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Clinicopathological characteristics and survival outcomes of male breast cancer according to race: A SEER population-based study
To investigate the clinicopathological characteristics and survival outcomes of breast cancer in the male population, 8,607 cases of patients were identified in the Surveillance, Epidemiology, and End Results (SEER) database, including white males (n = 7122), black males (n = 1111), and other males...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642508/ https://www.ncbi.nlm.nih.gov/pubmed/29050233 http://dx.doi.org/10.18632/oncotarget.18265 |
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author | Sun, He-Fen Zhao, Yang Gao, Shui-Ping Li, Liang-Dong Fu, Wen-Yan Jiang, Hong-lin Chen, Meng-Ting Yang, Li-Peng Jin, Wei |
author_facet | Sun, He-Fen Zhao, Yang Gao, Shui-Ping Li, Liang-Dong Fu, Wen-Yan Jiang, Hong-lin Chen, Meng-Ting Yang, Li-Peng Jin, Wei |
author_sort | Sun, He-Fen |
collection | PubMed |
description | To investigate the clinicopathological characteristics and survival outcomes of breast cancer in the male population, 8,607 cases of patients were identified in the Surveillance, Epidemiology, and End Results (SEER) database, including white males (n = 7122), black males (n = 1111), and other males (American Indian/AK Native, Asian/Pacific Islander) (n = 374). Black male breast cancer patients were more likely to be in stages II–IV and have more advanced tumors. The rate of lymph node (LN) involvement at diagnosis was higher in black men than in whites and others. The ER- and PR-positive rates were lower in black men than in whites and others. The distant metastasis rate was higher in blacks than in whites and others. Furthermore, the overall survival (OR) rates and breast cancer-specific survival rates were significantly poorer in blacks than in whites and others (χ(2) = 29.974, P < 0.001; χ(2) = 7.285, P = 0.026, respectively). In a multivariate analysis, the results showed that race could also be a prognostic indicator (P < 0.001). Moreover, significant differences were also observed in OS among 1:1:1 matched white, black, and other groups (P < 0.001). Differences in outcomes may be partially explained by differences in tumor grades, LN status, and ER and PR status between the 3 groups. This study might provide insights into a better understanding of male breast cancer. |
format | Online Article Text |
id | pubmed-5642508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56425082017-10-18 Clinicopathological characteristics and survival outcomes of male breast cancer according to race: A SEER population-based study Sun, He-Fen Zhao, Yang Gao, Shui-Ping Li, Liang-Dong Fu, Wen-Yan Jiang, Hong-lin Chen, Meng-Ting Yang, Li-Peng Jin, Wei Oncotarget Research Paper To investigate the clinicopathological characteristics and survival outcomes of breast cancer in the male population, 8,607 cases of patients were identified in the Surveillance, Epidemiology, and End Results (SEER) database, including white males (n = 7122), black males (n = 1111), and other males (American Indian/AK Native, Asian/Pacific Islander) (n = 374). Black male breast cancer patients were more likely to be in stages II–IV and have more advanced tumors. The rate of lymph node (LN) involvement at diagnosis was higher in black men than in whites and others. The ER- and PR-positive rates were lower in black men than in whites and others. The distant metastasis rate was higher in blacks than in whites and others. Furthermore, the overall survival (OR) rates and breast cancer-specific survival rates were significantly poorer in blacks than in whites and others (χ(2) = 29.974, P < 0.001; χ(2) = 7.285, P = 0.026, respectively). In a multivariate analysis, the results showed that race could also be a prognostic indicator (P < 0.001). Moreover, significant differences were also observed in OS among 1:1:1 matched white, black, and other groups (P < 0.001). Differences in outcomes may be partially explained by differences in tumor grades, LN status, and ER and PR status between the 3 groups. This study might provide insights into a better understanding of male breast cancer. Impact Journals LLC 2017-05-26 /pmc/articles/PMC5642508/ /pubmed/29050233 http://dx.doi.org/10.18632/oncotarget.18265 Text en Copyright: © 2017 Sun et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Sun, He-Fen Zhao, Yang Gao, Shui-Ping Li, Liang-Dong Fu, Wen-Yan Jiang, Hong-lin Chen, Meng-Ting Yang, Li-Peng Jin, Wei Clinicopathological characteristics and survival outcomes of male breast cancer according to race: A SEER population-based study |
title | Clinicopathological characteristics and survival outcomes of male breast cancer according to race: A SEER population-based study |
title_full | Clinicopathological characteristics and survival outcomes of male breast cancer according to race: A SEER population-based study |
title_fullStr | Clinicopathological characteristics and survival outcomes of male breast cancer according to race: A SEER population-based study |
title_full_unstemmed | Clinicopathological characteristics and survival outcomes of male breast cancer according to race: A SEER population-based study |
title_short | Clinicopathological characteristics and survival outcomes of male breast cancer according to race: A SEER population-based study |
title_sort | clinicopathological characteristics and survival outcomes of male breast cancer according to race: a seer population-based study |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642508/ https://www.ncbi.nlm.nih.gov/pubmed/29050233 http://dx.doi.org/10.18632/oncotarget.18265 |
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