嵌合抗原受体
免疫疗法
多发性骨髓瘤
医学
抗原
肿瘤科
免疫学
内科学
免疫系统
作者
Luciano J. Costa,Rahul Banerjee,Hira Mian,Katja Weisel,Susan Bal,Benjamin A. Derman,Myo Htut,Chandramouli Nagarajan,Cesar Rodriguez,Joshua Richter,Matthew J. Frigault,Jing C. Ye,Niels W.C.J. van de Donk,Peter M. Voorhees,Benjamin Puliafito,Nizar J. Bahlis,Rakesh Popat,Wee Joo Chng,P. Joy Ho,Gurbakhash Kaur
出处
期刊:Leukemia
[Springer Nature]
日期:2025-01-27
被引量:9
标识
DOI:10.1038/s41375-024-02482-6
摘要
Abstract T-cell redirecting therapy (TCRT), specifically chimeric antigen receptor T-cell therapy (CAR T-cells) and bispecific T-cell engagers (TCEs) represent a remarkable advance in the treatment of multiple myeloma (MM). There are several products available around the world and several more in development targeting primarily B-cell maturation antigen (BCMA) and G protein–coupled receptor class C group 5 member D (GRPC5D). The relatively rapid availability of multiple immunotherapies brings the necessity to understand how a certain agent may affect the safety and efficacy of a subsequent immunotherapy so MM physicians and patients can aim at optimal sequential use of these therapies. The International Myeloma Working Group conveyed panel of experts to review patient and disease-related factors affecting efficacy and safety of immunotherapy, summarize existing information on sequencing therapy and provide a series of core recommendations.
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