Abstract

IntroductionBreast cancers are traditionally divided into hormone-receptor positive and negative cases. This classification helps to guide patient management. However, a subgroup of hormone-receptor positive patients relapse irrespective of hormonal therapy. Gene expression profiling has classified breast tumours into five major subtypes with significant different outcome. The two luminal subtypes, A and B, show high expression of ESR1, GATA3 and FOXA1 genes. Prognostic biomarkers for oestrogen receptor (ER)-positive cases include progesterone receptor (PR) and androgen receptor (AR), and proteins related to proliferation or apoptotic resistance. The aim of this study was to identify the best predictors of success of hormonal therapy.MethodsBy immunohistochemistry we studied 10 markers in a consecutive series of 832 cases of breast carcinoma treated at the Paoli-Calmettes Institute from 1990 to 2002 and deposited onto tissue microarrays (TMA). These markers were luminal-related markers ER, PR, AR, FOXA1 and GATA3 transcription factors, proliferation-related Ki67 and CCND1, ERBB2, anti-apoptotic BCL2 and P53. We also measured vascular peritumoural invasion (VPI), size, grade and lymph node involvement. For 143 cases, gene expression profiles were available. Adjuvant chemotherapy and hormonal therapy were given to high- and low-risk patients, respectively. The 162 events observed and taken into account were metastases.ResultsMolecular expression of the 10 parameters and subtype with ER status were strongly correlated. Of the 67 luminal A cases of this series, 63 were ER-positive. Multivariate analyses showed the highly significant prognostic value of VPI (hazard ratio (HR) = 2.47), Ki67 (HR = 2.9), P53 (HR = 2.9) and GATA3 (HR = 0.5) for the 240 patients who received hormonal therapy.ConclusionsA panel of three antibodies (Ki67, P53 and GATA3) associated with VPI can significantly improve the traditional prognosticators in predicting outcome for ER-positive breast cancer patients receiving hormonal therapy.

Highlights

  • Breast cancers are traditionally divided into hormone-receptor positive and negative cases

  • By immunohistochemistry we studied 10 markers in a consecutive series of 832 cases of breast carcinoma treated at the Paoli-Calmettes Institute from 1990 to 2002 and deposited onto tissue microarrays (TMA)

  • A panel of three antibodies (Ki67, P53 and GATA3) associated with vascular peritumoural invasion (VPI) can significantly improve the traditional prognosticators in predicting outcome for ER-positive breast cancer patients receiving hormonal therapy

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Summary

Introduction

Breast cancers are traditionally divided into hormone-receptor positive and negative cases. This classification helps to guide patient management. A subgroup of hormone-receptor positive patients relapse irrespective of hormonal therapy. Gene expression profiling has classified breast tumours into five major subtypes with significant different outcome. The two luminal subtypes, A and B, show high expression of ESR1, GATA3 and FOXA1 genes. The traditional division of breast cancers into hormone receptor positive and negative cases helps to guide patient management. A subgroup of hormone receptor-positive patients relapse irrespective of standard hormonal therapy. Gene expression profiling has classified breast tumours into five major molecular subtypes with different outcomes. The two luminal subtypes, A and B, express the ESR1, GATA3 and FOXA1 genes [1]. There are few indicators to determine if AR: androgen receptor; CI: confidence interval; ER: oestrogen receptor; H&E: haematoxylin and eosin; HR: hazard ratio; MFS: metastasis-free survival; NSABP: National Surgical Adjuvant Breast and Bowel Project; PCR: polymerase chain reaction; PR: progesterone receptor; QS: quick score; RS: recurrence score; TMA: tissue microarrays; TNM: tumour node metastasis; VPI: vascular peritumoural invasion

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