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A clinically applicable molecular classification for high-grade serous ovarian cancer based on hormone receptor expression

To establish an effective hormone receptor-based molecular classification of high-grade serous ovarian cancer (HGSC), we retrospectively examined 875 consecutive HGSC patients who underwent primary surgery at our hospital and constructed tissue microarrays from these specimens. The expression levels...

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Autores principales: Feng, Zheng, Wen, Hao, Bi, Rui, Ju, Xingzhu, Chen, Xiaojun, Yang, Wentao, Wu, Xiaohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853732/
https://www.ncbi.nlm.nih.gov/pubmed/27139372
http://dx.doi.org/10.1038/srep25408
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author Feng, Zheng
Wen, Hao
Bi, Rui
Ju, Xingzhu
Chen, Xiaojun
Yang, Wentao
Wu, Xiaohua
author_facet Feng, Zheng
Wen, Hao
Bi, Rui
Ju, Xingzhu
Chen, Xiaojun
Yang, Wentao
Wu, Xiaohua
author_sort Feng, Zheng
collection PubMed
description To establish an effective hormone receptor-based molecular classification of high-grade serous ovarian cancer (HGSC), we retrospectively examined 875 consecutive HGSC patients who underwent primary surgery at our hospital and constructed tissue microarrays from these specimens. The expression levels of the hormone receptors were as follows: ER 64.4%, PR 12.6%, AR 35.6%, FSHR 54.5%, LHR 34.8%, and GnRHR 88.3%. Based on clustering of their expression patterns, we classified patients into five subgroups with distinctive clinical features (PR+, PR − ER + AR+, PR − ER + AR−, PR − ER − AR+, and PR − ER − AR−). Patients in the PR + group were younger compared to those in the other groups (p < 0.001). More patients were of advanced stage in the PR − ER + AR− group than the other groups (p = 0.020). A greater proportion of patients were sensitive to platinum-based chemotherapy in the PR − ER − AR + group compared with the other groups (p = 0.034). A trend of increasing risk of death was observed among these subgroups (p < 0.001). In the multivariate analysis, patients also had orderly increased hazard ratios for death in the PR + (HR = 2.256, 95% CI, 0.983–5.175), PR − ER + AR + (HR = 2.188, 95% CI, 1.004–4.796), PR − ER − AR− (HR = 2.316, 95% CI, 1.097–5.082) and PR − ER + AR− (HR = 2.928, 95% CI, 1.366–6.276) subgroups compared to the PR − ER − AR+ subgroup. Our classification could help predict patient clinical outcomes, guide individual treatments and stratify patients in future clinical trials.
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spelling pubmed-48537322016-05-16 A clinically applicable molecular classification for high-grade serous ovarian cancer based on hormone receptor expression Feng, Zheng Wen, Hao Bi, Rui Ju, Xingzhu Chen, Xiaojun Yang, Wentao Wu, Xiaohua Sci Rep Article To establish an effective hormone receptor-based molecular classification of high-grade serous ovarian cancer (HGSC), we retrospectively examined 875 consecutive HGSC patients who underwent primary surgery at our hospital and constructed tissue microarrays from these specimens. The expression levels of the hormone receptors were as follows: ER 64.4%, PR 12.6%, AR 35.6%, FSHR 54.5%, LHR 34.8%, and GnRHR 88.3%. Based on clustering of their expression patterns, we classified patients into five subgroups with distinctive clinical features (PR+, PR − ER + AR+, PR − ER + AR−, PR − ER − AR+, and PR − ER − AR−). Patients in the PR + group were younger compared to those in the other groups (p < 0.001). More patients were of advanced stage in the PR − ER + AR− group than the other groups (p = 0.020). A greater proportion of patients were sensitive to platinum-based chemotherapy in the PR − ER − AR + group compared with the other groups (p = 0.034). A trend of increasing risk of death was observed among these subgroups (p < 0.001). In the multivariate analysis, patients also had orderly increased hazard ratios for death in the PR + (HR = 2.256, 95% CI, 0.983–5.175), PR − ER + AR + (HR = 2.188, 95% CI, 1.004–4.796), PR − ER − AR− (HR = 2.316, 95% CI, 1.097–5.082) and PR − ER + AR− (HR = 2.928, 95% CI, 1.366–6.276) subgroups compared to the PR − ER − AR+ subgroup. Our classification could help predict patient clinical outcomes, guide individual treatments and stratify patients in future clinical trials. Nature Publishing Group 2016-05-03 /pmc/articles/PMC4853732/ /pubmed/27139372 http://dx.doi.org/10.1038/srep25408 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Feng, Zheng
Wen, Hao
Bi, Rui
Ju, Xingzhu
Chen, Xiaojun
Yang, Wentao
Wu, Xiaohua
A clinically applicable molecular classification for high-grade serous ovarian cancer based on hormone receptor expression
title A clinically applicable molecular classification for high-grade serous ovarian cancer based on hormone receptor expression
title_full A clinically applicable molecular classification for high-grade serous ovarian cancer based on hormone receptor expression
title_fullStr A clinically applicable molecular classification for high-grade serous ovarian cancer based on hormone receptor expression
title_full_unstemmed A clinically applicable molecular classification for high-grade serous ovarian cancer based on hormone receptor expression
title_short A clinically applicable molecular classification for high-grade serous ovarian cancer based on hormone receptor expression
title_sort clinically applicable molecular classification for high-grade serous ovarian cancer based on hormone receptor expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853732/
https://www.ncbi.nlm.nih.gov/pubmed/27139372
http://dx.doi.org/10.1038/srep25408
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