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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3496146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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