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Clinical significance of morphologic characteristics in triple negative breast cancer

PURPOSE: No clinically useful target molecule has been identified for triple-negative (TN) breast cancer, i.e., estrogen receptor-negative, progesterone receptor-negative, human epidermal growth factor receptor-2-negative phenotype, and its prognosis is poor. The aim of this study is to clarify the...

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Autores principales: Ryu, Dong Won, Jung, Min Jung, Choi, Woo Sik, Lee, Chung Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Surgical Society 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3204700/
https://www.ncbi.nlm.nih.gov/pubmed/22066052
http://dx.doi.org/10.4174/jkss.2011.80.5.301
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author Ryu, Dong Won
Jung, Min Jung
Choi, Woo Sik
Lee, Chung Han
author_facet Ryu, Dong Won
Jung, Min Jung
Choi, Woo Sik
Lee, Chung Han
author_sort Ryu, Dong Won
collection PubMed
description PURPOSE: No clinically useful target molecule has been identified for triple-negative (TN) breast cancer, i.e., estrogen receptor-negative, progesterone receptor-negative, human epidermal growth factor receptor-2-negative phenotype, and its prognosis is poor. The aim of this study is to clarify the clinical and pathologic characteristics of triple negative breast cancer (TNBC). METHODS: The study subjects, 87 women with TNBC, were a subset of patients operated at Kosin University Gospel Hospital from January 2000 to December 2005. We examined pathologic characteristics such as tumor necrosis, infiltrating border, lymphocytic infiltration, prominent nucleoli in TNBC. And we studied the correlation between TNBC and several factors related to pathologic morphology. Chi-squared tests were used for statistical analysis. Kaplan-Meier estimates are presented for the survival function, and differences in survival were analyzed using the log rank test. RESULTS: Tumor necrosis was found in 51 patients (58.3%) in TNBC. And infiltrating border was found in 71 patients (81.0%). Also continuous lymphocytic distribution and prominent nucleoli was found in 31 patients (35.7%), 52 patients (59.7%), respectively. No association was detected between pathologic characteristics and other biological markers. Patients with tumor necrosis positive for TNBC didn't show shorter disease-free survival (P = 0.4490) or overall survival (P = 0.979) than patients without tumor necrosis. CONCLUSION: These findings suggest that pathologic characteristics cannot be used to classify triple-negative breast cancer into only two subtypes with differing prognoses. But because our study is small size study, more abundant patients' dates will be needed to evaluate the morphologic characteristics' predictive role.
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spelling pubmed-32047002011-11-07 Clinical significance of morphologic characteristics in triple negative breast cancer Ryu, Dong Won Jung, Min Jung Choi, Woo Sik Lee, Chung Han J Korean Surg Soc Original Article PURPOSE: No clinically useful target molecule has been identified for triple-negative (TN) breast cancer, i.e., estrogen receptor-negative, progesterone receptor-negative, human epidermal growth factor receptor-2-negative phenotype, and its prognosis is poor. The aim of this study is to clarify the clinical and pathologic characteristics of triple negative breast cancer (TNBC). METHODS: The study subjects, 87 women with TNBC, were a subset of patients operated at Kosin University Gospel Hospital from January 2000 to December 2005. We examined pathologic characteristics such as tumor necrosis, infiltrating border, lymphocytic infiltration, prominent nucleoli in TNBC. And we studied the correlation between TNBC and several factors related to pathologic morphology. Chi-squared tests were used for statistical analysis. Kaplan-Meier estimates are presented for the survival function, and differences in survival were analyzed using the log rank test. RESULTS: Tumor necrosis was found in 51 patients (58.3%) in TNBC. And infiltrating border was found in 71 patients (81.0%). Also continuous lymphocytic distribution and prominent nucleoli was found in 31 patients (35.7%), 52 patients (59.7%), respectively. No association was detected between pathologic characteristics and other biological markers. Patients with tumor necrosis positive for TNBC didn't show shorter disease-free survival (P = 0.4490) or overall survival (P = 0.979) than patients without tumor necrosis. CONCLUSION: These findings suggest that pathologic characteristics cannot be used to classify triple-negative breast cancer into only two subtypes with differing prognoses. But because our study is small size study, more abundant patients' dates will be needed to evaluate the morphologic characteristics' predictive role. The Korean Surgical Society 2011-05 2011-05-06 /pmc/articles/PMC3204700/ /pubmed/22066052 http://dx.doi.org/10.4174/jkss.2011.80.5.301 Text en Copyright © 2011, the Korean Surgical Society http://creativecommons.org/licenses/by-nc/3.0 Journal of the Korean Surgical Society is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ryu, Dong Won
Jung, Min Jung
Choi, Woo Sik
Lee, Chung Han
Clinical significance of morphologic characteristics in triple negative breast cancer
title Clinical significance of morphologic characteristics in triple negative breast cancer
title_full Clinical significance of morphologic characteristics in triple negative breast cancer
title_fullStr Clinical significance of morphologic characteristics in triple negative breast cancer
title_full_unstemmed Clinical significance of morphologic characteristics in triple negative breast cancer
title_short Clinical significance of morphologic characteristics in triple negative breast cancer
title_sort clinical significance of morphologic characteristics in triple negative breast cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3204700/
https://www.ncbi.nlm.nih.gov/pubmed/22066052
http://dx.doi.org/10.4174/jkss.2011.80.5.301
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