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The International Prognostic Index Is Associated with Outcomes in Diffuse Large B Cell Lymphoma after Chimeric Antigen Receptor T Cell Therapy.

Authors :
Garcia-Recio M
Wudhikarn K
Pennisi M
Alonso-Trillo R
Flynn J
Shouval R
Afuye AO
Silverberg ML
Batlevi CW
Dahi P
Devlin S
Giralt SA
Halton E
Ruiz J
Maloy M
Mead E
Palomba ML
Santomasso B
Sauter CS
Scordo M
Shah GL
Perales MA
Source :
Transplantation and cellular therapy [Transplant Cell Ther] 2021 Mar; Vol. 27 (3), pp. 233-240. Date of Electronic Publication: 2020 Dec 18.
Publication Year :
2021

Abstract

CD19-targeted chimeric antigen receptor (CAR) T cells have shown excellent activity against relapsed and refractory (R/R) diffuse large B cell lymphoma (DLBCL). CAR T cell therapy is associated with early toxicities, including cytokine release syndrome and neurotoxicity. The incidence and severity of these toxicities has been associated in part with baseline disease and patient characteristics, which also may impact overall survival (OS) and progression-free survival (PFS). However, there are limited data on patient selection and how to better predict toxicities or outcomes. Indexes used in patients with DLBCL, such as the International Prognostic Index (IPI and age-adjusted IPI [aaIPI]) and in transplantation recipients, such as the Hematopoietic Cell Transplantation Comorbidity Index (HCT-CI), have not been evaluated in this setting. Here we evaluated 4 indices- IPI, aaIPI, HCT-CI, and the Charlson Comorbidity Index (CCI)-and their associations with early CAR T cell related-toxicities and outcomes. We demonstrated an association between high-risk IPI or aaIPI and inferior PFS in patients with R/R DLBCL treated with CAR T cell therapy. We also found an association between aaIPI and IPI with OS and neurotoxicity, respectively. CCI was not associated with toxicities or outcomes, and owing to the small sample size, we could not draw a conclusion regarding associations with the HCT-CI. Both the IPI and aaIPI are widely used tools that can now provide better information to guide selection of patients who would best benefit from CD19 CAR T cell therapy.<br /> (Copyright © 2020 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2666-6367
Volume :
27
Issue :
3
Database :
MEDLINE
Journal :
Transplantation and cellular therapy
Publication Type :
Academic Journal
Accession number :
33781518
Full Text :
https://doi.org/10.1016/j.jtct.2020.10.022