Proton pump inhibitors and outcome after axicabtagene ciloleucel for the treatment of non-Hodgkin B-cell lymphoma, a retrospective study with the DESCAR-T registry

Axicabtagene ciloleucel (axi-cel), an autologous anti-CD19 chimeric antigen receptor CAR T-cell (CAR-T), is a major second- or third-line treatment in refractory or early relapsed large B-cell lymphoma (LBCL), primary mediastinal large B-cell lymphoma (PMBL) and follicular lymphoma (FL) [ 1 ]. Although axi-cel induces high complete response rates in relapsed or refractory LBCL, PMBL, and FL, relapse remains the leading cause of treatment failure. Long-term follow-up from ZUMA-1 and ZUMA-5 demonstrates that most progression events occur within the first years after CAR-T infusion [ 2 , 3 ]. Adverse events include cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), and infections, associated with increased morbidity and mortality. Understanding the determinants underlying toxicity and relapse is crucial to improve patient outcomes, optimize treatment strategies, and reducing disease burden.

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Publication Details

Journal
Bone Marrow Transplantation
Published
2026-11-06
DOI
https://doi.org/10.1038/s41409-026-03076-9
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00

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article

Proton pump inhibitors and outcome after axicabtagene ciloleucel for the treatment of non-Hodgkin B-cell lymphoma, a retrospective study with the DESCAR-T registry

Elodie Gat, Jérôme Paillassa, Aline Schmidt, Roch Houot et al.
1 links
Bone Marrow Transplantation
CAR-T cell therapy research
article

Proton pump inhibitors and outcome after axicabtagene ciloleucel for the treatment of non-Hodgkin B-cell lymphoma, a retrospective study with the DESCAR-T registry

Elodie Gat, Jérôme Paillassa, Aline Schmidt, Roch Houot, Niels Moya, Martin Eloit, Eva Desbrousses, Stéphanie Guidez, Nicolas Vallet, Thomas Gastinne, Benoît Tessoulin, Vivien Dupont, Thierry Lamy de La Chapelle, Emmanuel Gyan
article en

Abstract

Axicabtagene ciloleucel (axi-cel), an autologous anti-CD19 chimeric antigen receptor CAR T-cell (CAR-T), is a major second- or third-line treatment in refractory or early relapsed large B-cell lymphoma (LBCL), primary mediastinal large B-cell lymphoma (PMBL) and follicular lymphoma (FL) [ 1 ]. Although axi-cel induces high complete response rates in relapsed or refractory LBCL, PMBL, and FL, relapse remains the leading cause of treatment failure. Long-term follow-up from ZUMA-1 and ZUMA-5 demonstrates that most progression events occur within the first years after CAR-T infusion [ 2 , 3 ]. Adverse events include cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), and infections, associated with increased morbidity and mortality. Understanding the determinants underlying toxicity and relapse is crucial to improve patient outcomes, optimize treatment strategies, and reducing disease burden.

Bone Marrow Transplantation
Université de Tours (FR), Inserm (FR), Centre Hospitalier Universitaire de Nantes (FR), Centre Hospitalier Universitaire de Tours (FR), The Lymphoma Academic Research Organisation (FR), Centre Hospitalier Universitaire de Poitiers (FR), Centre Hospitalier Universitaire d'Angers (FR), Centre Hospitalier Universitaire de Rennes (FR), Niche, Nutrition, Cancer et métabolisme oxydatif (FR)
Centre Hospitalier Universitaire de Rennes
Good health and well-being
Openalex Percentile: Top 16%
CAR-T cell therapy research
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