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Androgen receptor expression predicts beneficial tamoxifen response in oestrogen receptor-α-negative breast cancer

BACKGROUND: Although the androgen receptor (AR) is frequently expressed in breast cancer, its relevance in the disease is not fully understood. In addition, the relevance of AR in determining tamoxifen treatment efficiency requires evaluation. PURPOSE: To investigate the tamoxifen predictive relevan...

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Autores principales: Hilborn, Erik, Gacic, Jelena, Fornander, Tommy, Nordenskjöld, Bo, Stål, Olle, Jansson, Agneta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742586/
https://www.ncbi.nlm.nih.gov/pubmed/26742006
http://dx.doi.org/10.1038/bjc.2015.464
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author Hilborn, Erik
Gacic, Jelena
Fornander, Tommy
Nordenskjöld, Bo
Stål, Olle
Jansson, Agneta
author_facet Hilborn, Erik
Gacic, Jelena
Fornander, Tommy
Nordenskjöld, Bo
Stål, Olle
Jansson, Agneta
author_sort Hilborn, Erik
collection PubMed
description BACKGROUND: Although the androgen receptor (AR) is frequently expressed in breast cancer, its relevance in the disease is not fully understood. In addition, the relevance of AR in determining tamoxifen treatment efficiency requires evaluation. PURPOSE: To investigate the tamoxifen predictive relevance of the AR protein expression in breast cancer. METHODS: Patients were randomised to tamoxifen 40 mg daily for 2 or 5 years or to no endocrine treatment. Mean follow-up was 15 years. Hazard ratios were calculated with recurrence-free survival as end point. RESULTS: In patients with oestrogen receptor (ER)-negative tumours, expression of AR predicted decreased recurrence rate with tamoxifen (hazard ratio (HR)=0.34; 95% confidence interval (CI)=0.14–0.81; P=0.015), whereas the opposite was seen in the AR− group (HR=2.92; 95% CI=1.16–7.31; P=0.022). Interaction test was significant P<0.001. Patients with triple-negative and AR+ tumours benefitted from tamoxifen treatment (HR=0.12; 95% CI=0.014–0.95 P=0.044), whereas patients with AR− tumours had worse outcome when treated with tamoxifen (HR=3.98; 95% CI=1.32–12.03; P=0.014). Interaction test was significant P=0.003. Patients with ER+ tumours showed benefit from tamoxifen treatment regardless of AR expression. CONCLUSIONS: AR can predict tamoxifen treatment benefit in patients with ER− tumours and triple-negative breast cancer.
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spelling pubmed-47425862017-02-02 Androgen receptor expression predicts beneficial tamoxifen response in oestrogen receptor-α-negative breast cancer Hilborn, Erik Gacic, Jelena Fornander, Tommy Nordenskjöld, Bo Stål, Olle Jansson, Agneta Br J Cancer Clinical Study BACKGROUND: Although the androgen receptor (AR) is frequently expressed in breast cancer, its relevance in the disease is not fully understood. In addition, the relevance of AR in determining tamoxifen treatment efficiency requires evaluation. PURPOSE: To investigate the tamoxifen predictive relevance of the AR protein expression in breast cancer. METHODS: Patients were randomised to tamoxifen 40 mg daily for 2 or 5 years or to no endocrine treatment. Mean follow-up was 15 years. Hazard ratios were calculated with recurrence-free survival as end point. RESULTS: In patients with oestrogen receptor (ER)-negative tumours, expression of AR predicted decreased recurrence rate with tamoxifen (hazard ratio (HR)=0.34; 95% confidence interval (CI)=0.14–0.81; P=0.015), whereas the opposite was seen in the AR− group (HR=2.92; 95% CI=1.16–7.31; P=0.022). Interaction test was significant P<0.001. Patients with triple-negative and AR+ tumours benefitted from tamoxifen treatment (HR=0.12; 95% CI=0.014–0.95 P=0.044), whereas patients with AR− tumours had worse outcome when treated with tamoxifen (HR=3.98; 95% CI=1.32–12.03; P=0.014). Interaction test was significant P=0.003. Patients with ER+ tumours showed benefit from tamoxifen treatment regardless of AR expression. CONCLUSIONS: AR can predict tamoxifen treatment benefit in patients with ER− tumours and triple-negative breast cancer. Nature Publishing Group 2016-02-02 2016-01-07 /pmc/articles/PMC4742586/ /pubmed/26742006 http://dx.doi.org/10.1038/bjc.2015.464 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Clinical Study
Hilborn, Erik
Gacic, Jelena
Fornander, Tommy
Nordenskjöld, Bo
Stål, Olle
Jansson, Agneta
Androgen receptor expression predicts beneficial tamoxifen response in oestrogen receptor-α-negative breast cancer
title Androgen receptor expression predicts beneficial tamoxifen response in oestrogen receptor-α-negative breast cancer
title_full Androgen receptor expression predicts beneficial tamoxifen response in oestrogen receptor-α-negative breast cancer
title_fullStr Androgen receptor expression predicts beneficial tamoxifen response in oestrogen receptor-α-negative breast cancer
title_full_unstemmed Androgen receptor expression predicts beneficial tamoxifen response in oestrogen receptor-α-negative breast cancer
title_short Androgen receptor expression predicts beneficial tamoxifen response in oestrogen receptor-α-negative breast cancer
title_sort androgen receptor expression predicts beneficial tamoxifen response in oestrogen receptor-α-negative breast cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742586/
https://www.ncbi.nlm.nih.gov/pubmed/26742006
http://dx.doi.org/10.1038/bjc.2015.464
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