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Chimeric antigen receptor T cell therapies for multiple myeloma

Multiple myeloma (MM) is the second most common hematologic malignancy and remains incurable despite the advent of numerous new drugs such as proteasome inhibitors (PIs), immunomodulatory agents (IMiDs), and monoclonal antibodies. There is an unmet need to develop novel therapies for refractory/rela...

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Autores principales: Wu, Chao, Zhang, Lina, Brockman, Qierra R., Zhan, Fenghuang, Chen, Lijuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873434/
https://www.ncbi.nlm.nih.gov/pubmed/31752943
http://dx.doi.org/10.1186/s13045-019-0823-5
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author Wu, Chao
Zhang, Lina
Brockman, Qierra R.
Zhan, Fenghuang
Chen, Lijuan
author_facet Wu, Chao
Zhang, Lina
Brockman, Qierra R.
Zhan, Fenghuang
Chen, Lijuan
author_sort Wu, Chao
collection PubMed
description Multiple myeloma (MM) is the second most common hematologic malignancy and remains incurable despite the advent of numerous new drugs such as proteasome inhibitors (PIs), immunomodulatory agents (IMiDs), and monoclonal antibodies. There is an unmet need to develop novel therapies for refractory/relapsed MM. In the past few years, chimeric antigen receptor (CAR)-modified T cell therapy for MM has shown promising efficacy in preclinical and clinical studies. Furthermore, the toxicities of CAR-T cell therapy are manageable. This article summarizes recent developments of CAR-T therapy in MM, focusing on promising targets, new technologies, and new research areas. Additionally, a comprehensive overview of antigen selection is presented along with preliminary results and future directions of CAR-T therapy development.
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spelling pubmed-68734342019-12-12 Chimeric antigen receptor T cell therapies for multiple myeloma Wu, Chao Zhang, Lina Brockman, Qierra R. Zhan, Fenghuang Chen, Lijuan J Hematol Oncol Review Multiple myeloma (MM) is the second most common hematologic malignancy and remains incurable despite the advent of numerous new drugs such as proteasome inhibitors (PIs), immunomodulatory agents (IMiDs), and monoclonal antibodies. There is an unmet need to develop novel therapies for refractory/relapsed MM. In the past few years, chimeric antigen receptor (CAR)-modified T cell therapy for MM has shown promising efficacy in preclinical and clinical studies. Furthermore, the toxicities of CAR-T cell therapy are manageable. This article summarizes recent developments of CAR-T therapy in MM, focusing on promising targets, new technologies, and new research areas. Additionally, a comprehensive overview of antigen selection is presented along with preliminary results and future directions of CAR-T therapy development. BioMed Central 2019-11-21 /pmc/articles/PMC6873434/ /pubmed/31752943 http://dx.doi.org/10.1186/s13045-019-0823-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Wu, Chao
Zhang, Lina
Brockman, Qierra R.
Zhan, Fenghuang
Chen, Lijuan
Chimeric antigen receptor T cell therapies for multiple myeloma
title Chimeric antigen receptor T cell therapies for multiple myeloma
title_full Chimeric antigen receptor T cell therapies for multiple myeloma
title_fullStr Chimeric antigen receptor T cell therapies for multiple myeloma
title_full_unstemmed Chimeric antigen receptor T cell therapies for multiple myeloma
title_short Chimeric antigen receptor T cell therapies for multiple myeloma
title_sort chimeric antigen receptor t cell therapies for multiple myeloma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873434/
https://www.ncbi.nlm.nih.gov/pubmed/31752943
http://dx.doi.org/10.1186/s13045-019-0823-5
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