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CAR T-cell therapy in multiple myeloma: more room for improvement

The emergence of various novel therapies over the last decade has changed the therapeutic landscape for multiple myeloma. While the clinical outcomes have improved significantly, the disease remains incurable, typically in patients with relapsed and refractory disease. Chimeric antigen receptor (CAR...

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Detalles Bibliográficos
Autores principales: Teoh, Phaik Ju, Chng, Wee Joo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085238/
https://www.ncbi.nlm.nih.gov/pubmed/33927192
http://dx.doi.org/10.1038/s41408-021-00469-5
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author Teoh, Phaik Ju
Chng, Wee Joo
author_facet Teoh, Phaik Ju
Chng, Wee Joo
author_sort Teoh, Phaik Ju
collection PubMed
description The emergence of various novel therapies over the last decade has changed the therapeutic landscape for multiple myeloma. While the clinical outcomes have improved significantly, the disease remains incurable, typically in patients with relapsed and refractory disease. Chimeric antigen receptor (CAR) T-cell therapies have achieved remarkable clinical success in B-cell malignancies. This scope of research has more recently been extended to the field of myeloma. While B-cell maturation antigen (BCMA) is currently the most well-studied CAR T antigen target in this disease, many other antigens are also undergoing intensive investigations. Some studies have shown encouraging results, whereas some others have demonstrated unfavorable results due to reasons such as toxicity and lack of clinical efficacy. Herein, we provide an overview of CAR T-cell therapies in myeloma, highlighted what has been achieved over the past decade, including the latest updates from ASH 2020 and discussed some of the challenges faced. Considering the current hits and misses of CAR T therapies, we provide a comprehensive analysis on the current manufacturing technologies, and deliberate on the future of CAR T-cell domain in MM.
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spelling pubmed-80852382021-05-05 CAR T-cell therapy in multiple myeloma: more room for improvement Teoh, Phaik Ju Chng, Wee Joo Blood Cancer J Review Article The emergence of various novel therapies over the last decade has changed the therapeutic landscape for multiple myeloma. While the clinical outcomes have improved significantly, the disease remains incurable, typically in patients with relapsed and refractory disease. Chimeric antigen receptor (CAR) T-cell therapies have achieved remarkable clinical success in B-cell malignancies. This scope of research has more recently been extended to the field of myeloma. While B-cell maturation antigen (BCMA) is currently the most well-studied CAR T antigen target in this disease, many other antigens are also undergoing intensive investigations. Some studies have shown encouraging results, whereas some others have demonstrated unfavorable results due to reasons such as toxicity and lack of clinical efficacy. Herein, we provide an overview of CAR T-cell therapies in myeloma, highlighted what has been achieved over the past decade, including the latest updates from ASH 2020 and discussed some of the challenges faced. Considering the current hits and misses of CAR T therapies, we provide a comprehensive analysis on the current manufacturing technologies, and deliberate on the future of CAR T-cell domain in MM. Nature Publishing Group UK 2021-04-29 /pmc/articles/PMC8085238/ /pubmed/33927192 http://dx.doi.org/10.1038/s41408-021-00469-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Teoh, Phaik Ju
Chng, Wee Joo
CAR T-cell therapy in multiple myeloma: more room for improvement
title CAR T-cell therapy in multiple myeloma: more room for improvement
title_full CAR T-cell therapy in multiple myeloma: more room for improvement
title_fullStr CAR T-cell therapy in multiple myeloma: more room for improvement
title_full_unstemmed CAR T-cell therapy in multiple myeloma: more room for improvement
title_short CAR T-cell therapy in multiple myeloma: more room for improvement
title_sort car t-cell therapy in multiple myeloma: more room for improvement
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085238/
https://www.ncbi.nlm.nih.gov/pubmed/33927192
http://dx.doi.org/10.1038/s41408-021-00469-5
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