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. It is well established that women with a first primary breast cancer run a 2 -5-fold increased risk of developing second primary breast cancer compared with the risk for the first primary breast cancer (Chen et al, 1999;Vaittinen and Hemminki, 2000). In men, the risk of second breast cancer after a first breast cancer is much higher, of the order of 100 (Dong and Hemminki, 2001;Auvinen et al, 2002), despite the overall pathology, natural history and hormonal risk factors for sporadic and familial breast cancers showing certain similarities for both genders; socioeconomic risk factors also appear similar for male and female breast cancers (Hsing et al, 1998;Hemminki and Li, 2003;Hemminki et al, 2003b). Klinefelter syndrome, gynaecomastia and testicular disease are additional male risk factors (Hultborn et al, 1997;Lynch et al, 1999). Heritable mutations predisposing to male breast cancer include BRCA2, BRCA1 and, possibly, the androgen receptor gene (Lynch et al, 1999;Liede et al, 2004). Accounting for some 15% of all cases, BRCA2 mutations are the most common heritable factors in male breast cancer, and, in addition to breast cancer, carriers have an increased risk of prostate, pancreatic and stomach cancers and melanomas (Liede et al, 2004). BRCA1 mutations are less common in male than female breast cancer, and also affect prostate cancer (Liede et al, 2004). Few studies have assessed the risk of second cancers, other than breast cancer, among male breast cancer patients and melanoma appears to the be the only tumour showing an excess among men (Auvinen et al, 2002;Hemminki and Granstrom, 2002).In the present study, the risks of second primary neoplasms for first male breast cancer, and for male breast cancer following any other cancer are based on pooled data from 13 large cancer registries, which are collaborating in studies on second primary neoplasms. As a result, the study is two times larger than the previous largest study (Auvinen et al, 20...