Abstract:
:Breast cancer (BC) patients diagnosed between two screenings (interval cancers) are more likely than screen-detected patients to carry rare deleterious mutations in cancer genes potentially leading to increased risk for other non-breast cancer (non-BC) tumors. In this study, we include 14,846 women diagnosed with BC of which 1,772 are interval and 13,074 screen-detected. Compared to women with screen-detected cancers, interval breast cancer patients are more likely to have a non-BC tumor before (Odds ratio (OR): 1.43 [1.19-1.70], P = 9.4 x 10-5) and after (OR: 1.28 [1.14-1.44], P = 4.70 x 10-5) breast cancer diagnosis, are more likely to report a family history of non-BC tumors and have a lower genetic risk score based on common variants for non-BC tumors. In conclusion, interval breast cancer is associated with other tumors and common cancer variants are unlikely to be responsible for this association. These findings could have implications for future screening and prevention programs.
journal_name
Nat Communjournal_title
Nature communicationsauthors
Grassmann F,He W,Eriksson M,Gabrielson M,Hall P,Czene Kdoi
10.1038/s41467-019-12652-1subject
Has Abstractpub_date
2019-10-22 00:00:00pages
4648issue
1issn
2041-1723pii
10.1038/s41467-019-12652-1journal_volume
10pub_type
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