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Therapeutic Advances in Relapsed and Refractory Peripheral T-Cell Lymphoma

SIMPLE SUMMARY: T-cell lymphomas are a rare, heterogeneous family of lymphomas derived from post-thymic T lymphocytes. For patients with relapsed or refractory disease, outcomes are generally poor, with overall survival usually less than one year in the absence of an allogeneic hematopoietic stem ce...

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Autores principales: Stuver, Robert, Moskowitz, Alison J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9913081/
https://www.ncbi.nlm.nih.gov/pubmed/36765544
http://dx.doi.org/10.3390/cancers15030589
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author Stuver, Robert
Moskowitz, Alison J.
author_facet Stuver, Robert
Moskowitz, Alison J.
author_sort Stuver, Robert
collection PubMed
description SIMPLE SUMMARY: T-cell lymphomas are a rare, heterogeneous family of lymphomas derived from post-thymic T lymphocytes. For patients with relapsed or refractory disease, outcomes are generally poor, with overall survival usually less than one year in the absence of an allogeneic hematopoietic stem cell transplantation. The historic approach to relapsed or refractory disease has been the use of non-overlapping combination chemotherapy. However, tremendous progress has been made in understanding the pathogenesis of these diseases, leading to a plethora of novel, biologically rational therapies. In this review, we provide an updated evaluation of therapeutic advances in relapsed and refractory T-cell lymphomas, focusing on approved agents and promising investigational regimens with emerging data within the last five years. We provide a basic framework for the management of disease in this setting. ABSTRACT: Historic outcomes for patients with relapsed or refractory nodal-based T-cell lymphomas are poor, with survival generally measured in months in multiple reports from the late 20th and early 21st century. Until recently, salvage strategies have mostly been borrowed from other aggressive lymphomas. However, dedicated investigations into the pathogenesis of T-cell lymphomas have resulted in an outpouring of therapies that target these diseases in biologically rational strategies. In particular, an evolving appreciation of the multiple complex oncogenic pathways and epigenetic changes that underlie these diseases has led to numerous agents targeting these aberrancies. Moreover, large reports of salvage allogeneic stem cell transplants in T-cell lymphoma have now been published, showing that adaptive immunotherapy is a potentially curative strategy for patients with relapsed or refractory disease. This review highlights therapeutic advances for relapsed or refractory T-cell lymphomas, including cellular therapy and allogeneic stem cell transplant, and provides a framework for management.
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spelling pubmed-99130812023-02-11 Therapeutic Advances in Relapsed and Refractory Peripheral T-Cell Lymphoma Stuver, Robert Moskowitz, Alison J. Cancers (Basel) Review SIMPLE SUMMARY: T-cell lymphomas are a rare, heterogeneous family of lymphomas derived from post-thymic T lymphocytes. For patients with relapsed or refractory disease, outcomes are generally poor, with overall survival usually less than one year in the absence of an allogeneic hematopoietic stem cell transplantation. The historic approach to relapsed or refractory disease has been the use of non-overlapping combination chemotherapy. However, tremendous progress has been made in understanding the pathogenesis of these diseases, leading to a plethora of novel, biologically rational therapies. In this review, we provide an updated evaluation of therapeutic advances in relapsed and refractory T-cell lymphomas, focusing on approved agents and promising investigational regimens with emerging data within the last five years. We provide a basic framework for the management of disease in this setting. ABSTRACT: Historic outcomes for patients with relapsed or refractory nodal-based T-cell lymphomas are poor, with survival generally measured in months in multiple reports from the late 20th and early 21st century. Until recently, salvage strategies have mostly been borrowed from other aggressive lymphomas. However, dedicated investigations into the pathogenesis of T-cell lymphomas have resulted in an outpouring of therapies that target these diseases in biologically rational strategies. In particular, an evolving appreciation of the multiple complex oncogenic pathways and epigenetic changes that underlie these diseases has led to numerous agents targeting these aberrancies. Moreover, large reports of salvage allogeneic stem cell transplants in T-cell lymphoma have now been published, showing that adaptive immunotherapy is a potentially curative strategy for patients with relapsed or refractory disease. This review highlights therapeutic advances for relapsed or refractory T-cell lymphomas, including cellular therapy and allogeneic stem cell transplant, and provides a framework for management. MDPI 2023-01-18 /pmc/articles/PMC9913081/ /pubmed/36765544 http://dx.doi.org/10.3390/cancers15030589 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Stuver, Robert
Moskowitz, Alison J.
Therapeutic Advances in Relapsed and Refractory Peripheral T-Cell Lymphoma
title Therapeutic Advances in Relapsed and Refractory Peripheral T-Cell Lymphoma
title_full Therapeutic Advances in Relapsed and Refractory Peripheral T-Cell Lymphoma
title_fullStr Therapeutic Advances in Relapsed and Refractory Peripheral T-Cell Lymphoma
title_full_unstemmed Therapeutic Advances in Relapsed and Refractory Peripheral T-Cell Lymphoma
title_short Therapeutic Advances in Relapsed and Refractory Peripheral T-Cell Lymphoma
title_sort therapeutic advances in relapsed and refractory peripheral t-cell lymphoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9913081/
https://www.ncbi.nlm.nih.gov/pubmed/36765544
http://dx.doi.org/10.3390/cancers15030589
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