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PI3K/Akt/mTOR inhibitors in breast cancer

Activation of the phosphoinositide 3 kinase (PI3K)/Akt/mammalian target of rapamycin (mTOR) pathway is common in breast cancer. There is preclinical data to support inhibition of the pathway, and phase I to III trials involving inhibitors of the pathway have been or are being conducted in solid tumo...

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Autores principales: Lee, Joycelyn JX, Loh, Kiley, Yap, Yoon-Sim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Anti-Cancer Association 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706528/
https://www.ncbi.nlm.nih.gov/pubmed/26779371
http://dx.doi.org/10.7497/j.issn.2095-3941.2015.0089
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author Lee, Joycelyn JX
Loh, Kiley
Yap, Yoon-Sim
author_facet Lee, Joycelyn JX
Loh, Kiley
Yap, Yoon-Sim
author_sort Lee, Joycelyn JX
collection PubMed
description Activation of the phosphoinositide 3 kinase (PI3K)/Akt/mammalian target of rapamycin (mTOR) pathway is common in breast cancer. There is preclinical data to support inhibition of the pathway, and phase I to III trials involving inhibitors of the pathway have been or are being conducted in solid tumors and breast cancer. Everolimus, an mTOR inhibitor, is currently approved for the treatment of hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer. In this review, we summarise the efficacy and toxicity findings from the randomised clinical trials, with simplified guidelines on the management of potential adverse effects. Education of healthcare professionals and patients is critical for safety and compliance. While there is some clinical evidence of activity of mTOR inhibition in HR-positive and HER2-positive breast cancers, the benefits may be more pronounced in selected subsets rather than in the overall population. Further development of predictive biomarkers will be useful in the selection of patients who will benefit from inhibition of the PI3K/Akt/mTOR (PAM) pathway.
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spelling pubmed-47065282016-01-15 PI3K/Akt/mTOR inhibitors in breast cancer Lee, Joycelyn JX Loh, Kiley Yap, Yoon-Sim Cancer Biol Med Review Article Activation of the phosphoinositide 3 kinase (PI3K)/Akt/mammalian target of rapamycin (mTOR) pathway is common in breast cancer. There is preclinical data to support inhibition of the pathway, and phase I to III trials involving inhibitors of the pathway have been or are being conducted in solid tumors and breast cancer. Everolimus, an mTOR inhibitor, is currently approved for the treatment of hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer. In this review, we summarise the efficacy and toxicity findings from the randomised clinical trials, with simplified guidelines on the management of potential adverse effects. Education of healthcare professionals and patients is critical for safety and compliance. While there is some clinical evidence of activity of mTOR inhibition in HR-positive and HER2-positive breast cancers, the benefits may be more pronounced in selected subsets rather than in the overall population. Further development of predictive biomarkers will be useful in the selection of patients who will benefit from inhibition of the PI3K/Akt/mTOR (PAM) pathway. Chinese Anti-Cancer Association 2015-12 /pmc/articles/PMC4706528/ /pubmed/26779371 http://dx.doi.org/10.7497/j.issn.2095-3941.2015.0089 Text en 2015 Cancer Biology & Medicine This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Review Article
Lee, Joycelyn JX
Loh, Kiley
Yap, Yoon-Sim
PI3K/Akt/mTOR inhibitors in breast cancer
title PI3K/Akt/mTOR inhibitors in breast cancer
title_full PI3K/Akt/mTOR inhibitors in breast cancer
title_fullStr PI3K/Akt/mTOR inhibitors in breast cancer
title_full_unstemmed PI3K/Akt/mTOR inhibitors in breast cancer
title_short PI3K/Akt/mTOR inhibitors in breast cancer
title_sort pi3k/akt/mtor inhibitors in breast cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706528/
https://www.ncbi.nlm.nih.gov/pubmed/26779371
http://dx.doi.org/10.7497/j.issn.2095-3941.2015.0089
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