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:An Assessment of the Effectiveness and Safety of Chimeric Antigen Receptor T-Cell Therapy in Multiple Myeloma Patients with Relapsed or Refractory Disease: A Systematic Review and Meta-Analysis.
An Assessment of the Effectiveness and Safety of Chimeric Antigen Receptor T-Cell Therapy in Multiple Myeloma Patients with Relapsed or Refractory Disease: A Systematic Review and Meta-Analysis.
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多发性骨髓瘤(MM)是第二常见的血液系统恶性肿瘤,目前仍无法治愈,且发病率不断上升。CAR-T 细胞(CAR-T 细胞)疗法已成为一种新型治疗手段,有望改善复发/难治性多发性骨髓瘤(rrMM)患者的生存率和生活质量。在本系统综述和荟萃分析中,我们按照PRISMA指南进行,旨在简要概述CAR-T 疗法的最新进展,评估其临床实践的潜在意义,并基于最新证据评价其疗效和安全性结局。在Medline/PubMed、Scopus和Web of Science上对2019年1月1日至2023年7月12日期间进行的文献检索共识别出2273篇文章,其中29篇符合规定的纳入标准。
我们的结果提供了强有力的证据支持CAR-T 细胞疗法在rrMM患者中的疗效,总缓解率(ORR)令人鼓舞,达83.21%。观察到总体安全性良好,3级细胞因子释放综合征(CRS)为7.12%,3级神经毒性为1.37%。亚组分析显示,抗骨髓瘤治疗方案较少的患者ORR显著升高,而3级CRS在高危细胞遗传学比例较高和既往接受过BCMA治疗的患者中更为常见。
Multiple myeloma (MM), the second most common hematologic malignancy, remains incurable, and its incidence is rising. Chimeric Antigen Receptor T-cell (CAR-T cell) therapy has emerged as a novel treatment, with the potential to improve the survival and quality of life of patients with relapsed/refractory multiple myeloma (rrMM).
In this systematic review and meta-analysis, conducted in accordance with PRISMA guidelines, we aim to provide a concise overview of the latest developments in CAR-T therapy, assess their potential implications for clinical practice, and evaluate their efficacy and safety outcomes based on the most up-to-date evidence. A literature search conducted from 1 January 2019 to 12 July 2023 on Medline/PubMed, Scopus, and Web of Science identified 2273 articles, of which 29 fulfilled the specified criteria for inclusion.
Our results offer robust evidence supporting CAR-T cell therapy's efficacy in rrMM patients, with an encouraging 83. 21% overall response rate (ORR). A generally safe profile was observed, with grade 3 cytokine release syndrome (CRS) at 7. 12% and grade 3 neurotoxicity at 1. 37%. A subgroup analysis revealed a significantly increased ORR in patients with fewer antimyeloma regimens, while grade 3 CRS was more common in those with a higher proportion of high-risk cytogenetics and prior exposure to BCMA therapy.
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