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Clinical outcome of brain metastases differs significantly among breast cancer subtypes

Brain metastases in patients with breast cancer are associated with a poor survival rate. A small number of studies have challenged this premise, suggesting that survival times following brain metastasis differ significantly between breast cancer subtypes. In the current study, overall survival (OS)...

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Autores principales: Oehrlich, Nadja E., Spineli, Loukia M., Papendorf, Frank, Park-Simon, Tjoung-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494902/
https://www.ncbi.nlm.nih.gov/pubmed/28693153
http://dx.doi.org/10.3892/ol.2017.6166
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author Oehrlich, Nadja E.
Spineli, Loukia M.
Papendorf, Frank
Park-Simon, Tjoung-Won
author_facet Oehrlich, Nadja E.
Spineli, Loukia M.
Papendorf, Frank
Park-Simon, Tjoung-Won
author_sort Oehrlich, Nadja E.
collection PubMed
description Brain metastases in patients with breast cancer are associated with a poor survival rate. A small number of studies have challenged this premise, suggesting that survival times following brain metastasis differ significantly between breast cancer subtypes. In the current study, overall survival (OS), brain metastases-free survival (BMFS) and survival following brain metastases (SFBM) were found to be associated with the intrinsic breast cancer subtype. A total of 1,147 patients with invasive breast cancer who were treated at the Hannover Medical School between January 2004 and December 2010 were included, from which 54 patients with brain metastases were identified. The Kaplan-Meier method or Cox regression analyses were performed for analysis of survival. OS was found to differ significantly between breast cancer subtypes: OS was significantly shorter in patients with triple-negative (TN) cancer compared with patients with human epidermal growth factor receptor (HER2)-enriched tumors (P<0.001). In addition, median BMFS times differed significantly between luminal (1,003 days), HER2-enriched (514 days) and TN breast cancer patients (460 days) (P=0.045). The median durations of SFBM were 386 days in luminal, 310 days in HER2-enriched and 147 days in TN breast cancer patients (P=0.029). The results suggested that patients with luminal breast cancer have a lower risk of brain metastases and the most favorable outcome with regard to BMFS, whereas patients with HER2-positive or TN breast cancer have a significantly higher risk of developing brain metastases. Compared with TN breast cancer, the duration of SFBM was doubled in HER2-enriched cancers. These findings may have important implications for treatment and follow-up strategies in patients with breast cancer.
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spelling pubmed-54949022017-07-07 Clinical outcome of brain metastases differs significantly among breast cancer subtypes Oehrlich, Nadja E. Spineli, Loukia M. Papendorf, Frank Park-Simon, Tjoung-Won Oncol Lett Articles Brain metastases in patients with breast cancer are associated with a poor survival rate. A small number of studies have challenged this premise, suggesting that survival times following brain metastasis differ significantly between breast cancer subtypes. In the current study, overall survival (OS), brain metastases-free survival (BMFS) and survival following brain metastases (SFBM) were found to be associated with the intrinsic breast cancer subtype. A total of 1,147 patients with invasive breast cancer who were treated at the Hannover Medical School between January 2004 and December 2010 were included, from which 54 patients with brain metastases were identified. The Kaplan-Meier method or Cox regression analyses were performed for analysis of survival. OS was found to differ significantly between breast cancer subtypes: OS was significantly shorter in patients with triple-negative (TN) cancer compared with patients with human epidermal growth factor receptor (HER2)-enriched tumors (P<0.001). In addition, median BMFS times differed significantly between luminal (1,003 days), HER2-enriched (514 days) and TN breast cancer patients (460 days) (P=0.045). The median durations of SFBM were 386 days in luminal, 310 days in HER2-enriched and 147 days in TN breast cancer patients (P=0.029). The results suggested that patients with luminal breast cancer have a lower risk of brain metastases and the most favorable outcome with regard to BMFS, whereas patients with HER2-positive or TN breast cancer have a significantly higher risk of developing brain metastases. Compared with TN breast cancer, the duration of SFBM was doubled in HER2-enriched cancers. These findings may have important implications for treatment and follow-up strategies in patients with breast cancer. D.A. Spandidos 2017-07 2017-05-12 /pmc/articles/PMC5494902/ /pubmed/28693153 http://dx.doi.org/10.3892/ol.2017.6166 Text en Copyright: © Oehrlich et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Oehrlich, Nadja E.
Spineli, Loukia M.
Papendorf, Frank
Park-Simon, Tjoung-Won
Clinical outcome of brain metastases differs significantly among breast cancer subtypes
title Clinical outcome of brain metastases differs significantly among breast cancer subtypes
title_full Clinical outcome of brain metastases differs significantly among breast cancer subtypes
title_fullStr Clinical outcome of brain metastases differs significantly among breast cancer subtypes
title_full_unstemmed Clinical outcome of brain metastases differs significantly among breast cancer subtypes
title_short Clinical outcome of brain metastases differs significantly among breast cancer subtypes
title_sort clinical outcome of brain metastases differs significantly among breast cancer subtypes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494902/
https://www.ncbi.nlm.nih.gov/pubmed/28693153
http://dx.doi.org/10.3892/ol.2017.6166
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