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Axicabtagene Ciloleucel: The First FDA-Approved CAR T-Cell Therapy for Relapsed/Refractory Large B-Cell Lymphoma
Axicabtagene ciloleucel (axi-cel) is an anti-CD19 CAR T-cell therapy that has demonstrated efficacy in relapsed and refractory diffuse large B-cell lymphoma (DLBCL) patients who have had suboptimal responses to conventional therapies. The immune activation that confers the efficacy of axi-cel comes...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Harborside Press LLC
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7517758/ https://www.ncbi.nlm.nih.gov/pubmed/33425471 http://dx.doi.org/10.6004/jadpro.2019.10.8.9 |
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author | King, Amber C. Orozco, Jennifer S. |
author_facet | King, Amber C. Orozco, Jennifer S. |
author_sort | King, Amber C. |
collection | PubMed |
description | Axicabtagene ciloleucel (axi-cel) is an anti-CD19 CAR T-cell therapy that has demonstrated efficacy in relapsed and refractory diffuse large B-cell lymphoma (DLBCL) patients who have had suboptimal responses to conventional therapies. The immune activation that confers the efficacy of axi-cel comes at the price of potentially devastating adverse phenomena: cytokine release syndrome and neurotoxicity. This article serves as an overview of axi-cel, including a review of the available clinical evidence, mechanism of action, and management of some of the unique toxicities of axi-cel. |
format | Online Article Text |
id | pubmed-7517758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Harborside Press LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-75177582021-01-07 Axicabtagene Ciloleucel: The First FDA-Approved CAR T-Cell Therapy for Relapsed/Refractory Large B-Cell Lymphoma King, Amber C. Orozco, Jennifer S. J Adv Pract Oncol Prescriber's Corner Axicabtagene ciloleucel (axi-cel) is an anti-CD19 CAR T-cell therapy that has demonstrated efficacy in relapsed and refractory diffuse large B-cell lymphoma (DLBCL) patients who have had suboptimal responses to conventional therapies. The immune activation that confers the efficacy of axi-cel comes at the price of potentially devastating adverse phenomena: cytokine release syndrome and neurotoxicity. This article serves as an overview of axi-cel, including a review of the available clinical evidence, mechanism of action, and management of some of the unique toxicities of axi-cel. Harborside Press LLC 2019 2019-11-01 /pmc/articles/PMC7517758/ /pubmed/33425471 http://dx.doi.org/10.6004/jadpro.2019.10.8.9 Text en © 2019 Harborside™ http://creativecommons.org/licenses/by-nc-nd/3.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial Non-Derivative License, which permits unrestricted non-commercial and non-derivative use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Prescriber's Corner King, Amber C. Orozco, Jennifer S. Axicabtagene Ciloleucel: The First FDA-Approved CAR T-Cell Therapy for Relapsed/Refractory Large B-Cell Lymphoma |
title | Axicabtagene Ciloleucel: The First FDA-Approved CAR T-Cell Therapy for Relapsed/Refractory Large B-Cell Lymphoma |
title_full | Axicabtagene Ciloleucel: The First FDA-Approved CAR T-Cell Therapy for Relapsed/Refractory Large B-Cell Lymphoma |
title_fullStr | Axicabtagene Ciloleucel: The First FDA-Approved CAR T-Cell Therapy for Relapsed/Refractory Large B-Cell Lymphoma |
title_full_unstemmed | Axicabtagene Ciloleucel: The First FDA-Approved CAR T-Cell Therapy for Relapsed/Refractory Large B-Cell Lymphoma |
title_short | Axicabtagene Ciloleucel: The First FDA-Approved CAR T-Cell Therapy for Relapsed/Refractory Large B-Cell Lymphoma |
title_sort | axicabtagene ciloleucel: the first fda-approved car t-cell therapy for relapsed/refractory large b-cell lymphoma |
topic | Prescriber's Corner |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7517758/ https://www.ncbi.nlm.nih.gov/pubmed/33425471 http://dx.doi.org/10.6004/jadpro.2019.10.8.9 |
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