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CAR T-cell immunotherapy of B-cell malignancy: the story so far

Chimeric antigen receptor (CAR) T-cell immunotherapy has achieved unprecedented efficacy in the treatment of chemotherapy-resistant or refractory B-cell malignancies. Promising results from pivotal anti-CD19 CAR T-cell phase II trials have led to landmark approvals of two CD19-specific CAR T-cell pr...

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Detalles Bibliográficos
Autores principales: Halim, Leena, Maher, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257863/
https://www.ncbi.nlm.nih.gov/pubmed/32524070
http://dx.doi.org/10.1177/2515135520927164
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author Halim, Leena
Maher, John
author_facet Halim, Leena
Maher, John
author_sort Halim, Leena
collection PubMed
description Chimeric antigen receptor (CAR) T-cell immunotherapy has achieved unprecedented efficacy in the treatment of chemotherapy-resistant or refractory B-cell malignancies. Promising results from pivotal anti-CD19 CAR T-cell phase II trials have led to landmark approvals of two CD19-specific CAR T-cell products by the United States Food and Drug Administration and European Medicines Agency. However, several issues associated with CAR T-cell treatment remain unresolved, such as the management of severe toxicities and the frequent occurrence of both antigen-positive and antigen-negative relapse. Nonetheless, pre-clinical research is advancing at an unprecedented pace to develop innovative solutions to address these issues. Herein, we summarise recent clinical developments and outcomes of CD19-targeted CAR T-cell immunotherapy and discuss emerging strategies that may further improve the success, safety and broadened applicability of this approach.
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spelling pubmed-72578632020-06-09 CAR T-cell immunotherapy of B-cell malignancy: the story so far Halim, Leena Maher, John Ther Adv Vaccines Immunother Review Chimeric antigen receptor (CAR) T-cell immunotherapy has achieved unprecedented efficacy in the treatment of chemotherapy-resistant or refractory B-cell malignancies. Promising results from pivotal anti-CD19 CAR T-cell phase II trials have led to landmark approvals of two CD19-specific CAR T-cell products by the United States Food and Drug Administration and European Medicines Agency. However, several issues associated with CAR T-cell treatment remain unresolved, such as the management of severe toxicities and the frequent occurrence of both antigen-positive and antigen-negative relapse. Nonetheless, pre-clinical research is advancing at an unprecedented pace to develop innovative solutions to address these issues. Herein, we summarise recent clinical developments and outcomes of CD19-targeted CAR T-cell immunotherapy and discuss emerging strategies that may further improve the success, safety and broadened applicability of this approach. SAGE Publications 2020-05-27 /pmc/articles/PMC7257863/ /pubmed/32524070 http://dx.doi.org/10.1177/2515135520927164 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
Halim, Leena
Maher, John
CAR T-cell immunotherapy of B-cell malignancy: the story so far
title CAR T-cell immunotherapy of B-cell malignancy: the story so far
title_full CAR T-cell immunotherapy of B-cell malignancy: the story so far
title_fullStr CAR T-cell immunotherapy of B-cell malignancy: the story so far
title_full_unstemmed CAR T-cell immunotherapy of B-cell malignancy: the story so far
title_short CAR T-cell immunotherapy of B-cell malignancy: the story so far
title_sort car t-cell immunotherapy of b-cell malignancy: the story so far
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257863/
https://www.ncbi.nlm.nih.gov/pubmed/32524070
http://dx.doi.org/10.1177/2515135520927164
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