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New indications and platforms for CAR‐T therapy in lymphomas beyond DLBCL

CD19‐directed chimeric antigen receptor T‐cell therapy (CAR‐T) represents a significant advancement for patients with relapsed/refractory large B‐cell lymphoma (LBCL). Long‐term follow‐up confirms durable remissions in nearly half of the patients, a population that was previously estimated to have a...

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Detalles Bibliográficos
Autores principales: Iqbal, Madiha, Savani, Bipin N, Hamadani, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725814/
https://www.ncbi.nlm.nih.gov/pubmed/34988550
http://dx.doi.org/10.1002/jha2.323
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author Iqbal, Madiha
Savani, Bipin N
Hamadani, Mehdi
author_facet Iqbal, Madiha
Savani, Bipin N
Hamadani, Mehdi
author_sort Iqbal, Madiha
collection PubMed
description CD19‐directed chimeric antigen receptor T‐cell therapy (CAR‐T) represents a significant advancement for patients with relapsed/refractory large B‐cell lymphoma (LBCL). Long‐term follow‐up confirms durable remissions in nearly half of the patients, a population that was previously estimated to have a median survival of around 6 months with standard salvage therapy. This initial success of CAR‐T has led to significant expansion across other lymphoma histologies resulting in the recent regulatory approval of CAR‐T in mantle cell lymphoma and follicular lymphoma. Additionally, multiple novel platforms of CAR‐T therapy are under development to improve efficacy and limit toxicity such dual antigen targeting, allogeneic and natural killer CARs. In this review, we focus on the new indications of CAR‐T in lymphomas beyond LBCL as well as emerging platforms of CAR‐T therapy.
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spelling pubmed-87258142022-01-04 New indications and platforms for CAR‐T therapy in lymphomas beyond DLBCL Iqbal, Madiha Savani, Bipin N Hamadani, Mehdi EJHaem Reviews CD19‐directed chimeric antigen receptor T‐cell therapy (CAR‐T) represents a significant advancement for patients with relapsed/refractory large B‐cell lymphoma (LBCL). Long‐term follow‐up confirms durable remissions in nearly half of the patients, a population that was previously estimated to have a median survival of around 6 months with standard salvage therapy. This initial success of CAR‐T has led to significant expansion across other lymphoma histologies resulting in the recent regulatory approval of CAR‐T in mantle cell lymphoma and follicular lymphoma. Additionally, multiple novel platforms of CAR‐T therapy are under development to improve efficacy and limit toxicity such dual antigen targeting, allogeneic and natural killer CARs. In this review, we focus on the new indications of CAR‐T in lymphomas beyond LBCL as well as emerging platforms of CAR‐T therapy. John Wiley and Sons Inc. 2021-11-23 /pmc/articles/PMC8725814/ /pubmed/34988550 http://dx.doi.org/10.1002/jha2.323 Text en © 2021 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Iqbal, Madiha
Savani, Bipin N
Hamadani, Mehdi
New indications and platforms for CAR‐T therapy in lymphomas beyond DLBCL
title New indications and platforms for CAR‐T therapy in lymphomas beyond DLBCL
title_full New indications and platforms for CAR‐T therapy in lymphomas beyond DLBCL
title_fullStr New indications and platforms for CAR‐T therapy in lymphomas beyond DLBCL
title_full_unstemmed New indications and platforms for CAR‐T therapy in lymphomas beyond DLBCL
title_short New indications and platforms for CAR‐T therapy in lymphomas beyond DLBCL
title_sort new indications and platforms for car‐t therapy in lymphomas beyond dlbcl
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725814/
https://www.ncbi.nlm.nih.gov/pubmed/34988550
http://dx.doi.org/10.1002/jha2.323
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