医学
内科学
临床试验
细胞因子释放综合征
荟萃分析
人口
嵌合抗原受体
免疫疗法
癌症
环境卫生
作者
Othman Salim Akhtar,Ba Aqeel Sheeba,Farhan Azad,Lauren Alessi,Doris K. Hansen,Melissa Alsina,Rachid Baz,Kenneth H. Shain,Ariel Grajales Cruz,Omar Castañeda Puglianini,Hien Liu,Brandon Blue,Taiga Nishihori,Mohammed Al Jumayli,Martine Extermann,Frederick L. Locke,Rahul Mhaskar,Ciara L. Freeman
标识
DOI:10.1016/j.jgo.2023.101628
摘要
Introduction Anti-B-cell maturation antigen (BCMA) chimeric antigen receptor T-cell (CAR-T) therapy is transforming the care of patients with relapsed/refractory multiple myeloma (MM). Unfortunately, despite being a disease of older adults these patients remain under-represented in most pivotal clinical trials. We performed a systematic review and proportion meta-analysis of prospective clinical trials and observational studies of anti-BCMA CAR-T therapy in patients with MM with the aim to determine the efficacy and safety of this therapy in older adults (≥65 years). Materials and Methods We searched the Pubmed, Scopus, Web of Science (WOS), Ovid, Embase, CENTRAL, and CINAHL databases through September 9, 2022 and abstracts from the American Society of Hematology (ASH) Annual Meeting 2022. Primary outcome measures included overall response rate (ORR), rates of cytokine release syndrome (CRS), and immune cell-effector-associated neurotoxicity syndrome (ICANS). study was registered with PROSPERO (study number: CRD42022334287). Results After screening 2218 references, 14 studies were included for data extraction, with a total of 558 patients, 26.2% (n = 146) of whom were older adults. The pooled ORR amongst this population was 93%, which was comparable to the ORR of 86% amongst younger patients. In older adults, the rates of CRS (any grade) and grade ≥ 3 were 95% and 21%, respectively. For younger patients, the pooled rate of CRS (any grade) and grade ≥ 3 CRS was 91% and 20%, respectively. The rate of ICANS (any grade) in older adults was 15%, which was higher than that observed in those <65 years. Conclusion Older adults experience comparable outcomes to younger patients with anti-BCMA CAR-T therapy, albeit with numerically higher rates of neurotoxicity.
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