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Venetoclax: evidence to date and clinical potential

The emergence of targeted therapy for patients with hematological diseases has permanently altered the therapeutic landscape. Immunochemotherapy regimes are now more and more being replaced by targeted therapies due to superior efficacy and better safety profiles. However, evolution and selection of...

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Detalles Bibliográficos
Autores principales: Juárez-Salcedo, Luis Miguel, Desai, Viraj, Dalia, Samir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioExcel Publishing Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788387/
https://www.ncbi.nlm.nih.gov/pubmed/31645879
http://dx.doi.org/10.7573/dic.212574
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author Juárez-Salcedo, Luis Miguel
Desai, Viraj
Dalia, Samir
author_facet Juárez-Salcedo, Luis Miguel
Desai, Viraj
Dalia, Samir
author_sort Juárez-Salcedo, Luis Miguel
collection PubMed
description The emergence of targeted therapy for patients with hematological diseases has permanently altered the therapeutic landscape. Immunochemotherapy regimes are now more and more being replaced by targeted therapies due to superior efficacy and better safety profiles. However, evolution and selection of subclones with continuous treatment leads to disease relapse and resistance toward these novel drugs. Venetoclax, the highly selective BCL-2 inhibitor (ABT-199), has an acceptable safety profile. To date, it has been approved for the treatment of first-line and relapsed/refractory chronic lymphocytic leukemia (CLL) and acute myeloid leukemia (AML). However, extension of indications can be expected in monotherapy and in combination regimens with promising outcomes in other hematological diseases. In this article, we describe the mechanism of action that stands behind the efficacy of venetoclax and provide a summary of available results from clinical trials.
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spelling pubmed-67883872019-10-23 Venetoclax: evidence to date and clinical potential Juárez-Salcedo, Luis Miguel Desai, Viraj Dalia, Samir Drugs Context Review The emergence of targeted therapy for patients with hematological diseases has permanently altered the therapeutic landscape. Immunochemotherapy regimes are now more and more being replaced by targeted therapies due to superior efficacy and better safety profiles. However, evolution and selection of subclones with continuous treatment leads to disease relapse and resistance toward these novel drugs. Venetoclax, the highly selective BCL-2 inhibitor (ABT-199), has an acceptable safety profile. To date, it has been approved for the treatment of first-line and relapsed/refractory chronic lymphocytic leukemia (CLL) and acute myeloid leukemia (AML). However, extension of indications can be expected in monotherapy and in combination regimens with promising outcomes in other hematological diseases. In this article, we describe the mechanism of action that stands behind the efficacy of venetoclax and provide a summary of available results from clinical trials. BioExcel Publishing Ltd 2019-10-09 /pmc/articles/PMC6788387/ /pubmed/31645879 http://dx.doi.org/10.7573/dic.212574 Text en Copyright © 2019 Juárez-Salcedo LM, Desai V, Dalia S. Published by Drugs in Context under Creative Commons License Deed CC BY NC ND 4.0 which allows anyone to copy, distribute, and transmit the article provided it is properly attributed in the manner specified below. No commercial use without permission.
spellingShingle Review
Juárez-Salcedo, Luis Miguel
Desai, Viraj
Dalia, Samir
Venetoclax: evidence to date and clinical potential
title Venetoclax: evidence to date and clinical potential
title_full Venetoclax: evidence to date and clinical potential
title_fullStr Venetoclax: evidence to date and clinical potential
title_full_unstemmed Venetoclax: evidence to date and clinical potential
title_short Venetoclax: evidence to date and clinical potential
title_sort venetoclax: evidence to date and clinical potential
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788387/
https://www.ncbi.nlm.nih.gov/pubmed/31645879
http://dx.doi.org/10.7573/dic.212574
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