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Profile of belinostat for the treatment of relapsed or refractory peripheral T-cell lymphoma

The peripheral T-cell lymphomas are a rare and heterogeneous group of mature T-cell lymphomas with limited available therapies. The outcome of frontline chemotherapy regimens has been disappointing, with a long-term survival of only 20%–30%. There is an urgent need to optimize induction therapy by i...

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Autores principales: Bodiford, Andrew, Bodge, Megan, Talbott, Mahsa S, Reddy, Nishitha M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216035/
https://www.ncbi.nlm.nih.gov/pubmed/25368524
http://dx.doi.org/10.2147/OTT.S59269
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author Bodiford, Andrew
Bodge, Megan
Talbott, Mahsa S
Reddy, Nishitha M
author_facet Bodiford, Andrew
Bodge, Megan
Talbott, Mahsa S
Reddy, Nishitha M
author_sort Bodiford, Andrew
collection PubMed
description The peripheral T-cell lymphomas are a rare and heterogeneous group of mature T-cell lymphomas with limited available therapies. The outcome of frontline chemotherapy regimens has been disappointing, with a long-term survival of only 20%–30%. There is an urgent need to optimize induction therapy by incorporating novel agents that target the dysregulated pathways. Histone deacetylase inhibitors that induce acetylation of histones and enhance apoptosis have shown promising activity. In this article, we summarize the role of histone deacetylase inhibitors and specifically discuss pharmacokinetics, efficacy, and toxicity of the recently US Food and Drug Administration-approved agent belinostat for its use in patients with relapsed/refractory peripheral T-cell lymphoma.
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spelling pubmed-42160352014-11-03 Profile of belinostat for the treatment of relapsed or refractory peripheral T-cell lymphoma Bodiford, Andrew Bodge, Megan Talbott, Mahsa S Reddy, Nishitha M Onco Targets Ther Review The peripheral T-cell lymphomas are a rare and heterogeneous group of mature T-cell lymphomas with limited available therapies. The outcome of frontline chemotherapy regimens has been disappointing, with a long-term survival of only 20%–30%. There is an urgent need to optimize induction therapy by incorporating novel agents that target the dysregulated pathways. Histone deacetylase inhibitors that induce acetylation of histones and enhance apoptosis have shown promising activity. In this article, we summarize the role of histone deacetylase inhibitors and specifically discuss pharmacokinetics, efficacy, and toxicity of the recently US Food and Drug Administration-approved agent belinostat for its use in patients with relapsed/refractory peripheral T-cell lymphoma. Dove Medical Press 2014-10-24 /pmc/articles/PMC4216035/ /pubmed/25368524 http://dx.doi.org/10.2147/OTT.S59269 Text en © 2014 Bodiford et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Bodiford, Andrew
Bodge, Megan
Talbott, Mahsa S
Reddy, Nishitha M
Profile of belinostat for the treatment of relapsed or refractory peripheral T-cell lymphoma
title Profile of belinostat for the treatment of relapsed or refractory peripheral T-cell lymphoma
title_full Profile of belinostat for the treatment of relapsed or refractory peripheral T-cell lymphoma
title_fullStr Profile of belinostat for the treatment of relapsed or refractory peripheral T-cell lymphoma
title_full_unstemmed Profile of belinostat for the treatment of relapsed or refractory peripheral T-cell lymphoma
title_short Profile of belinostat for the treatment of relapsed or refractory peripheral T-cell lymphoma
title_sort profile of belinostat for the treatment of relapsed or refractory peripheral t-cell lymphoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216035/
https://www.ncbi.nlm.nih.gov/pubmed/25368524
http://dx.doi.org/10.2147/OTT.S59269
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