Second primary malignancies in patients with male breast cancer

被引:43
|
作者
Hemminki, K
Scélo, G
Boffetta, P
Mellemkjaer, L
Tracey, E
Andersen, A
Brewster, DH
Pukkala, E
McBride, M
Kliewer, EV
Chia, KS
Pompe-Kirn, V
Martos, C
Jonasson, JG
Li, X
Brennan, P
机构
[1] German Canc Res Ctr, Div Mol Genet Epidemiol, D-69120 Heidelberg, Germany
[2] Karolinska Inst, Novum, Dept Biosci, Huddinge, Sweden
[3] Int Agcy Res Canc, F-69372 Lyon, France
[4] Danish Canc Soc, Inst Canc Epidemiol, Copenhagen, Denmark
[5] Cent Canc Registry, Woolloomooloo, NSW, Australia
[6] Canc Registry Norway, Oslo, Norway
[7] NHS Natl Serv Scotland, Informat Serv, Scottish Canc Registry, Edinburgh, Midlothian, Scotland
[8] Finnish Canc Registry, Inst Stat & Epidemiol Canc Res, FIN-00170 Helsinki, Finland
[9] British Columbia Canc Registry, Canc Control Res Programme, Vancouver, BC, Canada
[10] CancerCare Manitoba, Epidemiol & Canc Registry, Winnipeg, MB, Canada
[11] Univ Manitoba, Winnipeg, MB, Canada
[12] Singapore Canc Registry, Singapore, Singapore
[13] Inst Oncol, Canc Registry Slovenia, Ljubljana, Slovenia
[14] Hlth Dept Aragon Govt, Canc Registry Zaragoza, Zaragoza, Spain
[15] Iceland Canc Soc, Iceland Canc Registry, Reykjavik, Iceland
[16] Univ Iceland, Fac Med, Reykjavik, Iceland
关键词
subsequent malignancy; cancer registry; pooled analysis; BRCA in men; discordant sites;
D O I
10.1038/sj.bjc.6602505
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1288 / 1292
页数:5
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