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Severe cytopenia after CD19 CAR T-cell therapy: a retrospective study from the EBMT Transplant Complications Working Party

We investigated the incidence and outcome of anti-CD19 chimeric antigen receptor (CAR) T-cells-associated Common Terminology Criteria for Adverse Events (CTCAE) ≥grade 3 cytopenia. In the EBMT CAR-T registry, we identified 398 adult patients with large B-cell lymphoma who had been treated with CAR-T...

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Autores principales: Penack, Olaf, Peczynski, Christophe, Koenecke, Christian, Polge, Emmanuelle, Kuhnl, Andrea, Fegueux, Nathalie, Daskalakis, Michael, Kröger, Nicolaus, Dreger, Peter, Besley, Caroline, Schanz, Urs, Bloor, Adrian, Ganser, Arnold, Forcade, Edouard, Corral, Lucia López, Passweg, Jakob R, Novak, Urban, Moiseev, Ivan, Schoemans, Hélène, Basak, Grzegorz W, Chabannon, Christian, Sureda, Anna, Averbuch, Dina, Glass, Bertram, de la Camara, Rafael, Peric, Zinaida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124318/
https://www.ncbi.nlm.nih.gov/pubmed/37072350
http://dx.doi.org/10.1136/jitc-2022-006406
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author Penack, Olaf
Peczynski, Christophe
Koenecke, Christian
Polge, Emmanuelle
Kuhnl, Andrea
Fegueux, Nathalie
Daskalakis, Michael
Kröger, Nicolaus
Dreger, Peter
Besley, Caroline
Schanz, Urs
Bloor, Adrian
Ganser, Arnold
Forcade, Edouard
Corral, Lucia López
Passweg, Jakob R
Novak, Urban
Moiseev, Ivan
Schoemans, Hélène
Basak, Grzegorz W
Chabannon, Christian
Sureda, Anna
Averbuch, Dina
Glass, Bertram
de la Camara, Rafael
Peric, Zinaida
author_facet Penack, Olaf
Peczynski, Christophe
Koenecke, Christian
Polge, Emmanuelle
Kuhnl, Andrea
Fegueux, Nathalie
Daskalakis, Michael
Kröger, Nicolaus
Dreger, Peter
Besley, Caroline
Schanz, Urs
Bloor, Adrian
Ganser, Arnold
Forcade, Edouard
Corral, Lucia López
Passweg, Jakob R
Novak, Urban
Moiseev, Ivan
Schoemans, Hélène
Basak, Grzegorz W
Chabannon, Christian
Sureda, Anna
Averbuch, Dina
Glass, Bertram
de la Camara, Rafael
Peric, Zinaida
author_sort Penack, Olaf
collection PubMed
description We investigated the incidence and outcome of anti-CD19 chimeric antigen receptor (CAR) T-cells-associated Common Terminology Criteria for Adverse Events (CTCAE) ≥grade 3 cytopenia. In the EBMT CAR-T registry, we identified 398 adult patients with large B-cell lymphoma who had been treated with CAR-T-cells with axicel (62%) or tisacel (38%) before August 2021 and had cytopenia status documented for the first 100 days. Most patients had received two or three previous lines of therapy, however, 22.3% had received four or more. Disease status was progressive in 80.4%, stable in 5.0% and partial/complete remission in 14.6%. 25.9% of the patients had received a transplantation before. Median age was 61.4 years (min–max; IQR=18.7–81; (52.9–69.5)). The cumulative incidence of ≥grade 3 cytopenia was 9.0% at 30 days (95% CI (6.5 to 12.1)) and 12.1% at 100 days after CAR T-cell infusion (95% CI (9.1 to 15.5)). The median time from CAR-T infusion to cytopenia onset was 16.5 days (min–max; IQR=1–90; (4–29.8)). Grade 3 and grade 4 CTCAE cytopenia occurred in 15.2% and 84.8%, respectively. In 47.6% there was no resolution. Severe cytopenia had no significant impact on overall survival (OS) (HR 1.13 (95% CI 0.74 to 1.73), p=0.57). However, patients with severe cytopenia had a poorer progression-free survival (PFS) (HR 1.54 (95% CI 1.07 to 2.22), p=0.02) and a higher relapse incidence (HR 1.52 (95% CI 1.04 to 2.23), p=0.03). In those patients who developed severe cytopenia during the first 100 days (n=47), OS, PFS, relapse incidence and non-relapse mortality at 12 months after diagnosis of severe cytopenia were 53.6% (95% CI (40.3 to 71.2)), 20% (95% CI (10.4 to 38.6)), 73.5% (95% CI (55.2 to 85.2)) and 6.5% (95% CI (1.7 to 16.2)), respectively. In multivariate analysis of severe cytopenia risk factors, only year of CAR-T infusion (HR=0.61, 95% CI (0.39 to 0.95), p=0.028) and total number of treatment lines before CAR-T infusion (one or two lines vs three or more, HR=0.41, 95% CI (0.21 to 0.83), p=0.013) had a significant positive association with the incidence of cytopenia. Other factors, such as previous transplantation, disease status at time of CAR-T, patient age and patient sex, had no significant association. Our data provide insight on frequency and clinical relevance of severe cytopenia after CAR T-cell therapy in the European real-world setting.
