR)为 12.17 个月。就安全性而言,83% 的患者(任何级别)发生细胞因子释放综合征 (CRS),其中 5% 经历 3 级 CRS。 3 级神经毒性 (NT) 的发生率为 2%。 50% 的患者(任何级别)报告感染,其中 21% 经历 3 级感染。
这项荟萃分析为支持 CAR-T 疗法在复发/难治性多发性骨髓瘤治疗中的临床应用提供了强有力的证据。
Objectives: The introduction of novel therapies has markedly improved the prognosis of multiple myeloma (MM), yet relapse remains common. For patients with relapsed or refractory multiple myeloma (RRMM), immunotherapy - particularly chimeric antigen receptor T-cell (CAR-T) therapy - shows significant promise. This review summarizes current evidence on CAR-T efficacy and safety. Methods: We performed a systematic review of studies published between 1 January 2021 and 1 August 2024 in PubMed, Web of Science, and Embase. Of 4,301 articles identified, 29 met inclusion criteria. Results: Our findings demonstrate that CAR-T therapy is highly effective in the treatment of RRMM, with an overall response rate (ORR) of 86%.
Among responders, the minimal residual disease (MRD) negativity rate was 78%. The median progression-free survival (mPFS) was 9. 88 months, and the median duration of response (mDOR) was 12. 17 months. In terms of safety, cytokine release syndrome (CRS) occurred in 83% of patients (any grade), with 5% experiencing grade 3 CRS.
The incidence of grade 3 neurotoxicity (NT) was 2%. Infections were reported in 50% of patients (any grade), with 21% experiencing grade 3 infections. Conclusion: This meta-analysis provides robust evidence supporting the clinical application of CAR-T therapy in the management of relapsed or refractory multiple myeloma.
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