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Second primary malignancies in patients with male breast cancer

  • K. Hemminki
  • , G. Scélo
  • , P. Boffetta
  • , L. Mellemkjaer
  • , E. Tracey
  • , A. Andersen
  • , D. H. Brewster
  • , E. Pukkala
  • , M. McBride
  • , E. V. Kliewer
  • , K. S. Chia
  • , V. Pompe-Kirn
  • , C. Martos
  • , J. G. Jonasson
  • , X. Li
  • , P. Brennan

Rannsóknarafurð: Framlag til fræðitímaritsGreinritrýni

Útdráttur

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.

Upprunalegt tungumálEnska
Síður (frá-til)1288-1292
Síðufjöldi5
FræðitímaritBritish Journal of Cancer
Bindi92
Númer tölublaðs7
DOI
ÚtgáfustaðaÚtgefið - 11 apr. 2005

Athugasemd

Funding Information: We acknowledge the work of Didier Colin, IARC, for initial preparation of the data set. The analysis was supported by a R03 grant to IARC by the US NCI.

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