Zhang Yue, Tang Wenjiao, Li Yan, Yi Yuyao, Yu Zhengyu, Liu Xiang, Zhang Li, Zheng Yuhuan, Niu Ting
Department of Hematology, Institute of Hematology, West China Hospital, Sichuan University, #37 Guo Xue Xiang Street, 610041 Chengdu, China.
Department of Hematology, Institute of Hematology, West China Hospital, Sichuan University, #37 Guo Xue Xiang Street, 610041 Chengdu, China; Clinical Trial Center, National Medical Products Administration Key Laboratory for Clinical Research and Evaluation of Innovative Drugs, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China.
Int Immunopharmacol. 2023 Jan;114:109592. doi: 10.1016/j.intimp.2022.109592. Epub 2022 Dec 20.
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.
多发性骨髓瘤(MM)是第二常见的无法治愈的血液系统恶性肿瘤,嵌合抗原受体T细胞(CAR-T)疗法在MM治疗中显示出巨大潜力。与以往主要关注疗效和安全性的研究不同,本研究旨在总结MM患者CAR-T治疗过程中的时间节点,并建立标准化的CAR-T治疗时间相关平台,为MM的CAR-T治疗提供参考。
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)检索所有文献。从纳入的文献中提取MM患者CAR-T治疗疗效和安全性相关指标的相关中位检测时间,并用中位数值代表指标的检测时间点。值得注意的是,这些中位数值并非确定的最佳检测时间点,其意义在于在中位数值附近更频繁地检测指标,以获得理想结果。
本综述按时间顺序呈现了MM患者CAR-T治疗疗效和安全性相关指标的中位检测时间点。对于CAR-T启动后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天、8天、10天和12天。对于CAR-T输注后1个月以上至3个月内对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天、30天、44天和90天。
本系统综述总结了MM患者CAR-T治疗疗效和安全性相关指标的中位检测时间点,并构建了CAR-T治疗时间相关平台,为MM患者CAR-T治疗方案的制定提供了循证标准。