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Correlation between estrogen receptor expression and prognosis in epithelial ovarian cancer: a meta-analysis

OBJECTIVE: Accumulated studies have investigated the prognostic significance of estrogen receptor expression in epithelial ovarian cancer, but results remain controversial. The aim of this study was to perform a meta-analysis to clarify the prognostic value of estrogen receptor expression in epithel...

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Autores principales: Shen, Zhaojun, Luo, Hui, Li, Saisai, Sheng, Bo, Zhao, Menghuang, Zhu, Haiyan, Zhu, Xueqiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617514/
https://www.ncbi.nlm.nih.gov/pubmed/28977954
http://dx.doi.org/10.18632/oncotarget.18253
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author Shen, Zhaojun
Luo, Hui
Li, Saisai
Sheng, Bo
Zhao, Menghuang
Zhu, Haiyan
Zhu, Xueqiong
author_facet Shen, Zhaojun
Luo, Hui
Li, Saisai
Sheng, Bo
Zhao, Menghuang
Zhu, Haiyan
Zhu, Xueqiong
author_sort Shen, Zhaojun
collection PubMed
description OBJECTIVE: Accumulated studies have investigated the prognostic significance of estrogen receptor expression in epithelial ovarian cancer, but results remain controversial. The aim of this study was to perform a meta-analysis to clarify the prognostic value of estrogen receptor expression in epithelial ovarian cancer. METHODS: A systematic search was performed in PUBMED, EMBASE, and COCHRANE databases to identify relevant studies up to December 2016. The pooled hazard rates (HR) with 95% confidence intervals (CIs) for overall survival and time to tumor progression were calculated and then weighted and pooled in this meta-analysis with a random-effect model. RESULTS: Thirty-five studies with a total of 5824 patients were included. In brief, the expression of estrogen receptor was associated with an improved overall survival (HR = 0.86, 95% CI = 0.76-0.97), whereas there was no significant difference between estrogen receptor and time to tumor progression among epithelial ovarian cancer patients. Subgroup analysis revealed that estrogen receptor expression was significantly correlated with overall survival in different subgroups, such as in unclassified epithelial ovarian cancer (HR= 0.80, 95% CI = 0.66-0.95), studies using immunohistochemistry detection method (HR= 0.85, 95% CI = 0.73-1.00), European population (HR= 0.75, 95% CI = 0.60-0.94) and estrogen receptor α subtype (HR= 0.78, 95% CI = 0.62-0.98). CONCLUSIONS: Estrogen receptor, especially estrogen receptor α, was associated with an improved overall survival in epithelial ovarian cancer. Estrogen receptor expression may be a promising prognostic factor in epithelial ovarian cancer patients.
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spelling pubmed-56175142017-10-03 Correlation between estrogen receptor expression and prognosis in epithelial ovarian cancer: a meta-analysis Shen, Zhaojun Luo, Hui Li, Saisai Sheng, Bo Zhao, Menghuang Zhu, Haiyan Zhu, Xueqiong Oncotarget Meta-Analysis OBJECTIVE: Accumulated studies have investigated the prognostic significance of estrogen receptor expression in epithelial ovarian cancer, but results remain controversial. The aim of this study was to perform a meta-analysis to clarify the prognostic value of estrogen receptor expression in epithelial ovarian cancer. METHODS: A systematic search was performed in PUBMED, EMBASE, and COCHRANE databases to identify relevant studies up to December 2016. The pooled hazard rates (HR) with 95% confidence intervals (CIs) for overall survival and time to tumor progression were calculated and then weighted and pooled in this meta-analysis with a random-effect model. RESULTS: Thirty-five studies with a total of 5824 patients were included. In brief, the expression of estrogen receptor was associated with an improved overall survival (HR = 0.86, 95% CI = 0.76-0.97), whereas there was no significant difference between estrogen receptor and time to tumor progression among epithelial ovarian cancer patients. Subgroup analysis revealed that estrogen receptor expression was significantly correlated with overall survival in different subgroups, such as in unclassified epithelial ovarian cancer (HR= 0.80, 95% CI = 0.66-0.95), studies using immunohistochemistry detection method (HR= 0.85, 95% CI = 0.73-1.00), European population (HR= 0.75, 95% CI = 0.60-0.94) and estrogen receptor α subtype (HR= 0.78, 95% CI = 0.62-0.98). CONCLUSIONS: Estrogen receptor, especially estrogen receptor α, was associated with an improved overall survival in epithelial ovarian cancer. Estrogen receptor expression may be a promising prognostic factor in epithelial ovarian cancer patients. Impact Journals LLC 2017-05-29 /pmc/articles/PMC5617514/ /pubmed/28977954 http://dx.doi.org/10.18632/oncotarget.18253 Text en Copyright: © 2017 Shen et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Meta-Analysis
Shen, Zhaojun
Luo, Hui
Li, Saisai
Sheng, Bo
Zhao, Menghuang
Zhu, Haiyan
Zhu, Xueqiong
Correlation between estrogen receptor expression and prognosis in epithelial ovarian cancer: a meta-analysis
title Correlation between estrogen receptor expression and prognosis in epithelial ovarian cancer: a meta-analysis
title_full Correlation between estrogen receptor expression and prognosis in epithelial ovarian cancer: a meta-analysis
title_fullStr Correlation between estrogen receptor expression and prognosis in epithelial ovarian cancer: a meta-analysis
title_full_unstemmed Correlation between estrogen receptor expression and prognosis in epithelial ovarian cancer: a meta-analysis
title_short Correlation between estrogen receptor expression and prognosis in epithelial ovarian cancer: a meta-analysis
title_sort correlation between estrogen receptor expression and prognosis in epithelial ovarian cancer: a meta-analysis
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617514/
https://www.ncbi.nlm.nih.gov/pubmed/28977954
http://dx.doi.org/10.18632/oncotarget.18253
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