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Perspectives for the Use of CAR-T Cells for the Treatment of Multiple Myeloma
During recent years considerable progress has been made in the treatment of multiple myeloma. However, despite the current improvements in the prognosis of this malignancy, it always ends with relapse, and therefore new therapy approaches for destroying resistant cancer cells are needed. Presently,...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943463/ https://www.ncbi.nlm.nih.gov/pubmed/33717171 http://dx.doi.org/10.3389/fimmu.2021.632937 |
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author | Jasiński, Marcin Basak, Grzegorz W. Jedrzejczak, Wiesław W. |
author_facet | Jasiński, Marcin Basak, Grzegorz W. Jedrzejczak, Wiesław W. |
author_sort | Jasiński, Marcin |
collection | PubMed |
description | During recent years considerable progress has been made in the treatment of multiple myeloma. However, despite the current improvements in the prognosis of this malignancy, it always ends with relapse, and therefore new therapy approaches for destroying resistant cancer cells are needed. Presently, there is great hope being placed in the use of immunotherapy against refractory/relapsed multiple myeloma which is unresponsive to any other currently known drugs. The most promising one is CAR-T cell therapy which has already shown tremendous success in treating other malignancies such as acute lymphoblastic leukaemia (ALL) and could potentially be administered to multiple myeloma patients. CAR-T cells equipped with receptors against BCMA (B-cell maturation antigen), which is a surface antigen that is highly expressed on malignant cells, are now of great interest in this field with significant results in clinical trials. Furthermore, CAR-T cells with other receptors and combinations of different strategies are being intensively studied. However, even with CAR-T cell therapy, the majority of patients eventually relapse, which is the greatest limitation of this therapy. Serious adverse events such as cytokine release syndrome or neurotoxicity should also be considered as possible side effects of CAR-T cell therapy. Here, we discuss the results of CAR-T cell therapy in the treatment of multiple myeloma, where we describe its main advantages and disadvantages. Additionally, we also describe the current results that have been obtained on using combinations of CAR-T cell therapies with other drugs for the treatment of multiple myeloma. |
format | Online Article Text |
id | pubmed-7943463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79434632021-03-11 Perspectives for the Use of CAR-T Cells for the Treatment of Multiple Myeloma Jasiński, Marcin Basak, Grzegorz W. Jedrzejczak, Wiesław W. Front Immunol Immunology During recent years considerable progress has been made in the treatment of multiple myeloma. However, despite the current improvements in the prognosis of this malignancy, it always ends with relapse, and therefore new therapy approaches for destroying resistant cancer cells are needed. Presently, there is great hope being placed in the use of immunotherapy against refractory/relapsed multiple myeloma which is unresponsive to any other currently known drugs. The most promising one is CAR-T cell therapy which has already shown tremendous success in treating other malignancies such as acute lymphoblastic leukaemia (ALL) and could potentially be administered to multiple myeloma patients. CAR-T cells equipped with receptors against BCMA (B-cell maturation antigen), which is a surface antigen that is highly expressed on malignant cells, are now of great interest in this field with significant results in clinical trials. Furthermore, CAR-T cells with other receptors and combinations of different strategies are being intensively studied. However, even with CAR-T cell therapy, the majority of patients eventually relapse, which is the greatest limitation of this therapy. Serious adverse events such as cytokine release syndrome or neurotoxicity should also be considered as possible side effects of CAR-T cell therapy. Here, we discuss the results of CAR-T cell therapy in the treatment of multiple myeloma, where we describe its main advantages and disadvantages. Additionally, we also describe the current results that have been obtained on using combinations of CAR-T cell therapies with other drugs for the treatment of multiple myeloma. Frontiers Media S.A. 2021-02-24 /pmc/articles/PMC7943463/ /pubmed/33717171 http://dx.doi.org/10.3389/fimmu.2021.632937 Text en Copyright © 2021 Jasiński, Basak and Jedrzejczak http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Jasiński, Marcin Basak, Grzegorz W. Jedrzejczak, Wiesław W. Perspectives for the Use of CAR-T Cells for the Treatment of Multiple Myeloma |
title | Perspectives for the Use of CAR-T Cells for the Treatment of Multiple Myeloma |
title_full | Perspectives for the Use of CAR-T Cells for the Treatment of Multiple Myeloma |
title_fullStr | Perspectives for the Use of CAR-T Cells for the Treatment of Multiple Myeloma |
title_full_unstemmed | Perspectives for the Use of CAR-T Cells for the Treatment of Multiple Myeloma |
title_short | Perspectives for the Use of CAR-T Cells for the Treatment of Multiple Myeloma |
title_sort | perspectives for the use of car-t cells for the treatment of multiple myeloma |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943463/ https://www.ncbi.nlm.nih.gov/pubmed/33717171 http://dx.doi.org/10.3389/fimmu.2021.632937 |
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