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Prognostic value of androgen receptor and FOXA1 co-expression in non-metastatic triple negative breast cancer and correlation with other biomarkers

Authors :
Céline Charon-Barra
William Jacot
Marian Gutowski
Florence Boissière
Caroline Mollevi
Céline Bourgier
Gilles Romieu
Pierre-Jean Lamy
Evelyne Crapez
Elodie Chartron
Séverine Guiu
Joelle Simony-Lafontaine
Département d'oncologie Médicale
CRLCC Val d'Aurelle - Paul Lamarque
Institut de Recherche en Cancérologie de Montpellier (IRCM - U1194 Inserm - UM)
CRLCC Val d'Aurelle - Paul Lamarque-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)
CRLC Val d'Aurelle-Paul Lamarque
Centre Régional de Lutte contre le cancer Georges-François Leclerc [Dijon] (UNICANCER/CRLCC-CGFL)
UNICANCER
Département de chirurgie
Herrada, Anthony
Source :
British Journal of Cancer, British Journal of Cancer, Cancer Research UK, 2018, 119 (1), pp.76-79. ⟨10.1038/s41416-018-0142-6⟩
Publication Year :
2018
Publisher :
HAL CCSD, 2018.

Abstract

International audience; BACKGROUND: In luminal androgen receptor (AR) tumours, FOXA1 may direct AR to sites occupied by ER in luminal tumours, thus stimulating proliferation.METHODS: AR and FOXA1 expression were evaluated by immunohistochemistry in 333 non-metastatic triple-negative breast cancers (TNBC). Positivity threshold was set at ≥ 1% staining. Lymphocytic infiltration, PD-L1expression, PIK3CA mutations, PTEN defects and BRCA1 promoter methylation were assessed.RESULTS: AR + /FOXA1 + tumours (42.4%) were more frequently: found in older patients, lobular, of lower nuclear grade, with more frequently PIK3CA mutations; exhibited less frequently BRCA1 promoter methylation, defects of PTEN and PD-L1 expression than others. Recurrence-free and overall survivals were significantly lower for AR + /FOXA1 + TNBC (median follow-up: 7.8 years).CONCLUSIONS: AR + /FOXA1 + expression defines a luminal-like TNBC subgroup affected with a worse outcome compared to other TNBC and a higher risk of late recurrences. This subgroup appears enriched in PIK3CA mutations, suggesting a role for PI3K inhibitors in this subgroup.

Details

Language :
English
ISSN :
00070920 and 15321827
Database :
OpenAIRE
Journal :
British Journal of Cancer, British Journal of Cancer, Cancer Research UK, 2018, 119 (1), pp.76-79. ⟨10.1038/s41416-018-0142-6⟩
Accession number :
edsair.doi.dedup.....6a5aac4e411ed03049e7f19574cf27a5