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Influence of Androgen Receptor Expression on the Survival Outcomes in Breast Cancer: A Meta-Analysis

PURPOSE: Despite the fact that the androgen receptor (AR) is known to be involved in the pathogenesis of breast cancer, its prognostic effect remains controversial. In this meta-analysis, we explored AR expression and its impact on survival outcomes in breast cancer. METHODS: We searched PubMed, EMB...

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Autores principales: Kim, Yoonseok, Jae, Eunae, Yoon, Myunghee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Breast Cancer Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490262/
https://www.ncbi.nlm.nih.gov/pubmed/26155289
http://dx.doi.org/10.4048/jbc.2015.18.2.134
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author Kim, Yoonseok
Jae, Eunae
Yoon, Myunghee
author_facet Kim, Yoonseok
Jae, Eunae
Yoon, Myunghee
author_sort Kim, Yoonseok
collection PubMed
description PURPOSE: Despite the fact that the androgen receptor (AR) is known to be involved in the pathogenesis of breast cancer, its prognostic effect remains controversial. In this meta-analysis, we explored AR expression and its impact on survival outcomes in breast cancer. METHODS: We searched PubMed, EMBASE, Cochrane Library, ScienceDirect, SpringerLink, and Ovid databases and references of articles to identify studies reporting data until December 2013. Disease-free survival (DFS) and overall survival (OS) were analyzed by extracting the number of patients with recurrence and survival according to AR expression. RESULTS: There were 16 articles that met the criteria for inclusion in our meta-analysis. DFS and OS were significantly longer in patients with AR expression compared with patients without AR expression (odds ratio [OR], 0.60; 95% confidence interval [CI], 0.40-0.90; OR, 0.53; 95% CI, 0.38-0.73, respectively). In addition, hormone receptor (HR) positive patients had a longer DFS when AR was also expressed (OR, 0.63; 95% CI, 0.41-0.98). For patients with triple negative breast cancer (TNBC), AR expression was also associated with longer DFS and OS (OR, 0.44, 95% CI, 0.26-0.75; OR, 0.26, 95% CI, 0.12-0.55, respectively). Furthermore, AR expression was associated with a longer DFS and OS in women (OR, 0.42, 95% CI, 0.27-0.64; OR, 0.47, 95% CI, 0.38-0.59, respectively). However, in men, AR expression was associated with a worse DFS (OR, 6.00; 95% CI, 1.46-24.73). CONCLUSION: Expression of AR in breast cancer might be associated with better survival outcomes, especially in patients with HR-positive tumors and TNBC, and women. Based on this meta-analysis, we propose that AR expression might be related to prognostic features and contribute to clinical outcomes.
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spelling pubmed-44902622015-07-07 Influence of Androgen Receptor Expression on the Survival Outcomes in Breast Cancer: A Meta-Analysis Kim, Yoonseok Jae, Eunae Yoon, Myunghee J Breast Cancer Original Article PURPOSE: Despite the fact that the androgen receptor (AR) is known to be involved in the pathogenesis of breast cancer, its prognostic effect remains controversial. In this meta-analysis, we explored AR expression and its impact on survival outcomes in breast cancer. METHODS: We searched PubMed, EMBASE, Cochrane Library, ScienceDirect, SpringerLink, and Ovid databases and references of articles to identify studies reporting data until December 2013. Disease-free survival (DFS) and overall survival (OS) were analyzed by extracting the number of patients with recurrence and survival according to AR expression. RESULTS: There were 16 articles that met the criteria for inclusion in our meta-analysis. DFS and OS were significantly longer in patients with AR expression compared with patients without AR expression (odds ratio [OR], 0.60; 95% confidence interval [CI], 0.40-0.90; OR, 0.53; 95% CI, 0.38-0.73, respectively). In addition, hormone receptor (HR) positive patients had a longer DFS when AR was also expressed (OR, 0.63; 95% CI, 0.41-0.98). For patients with triple negative breast cancer (TNBC), AR expression was also associated with longer DFS and OS (OR, 0.44, 95% CI, 0.26-0.75; OR, 0.26, 95% CI, 0.12-0.55, respectively). Furthermore, AR expression was associated with a longer DFS and OS in women (OR, 0.42, 95% CI, 0.27-0.64; OR, 0.47, 95% CI, 0.38-0.59, respectively). However, in men, AR expression was associated with a worse DFS (OR, 6.00; 95% CI, 1.46-24.73). CONCLUSION: Expression of AR in breast cancer might be associated with better survival outcomes, especially in patients with HR-positive tumors and TNBC, and women. Based on this meta-analysis, we propose that AR expression might be related to prognostic features and contribute to clinical outcomes. Korean Breast Cancer Society 2015-06 2015-06-26 /pmc/articles/PMC4490262/ /pubmed/26155289 http://dx.doi.org/10.4048/jbc.2015.18.2.134 Text en © 2015 Korean Breast Cancer Society. All rights reserved. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Yoonseok
Jae, Eunae
Yoon, Myunghee
Influence of Androgen Receptor Expression on the Survival Outcomes in Breast Cancer: A Meta-Analysis
title Influence of Androgen Receptor Expression on the Survival Outcomes in Breast Cancer: A Meta-Analysis
title_full Influence of Androgen Receptor Expression on the Survival Outcomes in Breast Cancer: A Meta-Analysis
title_fullStr Influence of Androgen Receptor Expression on the Survival Outcomes in Breast Cancer: A Meta-Analysis
title_full_unstemmed Influence of Androgen Receptor Expression on the Survival Outcomes in Breast Cancer: A Meta-Analysis
title_short Influence of Androgen Receptor Expression on the Survival Outcomes in Breast Cancer: A Meta-Analysis
title_sort influence of androgen receptor expression on the survival outcomes in breast cancer: a meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490262/
https://www.ncbi.nlm.nih.gov/pubmed/26155289
http://dx.doi.org/10.4048/jbc.2015.18.2.134
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