학술논문

Optimal Dual-Targeted CAR Construct Simultaneously Targeting Bcma and GPRC5D Prevents Bcma-Escape Driven Relapse in Multiple Myeloma
Document Type
Article
Source
Blood; November 2019, Vol. 134 Issue: 1, Number 1 Supplement 1 p136-136, 1p
Subject
Language
ISSN
00064971; 15280020
Abstract
Multiple myeloma (MM) remains generally incurable, calling for the development of novel treatment strategies such as chimeric antigen receptor (CAR) T cell therapy. Most clinically tested CAR T cell therapies for MM target B cell maturation antigen (BCMA), but despite high response rates, many patients relapse (Raje N. NEJM2019). BCMA negative-low MM cells are implicated as a reservoir preceding relapse (Brudno J. JCO2018; Cohen A. JCI2019). Our aims are to (1) evaluate whether upfront simultaneous targeting of an additional antigen such as G protein-coupled receptor class C group 5 member D (GPRC5D; Smith EL. Sci Trans Med2019) can mitigate BCMA escape-mediated relapse in MM, and (2) compare dual targeting strategies to identify an optimal approach.