Phase 1 studies of central memory–derived CD19 CAR T–cell therapy following autologous HSCT in patients with B-cell NHL

Author:

Wang Xiuli1,Popplewell Leslie L.1,Wagner Jamie R.1,Naranjo Araceli1,Blanchard M. Suzette2,Mott Michelle R.3,Norris Adam P.3,Wong ChingLam W.1,Urak Ryan Z.1,Chang Wen-Chung1,Khaled Samer K.1,Siddiqi Tanya1,Budde Lihua E.1,Xu Jingying1,Chang Brenda1,Gidwaney Nikita4,Thomas Sandra H.1,Cooper Laurence J. N.5,Riddell Stanley R.6,Brown Christine E.1,Jensen Michael C.7,Forman Stephen J.1

Affiliation:

1. Department of Hematology and Hematopoietic Cell Transplantation,

2. Department of Information Sciences,

3. Clinical Trials Unit, and

4. Department of Radiology, City of Hope, Duarte, CA;

5. Division of Pediatrics, University of Texas MD Anderson Cancer Center, Houston, TX;

6. Program in Immunology, Fred Hutchinson Cancer Research Center, Seattle, WA; and

7. Ben Towne Center for Childhood Cancer Research, Seattle Children’s Research Institute and School of Medicine, Seattle, WA

Abstract

Key Points TCM-derived CD19 CAR T–cell therapy is safe for treatment of poor-risk NHL patients undergoing autologous HSCT. Addition of a CD28 costimulatory domain to the CAR, plus changes to T-cell product manufacturing, resulted in improved T-cell expansion.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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