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Progesterone receptor expression is an independent prognostic variable in early breast cancer: a population-based study

BACKGROUND: Progesterone receptor (PR) expression assessment in early invasive breast cancer remains controversial. This study sought to re-evaluate PR expression as a potential therapeutic guide in early breast cancer; particularly in oestrogen receptor (ER)-positive, lymph node (LN)-negative disea...

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Autores principales: Purdie, C A, Quinlan, P, Jordan, L B, Ashfield, A, Ogston, S, Dewar, J A, Thompson, A M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915123/
https://www.ncbi.nlm.nih.gov/pubmed/24300977
http://dx.doi.org/10.1038/bjc.2013.756
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author Purdie, C A
Quinlan, P
Jordan, L B
Ashfield, A
Ogston, S
Dewar, J A
Thompson, A M
author_facet Purdie, C A
Quinlan, P
Jordan, L B
Ashfield, A
Ogston, S
Dewar, J A
Thompson, A M
author_sort Purdie, C A
collection PubMed
description BACKGROUND: Progesterone receptor (PR) expression assessment in early invasive breast cancer remains controversial. This study sought to re-evaluate PR expression as a potential therapeutic guide in early breast cancer; particularly in oestrogen receptor (ER)-positive, lymph node (LN)-negative disease. METHODS: A population cohort of 1074 patients presenting to a single Cancer Centre over 4 years (2000–2004) underwent surgery for primary invasive breast cancer with curative intent. Prospective data collection included patient demographics, pathology, ER and PR expression, HER2 status, adjuvant chemotherapy and endocrine therapy. Progesterone receptor expression was compared with (all causes) overall survival (OS), breast cancer-specific survival (BCSS) and disease-free survival (DFS). RESULTS: Overall survival was 71.0% and BCSS was 83.0% at median follow-up of 8.34 years. Absent PR expression was significantly associated with poorer prognosis for OS, BCSS and DFS (P<0.0001, log-rank), even within the ER-positive, LN-negative group (hazard ratio for BCSS 3.17, 95% CI 1.43–7.01) and was not influenced by endocrine therapy. Cox's regression analysis demonstrated that PR expression was an independent prognostic variable. CONCLUSION: Absence of PR expression is a powerful, independent prognostic variable in operable, primary breast cancer even in ER-positive, LN-negative patients receiving endocrine therapy. Absence of PR expression should be re-evaluated as a biomarker for poor prognosis in ER-positive breast cancer and such patients considered for additional systemic therapy.
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spelling pubmed-39151232015-02-04 Progesterone receptor expression is an independent prognostic variable in early breast cancer: a population-based study Purdie, C A Quinlan, P Jordan, L B Ashfield, A Ogston, S Dewar, J A Thompson, A M Br J Cancer Clinical Study BACKGROUND: Progesterone receptor (PR) expression assessment in early invasive breast cancer remains controversial. This study sought to re-evaluate PR expression as a potential therapeutic guide in early breast cancer; particularly in oestrogen receptor (ER)-positive, lymph node (LN)-negative disease. METHODS: A population cohort of 1074 patients presenting to a single Cancer Centre over 4 years (2000–2004) underwent surgery for primary invasive breast cancer with curative intent. Prospective data collection included patient demographics, pathology, ER and PR expression, HER2 status, adjuvant chemotherapy and endocrine therapy. Progesterone receptor expression was compared with (all causes) overall survival (OS), breast cancer-specific survival (BCSS) and disease-free survival (DFS). RESULTS: Overall survival was 71.0% and BCSS was 83.0% at median follow-up of 8.34 years. Absent PR expression was significantly associated with poorer prognosis for OS, BCSS and DFS (P<0.0001, log-rank), even within the ER-positive, LN-negative group (hazard ratio for BCSS 3.17, 95% CI 1.43–7.01) and was not influenced by endocrine therapy. Cox's regression analysis demonstrated that PR expression was an independent prognostic variable. CONCLUSION: Absence of PR expression is a powerful, independent prognostic variable in operable, primary breast cancer even in ER-positive, LN-negative patients receiving endocrine therapy. Absence of PR expression should be re-evaluated as a biomarker for poor prognosis in ER-positive breast cancer and such patients considered for additional systemic therapy. Nature Publishing Group 2014-02-04 2013-12-03 /pmc/articles/PMC3915123/ /pubmed/24300977 http://dx.doi.org/10.1038/bjc.2013.756 Text en Copyright © 2014 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Clinical Study
Purdie, C A
Quinlan, P
Jordan, L B
Ashfield, A
Ogston, S
Dewar, J A
Thompson, A M
Progesterone receptor expression is an independent prognostic variable in early breast cancer: a population-based study
title Progesterone receptor expression is an independent prognostic variable in early breast cancer: a population-based study
title_full Progesterone receptor expression is an independent prognostic variable in early breast cancer: a population-based study
title_fullStr Progesterone receptor expression is an independent prognostic variable in early breast cancer: a population-based study
title_full_unstemmed Progesterone receptor expression is an independent prognostic variable in early breast cancer: a population-based study
title_short Progesterone receptor expression is an independent prognostic variable in early breast cancer: a population-based study
title_sort progesterone receptor expression is an independent prognostic variable in early breast cancer: a population-based study
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915123/
https://www.ncbi.nlm.nih.gov/pubmed/24300977
http://dx.doi.org/10.1038/bjc.2013.756
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