Triple-negative breast cancer with brain metastases: a comparison between basal-like and non-basal-like biological subtypes

The aim of this study was to divide the group of triple-negative breast cancer patients with brain metastases into basal-like and non-basal-like biological subtypes in order to compare clinical features and survival rates in those two groups. A comprehensive analysis of 111 consecutive triple-negati...

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Main Authors: Niwińska, Anna, Olszewski, Wojciech, Murawska, Magdalena, Pogoda, Katarzyna
Format: Online
Language:English
Published: Springer US 2011
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215879/
id pubmed-3215879
recordtype oai_dc
spelling pubmed-32158792011-12-09 Triple-negative breast cancer with brain metastases: a comparison between basal-like and non-basal-like biological subtypes Niwińska, Anna Olszewski, Wojciech Murawska, Magdalena Pogoda, Katarzyna Clinical Study – Patient Study The aim of this study was to divide the group of triple-negative breast cancer patients with brain metastases into basal-like and non-basal-like biological subtypes in order to compare clinical features and survival rates in those two groups. A comprehensive analysis of 111 consecutive triple-negative breast cancer patients with brain metastases treated in the years 2003–2009 was performed. In 75 patients, immunohistochemistry was used as a surrogate of microarray in order to evaluate the expression of three basal markers: cytokeratin 5/6 (CK 5/6), EGFR/HER1 and c-KIT. The basal-like (ER/PgR/HER2-negative, CK5/6positive and/or HER1-positive) and non-basal-like (ER/PgR/HER2-negative, CK5/6-negative, HER1-negative) subsets were selected. Clinical features and survivals were compared in both groups. In the group of 111 triple-negative breast cancer patients, median DFS, OS and survival from brain metastases were 20, 29 and 4 months, respectively. In 75 patients who were evaluable for basal markers, median DFS, OS and survival from brain metastases were 18, 26 and 3.2 months, respectively. In the basal-like subtype, the survival rates were 15, 26 and 3 months, respectively, and in the non-basal-like subtypes, they were 20, 30 and 2.8 months, respectively. No statistically significant differences in survivals were detected between the basal-like and non-basal-like biological subtypes. Factors influencing survival from brain metastases were: Karnofsky performance status (KPS), the status of extracranial disease and age. Biological markers differentiating triple-negative group into basal-like and non-basal-like subtype (CK 5/6, HER1, c-KIT) had no influence on survival. In patients with triple-negative breast cancer and brain metastases, well-known clinical, but not molecular, features correlated with survival. Springer US 2011-06-09 2011-12 /pmc/articles/PMC3215879/ /pubmed/21656328 http://dx.doi.org/10.1007/s11060-011-0616-3 Text en © The Author(s) 2011
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Niwińska, Anna
Olszewski, Wojciech
Murawska, Magdalena
Pogoda, Katarzyna
spellingShingle Niwińska, Anna
Olszewski, Wojciech
Murawska, Magdalena
Pogoda, Katarzyna
Triple-negative breast cancer with brain metastases: a comparison between basal-like and non-basal-like biological subtypes
author_facet Niwińska, Anna
Olszewski, Wojciech
Murawska, Magdalena
Pogoda, Katarzyna
author_sort Niwińska, Anna
title Triple-negative breast cancer with brain metastases: a comparison between basal-like and non-basal-like biological subtypes
title_short Triple-negative breast cancer with brain metastases: a comparison between basal-like and non-basal-like biological subtypes
title_full Triple-negative breast cancer with brain metastases: a comparison between basal-like and non-basal-like biological subtypes
title_fullStr Triple-negative breast cancer with brain metastases: a comparison between basal-like and non-basal-like biological subtypes
title_full_unstemmed Triple-negative breast cancer with brain metastases: a comparison between basal-like and non-basal-like biological subtypes
title_sort triple-negative breast cancer with brain metastases: a comparison between basal-like and non-basal-like biological subtypes
description The aim of this study was to divide the group of triple-negative breast cancer patients with brain metastases into basal-like and non-basal-like biological subtypes in order to compare clinical features and survival rates in those two groups. A comprehensive analysis of 111 consecutive triple-negative breast cancer patients with brain metastases treated in the years 2003–2009 was performed. In 75 patients, immunohistochemistry was used as a surrogate of microarray in order to evaluate the expression of three basal markers: cytokeratin 5/6 (CK 5/6), EGFR/HER1 and c-KIT. The basal-like (ER/PgR/HER2-negative, CK5/6positive and/or HER1-positive) and non-basal-like (ER/PgR/HER2-negative, CK5/6-negative, HER1-negative) subsets were selected. Clinical features and survivals were compared in both groups. In the group of 111 triple-negative breast cancer patients, median DFS, OS and survival from brain metastases were 20, 29 and 4 months, respectively. In 75 patients who were evaluable for basal markers, median DFS, OS and survival from brain metastases were 18, 26 and 3.2 months, respectively. In the basal-like subtype, the survival rates were 15, 26 and 3 months, respectively, and in the non-basal-like subtypes, they were 20, 30 and 2.8 months, respectively. No statistically significant differences in survivals were detected between the basal-like and non-basal-like biological subtypes. Factors influencing survival from brain metastases were: Karnofsky performance status (KPS), the status of extracranial disease and age. Biological markers differentiating triple-negative group into basal-like and non-basal-like subtype (CK 5/6, HER1, c-KIT) had no influence on survival. In patients with triple-negative breast cancer and brain metastases, well-known clinical, but not molecular, features correlated with survival.
publisher Springer US
publishDate 2011
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215879/
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