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Second primary malignancies in patients with male breast cancer
An international multicentre study of first and second primary neoplasms associated with male breast cancer was carried out by pooling data from 13 cancer registries. Among a total of 3409 men with primary breast cancer, 426 (12.5%) developed a second neoplasia; other than breast cancer, a 34% overa...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361970/ https://www.ncbi.nlm.nih.gov/pubmed/15798766 http://dx.doi.org/10.1038/sj.bjc.6602505 |
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author | Hemminki, K Scélo, G Boffetta, P Mellemkjaer, L Tracey, E Andersen, A Brewster, D H Pukkala, E McBride, M Kliewer, E V Chia, K-S Pompe-Kirn, V Martos, C Jonasson, J G Li, X Brennan, P |
author_facet | Hemminki, K Scélo, G Boffetta, P Mellemkjaer, L Tracey, E Andersen, A Brewster, D H Pukkala, E McBride, M Kliewer, E V Chia, K-S Pompe-Kirn, V Martos, C Jonasson, J G Li, X Brennan, P |
author_sort | Hemminki, K |
collection | PubMed |
description | An international multicentre study of first and second primary neoplasms associated with male breast cancer was carried out by pooling data from 13 cancer registries. Among a total of 3409 men with primary breast cancer, 426 (12.5%) developed a second neoplasia; other than breast cancer, a 34% overall excess risk of second primary neoplasia, affecting the small intestine (standardised incidence ratio, 4.95, 95% confidence interval, 1.35–12.7), rectum (1.78, 1.20–2.54), pancreas (1.93, 1.14–3.05), skin (nonmelanoma, 1.65, 1.16–2.29), prostate (1.61, 1.34–1.93) and lymphohaematopoietic system (1.63, 1.12–2.29). A total of 225 male breast cancers was recorded after cancers other than breast cancer, but an increase was found only after lymphohaematopoietic neoplasms. BRCA2 (and to some extent BRCA1) mutations may explain the findings for pancreatic and prostate cancers. Increases at other sites may be related to unknown factors or to chance. This large study shows that the risks for second discordant tumours after male breast cancer pose only a moderate excess risk. |
format | Text |
id | pubmed-2361970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23619702009-09-10 Second primary malignancies in patients with male breast cancer Hemminki, K Scélo, G Boffetta, P Mellemkjaer, L Tracey, E Andersen, A Brewster, D H Pukkala, E McBride, M Kliewer, E V Chia, K-S Pompe-Kirn, V Martos, C Jonasson, J G Li, X Brennan, P Br J Cancer Epidemiology An international multicentre study of first and second primary neoplasms associated with male breast cancer was carried out by pooling data from 13 cancer registries. Among a total of 3409 men with primary breast cancer, 426 (12.5%) developed a second neoplasia; other than breast cancer, a 34% overall excess risk of second primary neoplasia, affecting the small intestine (standardised incidence ratio, 4.95, 95% confidence interval, 1.35–12.7), rectum (1.78, 1.20–2.54), pancreas (1.93, 1.14–3.05), skin (nonmelanoma, 1.65, 1.16–2.29), prostate (1.61, 1.34–1.93) and lymphohaematopoietic system (1.63, 1.12–2.29). A total of 225 male breast cancers was recorded after cancers other than breast cancer, but an increase was found only after lymphohaematopoietic neoplasms. BRCA2 (and to some extent BRCA1) mutations may explain the findings for pancreatic and prostate cancers. Increases at other sites may be related to unknown factors or to chance. This large study shows that the risks for second discordant tumours after male breast cancer pose only a moderate excess risk. Nature Publishing Group 2005-04-11 2005-03-29 /pmc/articles/PMC2361970/ /pubmed/15798766 http://dx.doi.org/10.1038/sj.bjc.6602505 Text en Copyright © 2005 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Epidemiology Hemminki, K Scélo, G Boffetta, P Mellemkjaer, L Tracey, E Andersen, A Brewster, D H Pukkala, E McBride, M Kliewer, E V Chia, K-S Pompe-Kirn, V Martos, C Jonasson, J G Li, X Brennan, P Second primary malignancies in patients with male breast cancer |
title | Second primary malignancies in patients with male breast cancer |
title_full | Second primary malignancies in patients with male breast cancer |
title_fullStr | Second primary malignancies in patients with male breast cancer |
title_full_unstemmed | Second primary malignancies in patients with male breast cancer |
title_short | Second primary malignancies in patients with male breast cancer |
title_sort | second primary malignancies in patients with male breast cancer |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361970/ https://www.ncbi.nlm.nih.gov/pubmed/15798766 http://dx.doi.org/10.1038/sj.bjc.6602505 |
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