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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2023
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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. |
format | Online Article Text |
id | pubmed-10124318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
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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