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Romidepsin for the Treatment of Peripheral T-Cell Lymphoma

Peripheral T-cell lymphomas (PTCLs) are a rare, heterogeneous group of T-cell– or natural killer cell–derived non-Hodgkin lymphomas. The majority of patients with PTCL experience an aggressive disease course and poor overall survival. Historically, PTCL has been treated with chemotherapy regimens us...

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Detalles Bibliográficos
Autores principales: Barbarotta, Lisa, Hurley, Kristen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Harborside Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577031/
https://www.ncbi.nlm.nih.gov/pubmed/26413372
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author Barbarotta, Lisa
Hurley, Kristen
author_facet Barbarotta, Lisa
Hurley, Kristen
author_sort Barbarotta, Lisa
collection PubMed
description Peripheral T-cell lymphomas (PTCLs) are a rare, heterogeneous group of T-cell– or natural killer cell–derived non-Hodgkin lymphomas. The majority of patients with PTCL experience an aggressive disease course and poor overall survival. Historically, PTCL has been treated with chemotherapy regimens used to treat B-cell lymphomas; however, a lack of durable responses to frontline therapies and few effective options for salvage treatment have led to the development of newer therapies. Romidepsin is a structurally unique, potent, bicyclic class 1 selective histone deacetylase (HDAC) inhibitor that has demonstrated durable clinical responses in patients with relapsed/refractory PTCL, leading to its approval by the US Food and Drug Administration in 2011 for the treatment of PTCL in patients who have received at least one prior therapy. Here, the authors provide an overview of PTCL, review the role of HDAC inhibitors as anticancer agents, discuss romidepsin use in PTCL, and highlight considerations for advanced practitioners (including the management of side effects).
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spelling pubmed-45770312015-09-25 Romidepsin for the Treatment of Peripheral T-Cell Lymphoma Barbarotta, Lisa Hurley, Kristen J Adv Pract Oncol Review Article Peripheral T-cell lymphomas (PTCLs) are a rare, heterogeneous group of T-cell– or natural killer cell–derived non-Hodgkin lymphomas. The majority of patients with PTCL experience an aggressive disease course and poor overall survival. Historically, PTCL has been treated with chemotherapy regimens used to treat B-cell lymphomas; however, a lack of durable responses to frontline therapies and few effective options for salvage treatment have led to the development of newer therapies. Romidepsin is a structurally unique, potent, bicyclic class 1 selective histone deacetylase (HDAC) inhibitor that has demonstrated durable clinical responses in patients with relapsed/refractory PTCL, leading to its approval by the US Food and Drug Administration in 2011 for the treatment of PTCL in patients who have received at least one prior therapy. Here, the authors provide an overview of PTCL, review the role of HDAC inhibitors as anticancer agents, discuss romidepsin use in PTCL, and highlight considerations for advanced practitioners (including the management of side effects). Harborside Press 2015 2015-01-01 /pmc/articles/PMC4577031/ /pubmed/26413372 Text en Copyright © 2015, Harborside Press http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited and is for non-commercial purposes.
spellingShingle Review Article
Barbarotta, Lisa
Hurley, Kristen
Romidepsin for the Treatment of Peripheral T-Cell Lymphoma
title Romidepsin for the Treatment of Peripheral T-Cell Lymphoma
title_full Romidepsin for the Treatment of Peripheral T-Cell Lymphoma
title_fullStr Romidepsin for the Treatment of Peripheral T-Cell Lymphoma
title_full_unstemmed Romidepsin for the Treatment of Peripheral T-Cell Lymphoma
title_short Romidepsin for the Treatment of Peripheral T-Cell Lymphoma
title_sort romidepsin for the treatment of peripheral t-cell lymphoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577031/
https://www.ncbi.nlm.nih.gov/pubmed/26413372
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