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抗 BCMA CAR-T 细胞治疗多发性骨髓瘤的疗效与安全性探索:系统综述与荟萃分析

英文原题:Exploring the efficacy and safety of anti-BCMA chimeric antigen receptor T-cell therapy for multiple myeloma: Systematic review and meta-analysis.

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Exploring the efficacy and safety of anti-BCMA chimeric antigen receptor T-cell therapy for multiple myeloma: Systematic review and meta-analysis.

PubMed 2024/03/18(内容时间) Cytojournal Q2 · IF 2.2(JCR 2025)

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研究概要

在 MM 中使用抗 BCMA CAR-T 细胞治疗,在降低不良结局以及改善生存结局、完全缓解和总体缓解方面高效且安全。

中文摘要

多发性骨髓瘤(MM)是一种骨髓癌,会显著影响参与免疫应答的浆细胞。骨髓瘤细胞会改变骨髓中各类细胞的正常生成。靶向B细胞成熟抗原(BCMA)的嵌合抗原受体(CAR)T细胞疗法可对患者T细胞进行基因改造,增加CAR表达,使其识别并结合恶性细胞上的BCMA。本研究旨在通过系统综述和荟萃分析,探讨抗BCMA CAR-T 细胞疗法治疗MM的疗效和安全性。

我们检索PubMed、中国知网(CNKI)、EMBASE、Cochrane和Web of Science五个数据库中抗BCMA CAR-T 治疗MM的研究。纳入不同MM治疗阶段的前瞻性单臂研究,可为单中心或多中心;排除非英语出版物和会议论文。所有统计分析均使用R软件和Review Manager 5.4.1完成。

分析共纳入13篇文章。总体缓解和完全缓解率均显著提高。随访后,3–4级细胞因子释放综合征和神经毒性发生率显著降低。然而,微小残留病灶阴性率(MRDN)的降低未达到统计学显著性。

抗BCMA CAR-T 细胞疗法治疗MM疗效高且安全,可减少不良结局,并改善生存、完全缓解和总体应答。

展开英文摘要原文

Multiple myeloma (MM) is a bone marrow cancer that profoundly affects plasma cells involved in the immune response. Myeloma cells alter the average production of cells in the bone marrow. Anti-B-cell maturation antigen (BCMA) chimeric antigen receptor (CAR) T-cell therapy allows genetic modifications of an individual's T-cells to increase the expression of CARs used to identify and attach BCMA proteins to the malignant cells. Our main objective is to perform a systematic review and meta-analysis to explore the efficacy and safety of anti-BCMA CAR T-cell therapy for MM. MATERIAL AND METHODS: We searched five databases, PubMed, CNKI, EMBASE, Cochrane, Web of Science, and CNKI, for studies published on anti-BCMA,CAR-T-cell treatment for MM. Inclusion criteria involved prospective single-arm studies either single or multi-center, in various MM phases and studies that reported anti-BCMA,CAR-T-cell treatment for MM. We excluded non-English publications and conference papers. All statistical analyses were performed in R software and Review Manager 5.4.1.

Thirteen articles were included in the analysis. We found that the overall response survival complete response increase was statistically significant. Similarly, the reduction in cytokine release syndrome grades 3 and 4 and neurotoxicity after follow-up was statistically significant. However, the reduction in minimal residual disease negativity (MRDN) was not statistically significant.

Using anti-BCMA CAR T-cell therapy in MM was highly efficacious and safe in lowering the adverse outcomes and improving the survival outcomes, complete response, and overall response.

论文信息

作者
Zhang J、Ding X、Ding X
第一作者单位
Department of Hematology and Oncology, Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University, Taizhou, China.China
通讯作者单位
Department of Hematology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, China.China
期刊
CytoJournal2024
原文标识
PubMed 38628287 · DOI 10.25259/Cytojournal_64_2023