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Clinicopathologic characteristics and prognosis for male breast cancer compared to female breast cancer

Male breast cancer (MBC) is rare. Due to limited information, MBC has always been understudied. We conducted a retrospective population-based cohort study using data from the National Cancer Institute’s Surveillance, Epidemiology, and End Results (SEER) program. The clinical and biological features...

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Autores principales: Yao, Nan, Shi, Wenzai, Liu, Tong, Siyin, Sarah Tan, Wang, Weiqi, Duan, Ning, Xu, Guoshuai, Qu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741943/
https://www.ncbi.nlm.nih.gov/pubmed/34997151
http://dx.doi.org/10.1038/s41598-021-04342-0
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author Yao, Nan
Shi, Wenzai
Liu, Tong
Siyin, Sarah Tan
Wang, Weiqi
Duan, Ning
Xu, Guoshuai
Qu, Jun
author_facet Yao, Nan
Shi, Wenzai
Liu, Tong
Siyin, Sarah Tan
Wang, Weiqi
Duan, Ning
Xu, Guoshuai
Qu, Jun
author_sort Yao, Nan
collection PubMed
description Male breast cancer (MBC) is rare. Due to limited information, MBC has always been understudied. We conducted a retrospective population-based cohort study using data from the National Cancer Institute’s Surveillance, Epidemiology, and End Results (SEER) program. The clinical and biological features of female breast cancer (FBC) patients were compared with MBC patients. Cox regression models and competing risks analyses were used to identify risk factors associated with cancer-related survival in MBC and FBC groups. Results showed that MBC patients suffered from higher TNM stages, tumor grades, and a higher percentage of hormone receptor-positive tumors, compared with FBC patients (all p < 0.05). In addition, the breast tumor locations varied a lot between males and females (p < 0.05). FBC patients were associated with superior overall survival than MBC patients. Results from multivariate cox regression and competing risks analyses showed age, race, T, N, M-stages, tumor grades, estrogen receptor (ER)/progesterone receptor (PR) and human epidermal growth factor receptor-2 (HER-2) overexpression were independent prognosis factors in FBC patients (all p < 0.05). MBC patients had similar risk factors to FBC patients, but PR and HER-2 status did not independently influence survival (all p > 0.05). Tumor location was an independent prognostic factor for both gender groups.
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spelling pubmed-87419432022-01-10 Clinicopathologic characteristics and prognosis for male breast cancer compared to female breast cancer Yao, Nan Shi, Wenzai Liu, Tong Siyin, Sarah Tan Wang, Weiqi Duan, Ning Xu, Guoshuai Qu, Jun Sci Rep Article Male breast cancer (MBC) is rare. Due to limited information, MBC has always been understudied. We conducted a retrospective population-based cohort study using data from the National Cancer Institute’s Surveillance, Epidemiology, and End Results (SEER) program. The clinical and biological features of female breast cancer (FBC) patients were compared with MBC patients. Cox regression models and competing risks analyses were used to identify risk factors associated with cancer-related survival in MBC and FBC groups. Results showed that MBC patients suffered from higher TNM stages, tumor grades, and a higher percentage of hormone receptor-positive tumors, compared with FBC patients (all p < 0.05). In addition, the breast tumor locations varied a lot between males and females (p < 0.05). FBC patients were associated with superior overall survival than MBC patients. Results from multivariate cox regression and competing risks analyses showed age, race, T, N, M-stages, tumor grades, estrogen receptor (ER)/progesterone receptor (PR) and human epidermal growth factor receptor-2 (HER-2) overexpression were independent prognosis factors in FBC patients (all p < 0.05). MBC patients had similar risk factors to FBC patients, but PR and HER-2 status did not independently influence survival (all p > 0.05). Tumor location was an independent prognostic factor for both gender groups. Nature Publishing Group UK 2022-01-07 /pmc/articles/PMC8741943/ /pubmed/34997151 http://dx.doi.org/10.1038/s41598-021-04342-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yao, Nan
Shi, Wenzai
Liu, Tong
Siyin, Sarah Tan
Wang, Weiqi
Duan, Ning
Xu, Guoshuai
Qu, Jun
Clinicopathologic characteristics and prognosis for male breast cancer compared to female breast cancer
title Clinicopathologic characteristics and prognosis for male breast cancer compared to female breast cancer
title_full Clinicopathologic characteristics and prognosis for male breast cancer compared to female breast cancer
title_fullStr Clinicopathologic characteristics and prognosis for male breast cancer compared to female breast cancer
title_full_unstemmed Clinicopathologic characteristics and prognosis for male breast cancer compared to female breast cancer
title_short Clinicopathologic characteristics and prognosis for male breast cancer compared to female breast cancer
title_sort clinicopathologic characteristics and prognosis for male breast cancer compared to female breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741943/
https://www.ncbi.nlm.nih.gov/pubmed/34997151
http://dx.doi.org/10.1038/s41598-021-04342-0
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