Practical Aspects of Immunotherapy: A Report from the 20th International Myeloma Society (IMS) Annual Meeting

被引:1
|
作者
Raje, Noopur S. [1 ,7 ]
Cohen, Adam D. [2 ]
Patel, Krina K. [3 ]
van de Donk, Niels W. C. J. [4 ]
Richter, Joshua [5 ]
San-Miguel, Jesus [6 ]
机构
[1] Massachusetts Gen Hosp, Div Hematol Oncol, Canc Ctr, Boston, MA USA
[2] Univ Penn, Abramson Canc Ctr, Philadelphia, PA USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Lymphoma & Myeloma, Div Canc Med, Houston, TX USA
[4] Vrije Univ Amsterdam, Canc Ctr Amsterdam, Dept Hematol, Amsterdam UMC, Amsterdam, Netherlands
[5] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY USA
[6] Univ Navarra, Canc Ctr Clin, CIMA, IDISNA,CIBERONC, Pamplona, Spain
[7] Massachusetts Gen Hosp, Ctr Multiple Myeloma, Canc Ctr, Boston, MA 02114 USA
关键词
Lymphoma; Myeloma Leukemia; 24; 6; rights Bispecific antibody; Chimeric antigen receptor T cells; Multiple myeloma; T-cell engager; T-CELL THERAPY; MULTIPLE-MYELOMA; RISK; INFECTION; EFFICACY; SAFETY;
D O I
10.1016/j.clml.2024.03.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The 20th annual IMS meeting dedicated a session to the practical aspects regarding T-cell redirected therapies, specifically chimeric antigen receptor T-cell (CAR-T) therapies and bispecific antibodies/T-cell engagers (bsAbs/TCEs), an increasing number of which have been introduced recently into the relapsed/refractory MM (RRMM) treatment landscape. This article summarizes the discussions and key take-home messages from this session. Immunotherapeutic strategies, specifically T-cell-redirected therapies, have been transformative in the context of multiple myeloma (MM). With the approval of two chimeric antigen receptor T-cell (CAR-T) drug products and three bispecific antibodies/T-cell engagers (bsAbs/TCEs) in relapsed/refractory MM (RRMM), the 20th annual IMS meeting dedicated a session to the practical aspects of these therapies. Here, we highlight the discussion during this session, including the role of CAR-T and bsAb therapies in frontline MM treatment, management of acute toxicities, prevention and management of infections, and finally treatment sequencing of T-cell redirected therapies.
引用
收藏
页码:350 / 357
页数:8
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