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CAR-T 细胞免疫治疗多发性骨髓瘤关键时间点性能分析的系统综述

英文原题:A systematic review on performance analysis of critical time points in multiple myeloma treated by CAR-T cell immunotherapy.

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A systematic review on performance analysis of critical time points in multiple myeloma treated by CAR-T cell immunotherapy.

PubMed 2022/12/20(内容时间) Int Immunopharmacol Q1 · IF 5.6(JCR 2025)

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研究概要

本系统综述总结了 CAR-T 疗法在 MM 中疗效和安全性相关指标的中位检测时间点,并构建了时间相关的 CAR-T 治疗平台,为 MM 中 CAR-T 治疗方案的建立提供了循证标准。

研究思路结论见上方概要

多发性骨髓瘤(MM)是第二常见的血液系统恶性肿瘤,无法治愈,而CAR-T 细胞疗法在MM中显示出巨大前景。与以往主要关注疗效和安全性的已发表研究不同,本研究旨在总结MM中CAR-T 治疗过程中的时间点,并建立标准化的时间相关CAR-T 治疗平台,为MM的CAR-T 治疗提供参考。

所有文献均从PubMed、Web of Science、Embase、美国血液学会(ASH)、美国临床肿瘤学会(ASCO)和欧洲血液学协会(EHA)检索获得。从纳入文献中提取CAR-T 疗法治疗MM的疗效和安全性相关指标的中位检测时间,并应用中位值代表指标的检测时间点。值得注意的是,中位值并非确定且最佳的检测时间点,其意义在于围绕中位值可更频繁地检测指标以获得理想结果。

本综述按时间顺序呈现了CAR-T 治疗MM中疗效和安全性相关指标的中位检测时间点。对于CAR-T 开始后1个月内对炎症状态的短期影响,细胞因子释放综合征发作、免疫效应细胞相关神经毒性综合征发作、中性粒细胞恢复和CAR-T 扩增峰值的中位时间点分别为4.5、8、10和12天。对于CAR-T 输注后超过1个月至3个月对MM临床反应的中期影响,微小残留病阴性、血清轻链降至最低、血小板恢复和M蛋白降至最低的中位时间点分别为30、30、44和90天。

展开英文摘要原文

Multiple myeloma (MM) is the second most common hematological malignancy without cure, and Chimeric Antigen Receptor T Cell (CAR-T) therapy has been shown great promising in MM. Unlike previous published studies mainly focusing on efficacy and safety, this study aims to summarize time points in the process of CAR-T therapy in MM and establish a standardized time-related CAR-T therapy platform to provide a reference for CAR-T treatment in MM.

All the literatures were retrieved from PubMed, Web of Science, Embase, American Society of Hematology (ASH), American Society of Clinical Oncology (ASCO) and European Hematology Association (EHA). Relevant median detection time of efficacy and safety-related indicators of CAR-T therapy in MM were extracted from included literatures, and median values were applied to represent detection time points of indicators. Notably, the median values were not the certain and optimal detection time points, while the significance is that indicators could be detected more frequently around the median values to obtain the ideal results.

This review presented the median detection time points of efficacy and safety-related indicators of CAR-T therapy in MM according to the chronological order. For short-term effects on inflammation status within 1 month after CAR-T initiation, the median time points of cytokine release syndrome onset, immune effector cell-associated neurotoxicity syndrome onset, neutrophils recovery and CAR-T expansion peak were 4.5, 8, 10 and 12 days, respectively. For medium-term effects on clinical response in MM beyond 1 month and up to 3 months following CAR-T infusion, the median time points of minimal residual disease negativity, the reduction of serum light chain to minimum, platelet recovery and the reduction of M protein to minimum were 30, 30, 44 and 90 days, respectively.

This systematic review summarized the median detection time points of efficacy and safety-related indicators of CAR-T therapy in MM and constructed the time-related CAR-T therapy platform, providing an evidence-based standard for establishment of CAR-T treatment regimen in MM.

论文信息

作者
Zhang Y、Tang W、Li Y、Yi Y、Yu Z、Liu X、Zhang L、Zheng Y
第一作者单位
Department of Hematology, Institute of Hematology, West China Hospital, Sichuan University, #37 Guo Xue Xiang Street, 610041 Chengdu, China.China
通讯作者单位
Department of Hematology, Institute of Hematology, West China Hospital, Sichuan University, #37 Guo Xue Xiang Street, 610041 Chengdu, China. Electronic address: zhengyuhuan@scu.edu.cn.China
文献类型
系统综述
期刊
International immunopharmacology2023 Jan
原文标识
PubMed 36700772 · DOI 10.1016/j.intimp.2022.109592