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spelling pubmed-101243182023-04-25 Severe cytopenia after CD19 CAR T-cell therapy: a retrospective study from the EBMT Transplant Complications Working Party Penack, Olaf Peczynski, Christophe Koenecke, Christian Polge, Emmanuelle Kuhnl, Andrea Fegueux, Nathalie Daskalakis, Michael Kröger, Nicolaus Dreger, Peter Besley, Caroline Schanz, Urs Bloor, Adrian Ganser, Arnold Forcade, Edouard Corral, Lucia López Passweg, Jakob R Novak, Urban Moiseev, Ivan Schoemans, Hélène Basak, Grzegorz W Chabannon, Christian Sureda, Anna Averbuch, Dina Glass, Bertram de la Camara, Rafael Peric, Zinaida J Immunother Cancer Immune Cell Therapies and Immune Cell Engineering We investigated the incidence and outcome of anti-CD19 chimeric antigen receptor (CAR) T-cells-associated Common Terminology Criteria for Adverse Events (CTCAE) ≥grade 3 cytopenia. In the EBMT CAR-T registry, we identified 398 adult patients with large B-cell lymphoma who had been treated with CAR-T-cells with axicel (62%) or tisacel (38%) before August 2021 and had cytopenia status documented for the first 100 days. Most patients had received two or three previous lines of therapy, however, 22.3% had received four or more. Disease status was progressive in 80.4%, stable in 5.0% and partial/complete remission in 14.6%. 25.9% of the patients had received a transplantation before. Median age was 61.4 years (min–max; IQR=18.7–81; (52.9–69.5)). The cumulative incidence of ≥grade 3 cytopenia was 9.0% at 30 days (95% CI (6.5 to 12.1)) and 12.1% at 100 days after CAR T-cell infusion (95% CI (9.1 to 15.5)). The median time from CAR-T infusion to cytopenia onset was 16.5 days (min–max; IQR=1–90; (4–29.8)). Grade 3 and grade 4 CTCAE cytopenia occurred in 15.2% and 84.8%, respectively. In 47.6% there was no resolution. Severe cytopenia had no significant impact on overall survival (OS) (HR 1.13 (95% CI 0.74 to 1.73), p=0.57). However, patients with severe cytopenia had a poorer progression-free survival (PFS) (HR 1.54 (95% CI 1.07 to 2.22), p=0.02) and a higher relapse incidence (HR 1.52 (95% CI 1.04 to 2.23), p=0.03). In those patients who developed severe cytopenia during the first 100 days (n=47), OS, PFS, relapse incidence and non-relapse mortality at 12 months after diagnosis of severe cytopenia were 53.6% (95% CI (40.3 to 71.2)), 20% (95% CI (10.4 to 38.6)), 73.5% (95% CI (55.2 to 85.2)) and 6.5% (95% CI (1.7 to 16.2)), respectively. In multivariate analysis of severe cytopenia risk factors, only year of CAR-T infusion (HR=0.61, 95% CI (0.39 to 0.95), p=0.028) and total number of treatment lines before CAR-T infusion (one or two lines vs three or more, HR=0.41, 95% CI (0.21 to 0.83), p=0.013) had a significant positive association with the incidence of cytopenia. Other factors, such as previous transplantation, disease status at time of CAR-T, patient age and patient sex, had no significant association. Our data provide insight on frequency and clinical relevance of severe cytopenia after CAR T-cell therapy in the European real-world setting. BMJ Publishing Group 2023-04-17 /pmc/articles/PMC10124318/ /pubmed/37072350 http://dx.doi.org/10.1136/jitc-2022-006406 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Immune Cell Therapies and Immune Cell Engineering
Penack, Olaf
Peczynski, Christophe
Koenecke, Christian
Polge, Emmanuelle
Kuhnl, Andrea
Fegueux, Nathalie
Daskalakis, Michael
Kröger, Nicolaus
Dreger, Peter
Besley, Caroline
Schanz, Urs
Bloor, Adrian
Ganser, Arnold
Forcade, Edouard
Corral, Lucia López
Passweg, Jakob R
Novak, Urban
Moiseev, Ivan
Schoemans, Hélène
Basak, Grzegorz W
Chabannon, Christian
Sureda, Anna
Averbuch, Dina
Glass, Bertram
de la Camara, Rafael
Peric, Zinaida
Severe cytopenia after CD19 CAR T-cell therapy: a retrospective study from the EBMT Transplant Complications Working Party
title Severe cytopenia after CD19 CAR T-cell therapy: a retrospective study from the EBMT Transplant Complications Working Party
title_full Severe cytopenia after CD19 CAR T-cell therapy: a retrospective study from the EBMT Transplant Complications Working Party
title_fullStr Severe cytopenia after CD19 CAR T-cell therapy: a retrospective study from the EBMT Transplant Complications Working Party
title_full_unstemmed Severe cytopenia after CD19 CAR T-cell therapy: a retrospective study from the EBMT Transplant Complications Working Party
title_short Severe cytopenia after CD19 CAR T-cell therapy: a retrospective study from the EBMT Transplant Complications Working Party
title_sort severe cytopenia after cd19 car t-cell therapy: a retrospective study from the ebmt transplant complications working party
topic Immune Cell Therapies and Immune Cell Engineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124318/
https://www.ncbi.nlm.nih.gov/pubmed/37072350
http://dx.doi.org/10.1136/jitc-2022-006406
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