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Hematopoietic stem cell boost for persistent neutropenia after CAR T-cell therapy: a GLA/DRST study
Hematotoxicity after chimeric antigen receptor (CAR) T-cell therapy is associated with infection and death but management remains unclear. We report results of 31 patients receiving hematopoietic stem cell boost (HSCB; 30 autologous, 1 allogeneic) for either sustained severe neutropenia of grade 4 (...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society of Hematology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984300/ https://www.ncbi.nlm.nih.gov/pubmed/35696759 http://dx.doi.org/10.1182/bloodadvances.2022008042 |
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author | Gagelmann, Nico Wulf, Gerald Georg Duell, Johannes Glass, Bertram van Heteren, Pearl von Tresckow, Bastian Fischer, Monika Penack, Olaf Ayuk, Francis Einsele, Herrmann Holtick, Udo Thomson, Julia Dreger, Peter Kröger, Nicolaus |
author_facet | Gagelmann, Nico Wulf, Gerald Georg Duell, Johannes Glass, Bertram van Heteren, Pearl von Tresckow, Bastian Fischer, Monika Penack, Olaf Ayuk, Francis Einsele, Herrmann Holtick, Udo Thomson, Julia Dreger, Peter Kröger, Nicolaus |
author_sort | Gagelmann, Nico |
collection | PubMed |
description | Hematotoxicity after chimeric antigen receptor (CAR) T-cell therapy is associated with infection and death but management remains unclear. We report results of 31 patients receiving hematopoietic stem cell boost (HSCB; 30 autologous, 1 allogeneic) for either sustained severe neutropenia of grade 4 (<0.5 × 10(9)/L), sustained moderate neutropenia (≤1.5 × 10(9)/L) and high risk of infection, or neutrophil count ≤2.0 × 10(9)/L and active infection. Median time from CAR T-cell therapy to HSCB was 43 days and median absolute neutrophil count at time of HSCB was 0.2. Median duration of neutropenia before HSCB was 38 days (range, 7-151). Overall neutrophil response rate (recovery or improvement) was observed in 26 patients (84%) within a median of 9 days (95% confidence interval, 7-14). Time to response was significantly associated with the duration of prior neutropenia (P = .007). All nonresponders died within the first year after HSCB. One-year overall survival for all patients was 59% and significantly different for neutropenia (≤38 days; 85%) vs neutropenia >38 days before HSCB (44%; P = .029). In conclusion, early or prophylactic HSCB showed quick response and improved outcomes for sustained moderate to severe neutropenia after CAR-T. |
format | Online Article Text |
id | pubmed-9984300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-99843002023-03-05 Hematopoietic stem cell boost for persistent neutropenia after CAR T-cell therapy: a GLA/DRST study Gagelmann, Nico Wulf, Gerald Georg Duell, Johannes Glass, Bertram van Heteren, Pearl von Tresckow, Bastian Fischer, Monika Penack, Olaf Ayuk, Francis Einsele, Herrmann Holtick, Udo Thomson, Julia Dreger, Peter Kröger, Nicolaus Blood Adv Stimulus Report Hematotoxicity after chimeric antigen receptor (CAR) T-cell therapy is associated with infection and death but management remains unclear. We report results of 31 patients receiving hematopoietic stem cell boost (HSCB; 30 autologous, 1 allogeneic) for either sustained severe neutropenia of grade 4 (<0.5 × 10(9)/L), sustained moderate neutropenia (≤1.5 × 10(9)/L) and high risk of infection, or neutrophil count ≤2.0 × 10(9)/L and active infection. Median time from CAR T-cell therapy to HSCB was 43 days and median absolute neutrophil count at time of HSCB was 0.2. Median duration of neutropenia before HSCB was 38 days (range, 7-151). Overall neutrophil response rate (recovery or improvement) was observed in 26 patients (84%) within a median of 9 days (95% confidence interval, 7-14). Time to response was significantly associated with the duration of prior neutropenia (P = .007). All nonresponders died within the first year after HSCB. One-year overall survival for all patients was 59% and significantly different for neutropenia (≤38 days; 85%) vs neutropenia >38 days before HSCB (44%; P = .029). In conclusion, early or prophylactic HSCB showed quick response and improved outcomes for sustained moderate to severe neutropenia after CAR-T. The American Society of Hematology 2022-06-15 /pmc/articles/PMC9984300/ /pubmed/35696759 http://dx.doi.org/10.1182/bloodadvances.2022008042 Text en © 2023 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Stimulus Report Gagelmann, Nico Wulf, Gerald Georg Duell, Johannes Glass, Bertram van Heteren, Pearl von Tresckow, Bastian Fischer, Monika Penack, Olaf Ayuk, Francis Einsele, Herrmann Holtick, Udo Thomson, Julia Dreger, Peter Kröger, Nicolaus Hematopoietic stem cell boost for persistent neutropenia after CAR T-cell therapy: a GLA/DRST study |
title | Hematopoietic stem cell boost for persistent neutropenia after CAR T-cell therapy: a GLA/DRST study |
title_full | Hematopoietic stem cell boost for persistent neutropenia after CAR T-cell therapy: a GLA/DRST study |
title_fullStr | Hematopoietic stem cell boost for persistent neutropenia after CAR T-cell therapy: a GLA/DRST study |
title_full_unstemmed | Hematopoietic stem cell boost for persistent neutropenia after CAR T-cell therapy: a GLA/DRST study |
title_short | Hematopoietic stem cell boost for persistent neutropenia after CAR T-cell therapy: a GLA/DRST study |
title_sort | hematopoietic stem cell boost for persistent neutropenia after car t-cell therapy: a gla/drst study |
topic | Stimulus Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984300/ https://www.ncbi.nlm.nih.gov/pubmed/35696759 http://dx.doi.org/10.1182/bloodadvances.2022008042 |
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