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Sex hormone receptor expression and survival in esophageal adenocarcinoma: a prospective cohort study
INTRODUCTION: A striking epidemiological feature of esophageal adenocarcinoma (EAC) is its strong, unexplained male predominance but few studies have evaluated the prevalence of sex hormone receptor expression in EAC. RESULTS: A low proportion of EAC tumors stained positive for ERα (4%) and AR (3%)...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219676/ https://www.ncbi.nlm.nih.gov/pubmed/30450159 http://dx.doi.org/10.18632/oncotarget.26236 |
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author | McMenamin, Úna C. Trainor, James Coleman, Helen G. McManus, Damian T. McQuaid, Stephen Bingham, Victoria James, Jacqueline Salto-Tellez, Manuel Johnston, Brian T. Turkington, Richard C. |
author_facet | McMenamin, Úna C. Trainor, James Coleman, Helen G. McManus, Damian T. McQuaid, Stephen Bingham, Victoria James, Jacqueline Salto-Tellez, Manuel Johnston, Brian T. Turkington, Richard C. |
author_sort | McMenamin, Úna C. |
collection | PubMed |
description | INTRODUCTION: A striking epidemiological feature of esophageal adenocarcinoma (EAC) is its strong, unexplained male predominance but few studies have evaluated the prevalence of sex hormone receptor expression in EAC. RESULTS: A low proportion of EAC tumors stained positive for ERα (4%) and AR (3%) while approximately one third stained positive for ERβ (31%). After a mean follow-up of 3 years (max 9 years), no significant associations were seen for ERα, ERβ or AR expression and EAC recurrence or survival. A non-significant reduction in mortality was observed for positive ERβ tumor expression, when restricting to patients with gastro-esophageal junctional (GEJ) cancer (HR 0.58, 95% CI 0.33, 1.03, p = 0.06). MATERIALS AND METHODS: We identified all EAC patients who underwent neo-adjuvant chemotherapy prior to surgical resection between 2004–2012 in the Northern Ireland Cancer Centre. Immunohistochemical expression of ERα, ERβ and AR was scored on triplicate cores to generate H-scores. Cox proportional hazards regression was used to evaluate the association between sex hormone receptor expression and overall, cancer-specific and recurrence-free survival. CONCLUSION: We found little evidence of ERα or AR expression in EAC. A moderate proportion expressed ERβ and there was suggestive evidence that its expression was associated with improved survival in GEJ cancer patients. |
format | Online Article Text |
id | pubmed-6219676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-62196762018-11-16 Sex hormone receptor expression and survival in esophageal adenocarcinoma: a prospective cohort study McMenamin, Úna C. Trainor, James Coleman, Helen G. McManus, Damian T. McQuaid, Stephen Bingham, Victoria James, Jacqueline Salto-Tellez, Manuel Johnston, Brian T. Turkington, Richard C. Oncotarget Research Paper INTRODUCTION: A striking epidemiological feature of esophageal adenocarcinoma (EAC) is its strong, unexplained male predominance but few studies have evaluated the prevalence of sex hormone receptor expression in EAC. RESULTS: A low proportion of EAC tumors stained positive for ERα (4%) and AR (3%) while approximately one third stained positive for ERβ (31%). After a mean follow-up of 3 years (max 9 years), no significant associations were seen for ERα, ERβ or AR expression and EAC recurrence or survival. A non-significant reduction in mortality was observed for positive ERβ tumor expression, when restricting to patients with gastro-esophageal junctional (GEJ) cancer (HR 0.58, 95% CI 0.33, 1.03, p = 0.06). MATERIALS AND METHODS: We identified all EAC patients who underwent neo-adjuvant chemotherapy prior to surgical resection between 2004–2012 in the Northern Ireland Cancer Centre. Immunohistochemical expression of ERα, ERβ and AR was scored on triplicate cores to generate H-scores. Cox proportional hazards regression was used to evaluate the association between sex hormone receptor expression and overall, cancer-specific and recurrence-free survival. CONCLUSION: We found little evidence of ERα or AR expression in EAC. A moderate proportion expressed ERβ and there was suggestive evidence that its expression was associated with improved survival in GEJ cancer patients. Impact Journals LLC 2018-10-19 /pmc/articles/PMC6219676/ /pubmed/30450159 http://dx.doi.org/10.18632/oncotarget.26236 Text en Copyright: © 2018 McMenamin et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper McMenamin, Úna C. Trainor, James Coleman, Helen G. McManus, Damian T. McQuaid, Stephen Bingham, Victoria James, Jacqueline Salto-Tellez, Manuel Johnston, Brian T. Turkington, Richard C. Sex hormone receptor expression and survival in esophageal adenocarcinoma: a prospective cohort study |
title | Sex hormone receptor expression and survival in esophageal adenocarcinoma: a prospective cohort study |
title_full | Sex hormone receptor expression and survival in esophageal adenocarcinoma: a prospective cohort study |
title_fullStr | Sex hormone receptor expression and survival in esophageal adenocarcinoma: a prospective cohort study |
title_full_unstemmed | Sex hormone receptor expression and survival in esophageal adenocarcinoma: a prospective cohort study |
title_short | Sex hormone receptor expression and survival in esophageal adenocarcinoma: a prospective cohort study |
title_sort | sex hormone receptor expression and survival in esophageal adenocarcinoma: a prospective cohort study |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219676/ https://www.ncbi.nlm.nih.gov/pubmed/30450159 http://dx.doi.org/10.18632/oncotarget.26236 |
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