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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 (...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Hematology 2022
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.
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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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