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[Eligibility of patients for CAR T-cell: Expert opinion-based collaborative work by the SFGM-TC].

Authors :
Beauvais D
Bachy E
Baruchel A
Bay JO
Caillot D
Cartron G
Damaj G
Furst S
Le Gouill S
Morschhauser F
Rabian F
Rubio MT
Thieblemont C
Yakoub-Agha I
Source :
Bulletin du cancer [Bull Cancer] 2021 Jul-Aug; Vol. 108 (7-8), pp. 725-729. Date of Electronic Publication: 2021 Jan 07.
Publication Year :
2021

Abstract

The chimeric antigen receptor T-cells are a new class of anticancer treatment consisting in genetically modifying autologous or allogenic T-cells to make express a CAR directed against a membrane tumor antigen. In Europe, tisagenlecleucel (Kymriah <superscript>TM</superscript> ) has a marketing authorization for the treatment of relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia in children and young adults and of R/R diffuse large B-cell lymphoma (DLBCL). The marketing authorization for axicabtagene ciloleucel (Yescarta <superscript>TM</superscript> ) is the treatment of DLBCL and primary R/R mediastinal B-cell lymphoma. The two products are autologous T-cells directed against CD19. This collaborative work, part of a series of expert opinion-based work, aims to give practical advice to help centers in selection of patients for commercially available CAR T-cell treatment.<br /> (Copyright © 2020 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.)

Details

Language :
French
ISSN :
1769-6917
Volume :
108
Issue :
7-8
Database :
MEDLINE
Journal :
Bulletin du cancer
Publication Type :
Academic Journal
Accession number :
33423776
Full Text :
https://doi.org/10.1016/j.bulcan.2020.10.017