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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-8085238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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