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PIK3CA mutation impact on survival in breast cancer patients and in ERα, PR and ERBB2-based subgroups

INTRODUCTION: PIK3CA is the oncogene showing the highest frequency of gain-of-function mutations in breast cancer, but the prognostic value of PIK3CA mutation status is controversial. METHODS: We investigated the prognostic significance of PIK3CA mutation status in a series of 452 patients with unil...

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Autores principales: Cizkova, Magdalena, Susini, Aurélie, Vacher, Sophie, Cizeron-Clairac, Géraldine, Andrieu, Catherine, Driouch, Keltouma, Fourme, Emmanuelle, Lidereau, Rosette, Bièche, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496146/
https://www.ncbi.nlm.nih.gov/pubmed/22330809
http://dx.doi.org/10.1186/bcr3113
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author Cizkova, Magdalena
Susini, Aurélie
Vacher, Sophie
Cizeron-Clairac, Géraldine
Andrieu, Catherine
Driouch, Keltouma
Fourme, Emmanuelle
Lidereau, Rosette
Bièche, Ivan
author_facet Cizkova, Magdalena
Susini, Aurélie
Vacher, Sophie
Cizeron-Clairac, Géraldine
Andrieu, Catherine
Driouch, Keltouma
Fourme, Emmanuelle
Lidereau, Rosette
Bièche, Ivan
author_sort Cizkova, Magdalena
collection PubMed
description INTRODUCTION: PIK3CA is the oncogene showing the highest frequency of gain-of-function mutations in breast cancer, but the prognostic value of PIK3CA mutation status is controversial. METHODS: We investigated the prognostic significance of PIK3CA mutation status in a series of 452 patients with unilateral invasive primary breast cancer and known long-term outcome (median follow-up 10 years). RESULTS: PIK3CA mutations were identified in 151 tumors (33.4%). The frequency of PIK3CA mutations differed markedly according to hormone receptor (estrogen receptor alpha [ERα] and progesterone receptor [PR]) and ERBB2 status, ranging from 12.5% in the triple-negative subgroup (ER-/PR-/ERBB2-) to 41.1% in the HR+/ERBB2- subgroup. PIK3CA mutation was associated with significantly longer metastasis-free survival in the overall population (P = 0.0056), and especially in the PR-positive and ERBB2-positive subgroups. In Cox multivariate regression analysis, the prognostic significance of PIK3CA mutation status persisted only in the ERBB2-positive subgroup. CONCLUSIONS: This study confirms the high prevalence of PIK3CA mutations in breast cancer. PIK3CA mutation is an emerging tumor marker which might become used in treatment-choosing process. The independent prognostic value of PIK3CA mutation status in ERBB2-positive breast cancer patients should be now confirmed in larger series of patients included in randomized prospective ERBB2-based clinical trials.
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spelling pubmed-34961462012-11-14 PIK3CA mutation impact on survival in breast cancer patients and in ERα, PR and ERBB2-based subgroups Cizkova, Magdalena Susini, Aurélie Vacher, Sophie Cizeron-Clairac, Géraldine Andrieu, Catherine Driouch, Keltouma Fourme, Emmanuelle Lidereau, Rosette Bièche, Ivan Breast Cancer Res Research Article INTRODUCTION: PIK3CA is the oncogene showing the highest frequency of gain-of-function mutations in breast cancer, but the prognostic value of PIK3CA mutation status is controversial. METHODS: We investigated the prognostic significance of PIK3CA mutation status in a series of 452 patients with unilateral invasive primary breast cancer and known long-term outcome (median follow-up 10 years). RESULTS: PIK3CA mutations were identified in 151 tumors (33.4%). The frequency of PIK3CA mutations differed markedly according to hormone receptor (estrogen receptor alpha [ERα] and progesterone receptor [PR]) and ERBB2 status, ranging from 12.5% in the triple-negative subgroup (ER-/PR-/ERBB2-) to 41.1% in the HR+/ERBB2- subgroup. PIK3CA mutation was associated with significantly longer metastasis-free survival in the overall population (P = 0.0056), and especially in the PR-positive and ERBB2-positive subgroups. In Cox multivariate regression analysis, the prognostic significance of PIK3CA mutation status persisted only in the ERBB2-positive subgroup. CONCLUSIONS: This study confirms the high prevalence of PIK3CA mutations in breast cancer. PIK3CA mutation is an emerging tumor marker which might become used in treatment-choosing process. The independent prognostic value of PIK3CA mutation status in ERBB2-positive breast cancer patients should be now confirmed in larger series of patients included in randomized prospective ERBB2-based clinical trials. BioMed Central 2012 2012-02-13 /pmc/articles/PMC3496146/ /pubmed/22330809 http://dx.doi.org/10.1186/bcr3113 Text en Copyright ©2012 Cizkova et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Cizkova, Magdalena
Susini, Aurélie
Vacher, Sophie
Cizeron-Clairac, Géraldine
Andrieu, Catherine
Driouch, Keltouma
Fourme, Emmanuelle
Lidereau, Rosette
Bièche, Ivan
PIK3CA mutation impact on survival in breast cancer patients and in ERα, PR and ERBB2-based subgroups
title PIK3CA mutation impact on survival in breast cancer patients and in ERα, PR and ERBB2-based subgroups
title_full PIK3CA mutation impact on survival in breast cancer patients and in ERα, PR and ERBB2-based subgroups
title_fullStr PIK3CA mutation impact on survival in breast cancer patients and in ERα, PR and ERBB2-based subgroups
title_full_unstemmed PIK3CA mutation impact on survival in breast cancer patients and in ERα, PR and ERBB2-based subgroups
title_short PIK3CA mutation impact on survival in breast cancer patients and in ERα, PR and ERBB2-based subgroups
title_sort pik3ca mutation impact on survival in breast cancer patients and in erα, pr and erbb2-based subgroups
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496146/
https://www.ncbi.nlm.nih.gov/pubmed/22330809
http://dx.doi.org/10.1186/bcr3113
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