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Chimeric antigen receptor (CAR) T-cell treatment for mantle cell lymphoma (MCL)
Mantle cell lymphoma (MCL) is a rare B-cell malignancy that remains challenging to treat with high rates of relapse. Frontline strategies range from intensive chemotherapy followed by consolidation with autologous stem cell transplant (ASCT), to less-intensive therapies including combination regimen...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8882938/ https://www.ncbi.nlm.nih.gov/pubmed/35237395 http://dx.doi.org/10.1177/20406207221080738 |
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author | Tbakhi, Bushra Reagan, Patrick M. |
author_facet | Tbakhi, Bushra Reagan, Patrick M. |
author_sort | Tbakhi, Bushra |
collection | PubMed |
description | Mantle cell lymphoma (MCL) is a rare B-cell malignancy that remains challenging to treat with high rates of relapse. Frontline strategies range from intensive chemotherapy followed by consolidation with autologous stem cell transplant (ASCT), to less-intensive therapies including combination regimens. The treatment landscape for relapsed patients includes Bruton tyrosine kinase (BTK) inhibitors among other targeted treatments. Novel agents such as the selective BCL2 inhibitor venetoclax showed high response rates when used as monotherapy for refractory relapsed MCL. The rituximab, bendamustine, and cytarabine (R-BAC) regimen, while response rates were high, were not durable. Chimeric antigen receptor (CAR) T-cell products targeting CD19 have been efficacious in relapsed and refractory MCL patients. Brexucabtagene autoleucel (brexu-cel, formerly KTE-X19) was approved by US Food and Drug Administration (FDA) in July, 2020, for treatment of refractory and relapsed MCL. This article provides an overview for the available management strategies for relapsed MCL and examines the role of CAR T-cell in the current and future treatment of MCL. |
format | Online Article Text |
id | pubmed-8882938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-88829382022-03-01 Chimeric antigen receptor (CAR) T-cell treatment for mantle cell lymphoma (MCL) Tbakhi, Bushra Reagan, Patrick M. Ther Adv Hematol Review Mantle cell lymphoma (MCL) is a rare B-cell malignancy that remains challenging to treat with high rates of relapse. Frontline strategies range from intensive chemotherapy followed by consolidation with autologous stem cell transplant (ASCT), to less-intensive therapies including combination regimens. The treatment landscape for relapsed patients includes Bruton tyrosine kinase (BTK) inhibitors among other targeted treatments. Novel agents such as the selective BCL2 inhibitor venetoclax showed high response rates when used as monotherapy for refractory relapsed MCL. The rituximab, bendamustine, and cytarabine (R-BAC) regimen, while response rates were high, were not durable. Chimeric antigen receptor (CAR) T-cell products targeting CD19 have been efficacious in relapsed and refractory MCL patients. Brexucabtagene autoleucel (brexu-cel, formerly KTE-X19) was approved by US Food and Drug Administration (FDA) in July, 2020, for treatment of refractory and relapsed MCL. This article provides an overview for the available management strategies for relapsed MCL and examines the role of CAR T-cell in the current and future treatment of MCL. SAGE Publications 2022-02-26 /pmc/articles/PMC8882938/ /pubmed/35237395 http://dx.doi.org/10.1177/20406207221080738 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Tbakhi, Bushra Reagan, Patrick M. Chimeric antigen receptor (CAR) T-cell treatment for mantle cell lymphoma (MCL) |
title | Chimeric antigen receptor (CAR) T-cell treatment for mantle cell
lymphoma (MCL) |
title_full | Chimeric antigen receptor (CAR) T-cell treatment for mantle cell
lymphoma (MCL) |
title_fullStr | Chimeric antigen receptor (CAR) T-cell treatment for mantle cell
lymphoma (MCL) |
title_full_unstemmed | Chimeric antigen receptor (CAR) T-cell treatment for mantle cell
lymphoma (MCL) |
title_short | Chimeric antigen receptor (CAR) T-cell treatment for mantle cell
lymphoma (MCL) |
title_sort | chimeric antigen receptor (car) t-cell treatment for mantle cell
lymphoma (mcl) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8882938/ https://www.ncbi.nlm.nih.gov/pubmed/35237395 http://dx.doi.org/10.1177/20406207221080738 |
work_keys_str_mv | AT tbakhibushra chimericantigenreceptorcartcelltreatmentformantlecelllymphomamcl AT reaganpatrickm chimericantigenreceptorcartcelltreatmentformantlecelllymphomamcl |