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,Prashant Kapoor,Juan Du,Fredrik Schjesvold,Jesús G. Berdeja,Hermann Einsele,Adam D. Cohen,Joseph Mıkhael,Yelak Biru,S. Vincent Rajkumar,Yi Lin,Thomas G. Martin,Ajai Chari
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.