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Use of CAR T-cell for acute lymphoblastic leukemia (ALL) treatment: a review study
Acute lymphoblastic leukemia (ALL) is a cancer-specific lymphoid cell. Induction and consolidation chemotherapy alone or in combination with different therapeutic approaches remain the main treatment. Although complete or partial remission of the disease can be achieved, the risk of relapse or refra...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395272/ https://www.ncbi.nlm.nih.gov/pubmed/34987176 http://dx.doi.org/10.1038/s41417-021-00418-1 |
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author | Sheykhhasan, Mohsen Manoochehri, Hamed Dama, Paola |
author_facet | Sheykhhasan, Mohsen Manoochehri, Hamed Dama, Paola |
author_sort | Sheykhhasan, Mohsen |
collection | PubMed |
description | Acute lymphoblastic leukemia (ALL) is a cancer-specific lymphoid cell. Induction and consolidation chemotherapy alone or in combination with different therapeutic approaches remain the main treatment. Although complete or partial remission of the disease can be achieved, the risk of relapse or refractory leukemia is still high. More effective and safe therapy options are yet unmet needs. In recent years’ new therapeutic approaches have been widely used. Hematopoietic Stem Cell Transplantation (HSCT) presents significant limitations and the outcome of the consolidation treatment is patient dependent. Side effects such as Graft versus Host Disease (GvHD) in allogeneic hematopoietic stem cell transplantation are extremely common, therefore, using alternative methods to address these challenges for treatment seems crucial. In the last decade, T cells genetically engineered with Chimeric Antigen Receptor (CAR) treatment for the ALL are largely studied and represent the new era of strategy. According to the Phase I/II clinical trials, this technology results seem very promising and can be used in the next future as an effective and safe treatment for ALL treatment. In this review different generations, challenges, and clinical studies related to chimeric antigen receptor (CAR) T-cells for ALL treatment are discussed. |
format | Online Article Text |
id | pubmed-9395272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-93952722022-08-24 Use of CAR T-cell for acute lymphoblastic leukemia (ALL) treatment: a review study Sheykhhasan, Mohsen Manoochehri, Hamed Dama, Paola Cancer Gene Ther Review Article Acute lymphoblastic leukemia (ALL) is a cancer-specific lymphoid cell. Induction and consolidation chemotherapy alone or in combination with different therapeutic approaches remain the main treatment. Although complete or partial remission of the disease can be achieved, the risk of relapse or refractory leukemia is still high. More effective and safe therapy options are yet unmet needs. In recent years’ new therapeutic approaches have been widely used. Hematopoietic Stem Cell Transplantation (HSCT) presents significant limitations and the outcome of the consolidation treatment is patient dependent. Side effects such as Graft versus Host Disease (GvHD) in allogeneic hematopoietic stem cell transplantation are extremely common, therefore, using alternative methods to address these challenges for treatment seems crucial. In the last decade, T cells genetically engineered with Chimeric Antigen Receptor (CAR) treatment for the ALL are largely studied and represent the new era of strategy. According to the Phase I/II clinical trials, this technology results seem very promising and can be used in the next future as an effective and safe treatment for ALL treatment. In this review different generations, challenges, and clinical studies related to chimeric antigen receptor (CAR) T-cells for ALL treatment are discussed. Nature Publishing Group US 2022-01-05 2022 /pmc/articles/PMC9395272/ /pubmed/34987176 http://dx.doi.org/10.1038/s41417-021-00418-1 Text en © Crown 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 Sheykhhasan, Mohsen Manoochehri, Hamed Dama, Paola Use of CAR T-cell for acute lymphoblastic leukemia (ALL) treatment: a review study |
title | Use of CAR T-cell for acute lymphoblastic leukemia (ALL) treatment: a review study |
title_full | Use of CAR T-cell for acute lymphoblastic leukemia (ALL) treatment: a review study |
title_fullStr | Use of CAR T-cell for acute lymphoblastic leukemia (ALL) treatment: a review study |
title_full_unstemmed | Use of CAR T-cell for acute lymphoblastic leukemia (ALL) treatment: a review study |
title_short | Use of CAR T-cell for acute lymphoblastic leukemia (ALL) treatment: a review study |
title_sort | use of car t-cell for acute lymphoblastic leukemia (all) treatment: a review study |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395272/ https://www.ncbi.nlm.nih.gov/pubmed/34987176 http://dx.doi.org/10.1038/s41417-021-00418-1 |
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