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Profile of abemaciclib and its potential in the treatment of breast cancer

Hormone-receptor-positive breast cancer is the most common subtype of breast cancer among patients with both early-stage and metastatic disease. Recent advances in the understanding of its pathophysiology have led to the discovery and utilization of targeted inhibitors to cyclin-dependent kinases 4...

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Autores principales: Martin, James M, Goldstein, Lori J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120573/
https://www.ncbi.nlm.nih.gov/pubmed/30214230
http://dx.doi.org/10.2147/OTT.S149245
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author Martin, James M
Goldstein, Lori J
author_facet Martin, James M
Goldstein, Lori J
author_sort Martin, James M
collection PubMed
description Hormone-receptor-positive breast cancer is the most common subtype of breast cancer among patients with both early-stage and metastatic disease. Recent advances in the understanding of its pathophysiology have led to the discovery and utilization of targeted inhibitors to cyclin-dependent kinases 4 and 6 (CDK4/6). There are currently three available CDK4/6 inhibitors available for use in USA: palbociclib, ribociclib, and abemaciclib. Their oral administration and tolerable toxicities make this class of agents appealing to both patients and health care providers. Abemaciclib, the most recently approved CDK4/6 inhibitor, has unique pharmacologic properties and potential toxicities. This review highlights the current understanding of abemaciclib and discusses its current and future roles in the treatment of breast cancer.
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spelling pubmed-61205732018-09-13 Profile of abemaciclib and its potential in the treatment of breast cancer Martin, James M Goldstein, Lori J Onco Targets Ther Review Hormone-receptor-positive breast cancer is the most common subtype of breast cancer among patients with both early-stage and metastatic disease. Recent advances in the understanding of its pathophysiology have led to the discovery and utilization of targeted inhibitors to cyclin-dependent kinases 4 and 6 (CDK4/6). There are currently three available CDK4/6 inhibitors available for use in USA: palbociclib, ribociclib, and abemaciclib. Their oral administration and tolerable toxicities make this class of agents appealing to both patients and health care providers. Abemaciclib, the most recently approved CDK4/6 inhibitor, has unique pharmacologic properties and potential toxicities. This review highlights the current understanding of abemaciclib and discusses its current and future roles in the treatment of breast cancer. Dove Medical Press 2018-08-29 /pmc/articles/PMC6120573/ /pubmed/30214230 http://dx.doi.org/10.2147/OTT.S149245 Text en © 2018 Martin and Goldstein. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. 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
Martin, James M
Goldstein, Lori J
Profile of abemaciclib and its potential in the treatment of breast cancer
title Profile of abemaciclib and its potential in the treatment of breast cancer
title_full Profile of abemaciclib and its potential in the treatment of breast cancer
title_fullStr Profile of abemaciclib and its potential in the treatment of breast cancer
title_full_unstemmed Profile of abemaciclib and its potential in the treatment of breast cancer
title_short Profile of abemaciclib and its potential in the treatment of breast cancer
title_sort profile of abemaciclib and its potential in the treatment of breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120573/
https://www.ncbi.nlm.nih.gov/pubmed/30214230
http://dx.doi.org/10.2147/OTT.S149245
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