Journal article
Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer
AK Win, SP Cleary, JG Dowty, JA Baron, JP Young, DD Buchanan, MC Southey, T Burnett, PS Parfrey, RC Green, LL Marchand, PA Newcomb, RW Haile, NM Lindor, JL Hopper, S Gallinger, MA Jenkins
International Journal of Cancer | WILEY | Published : 2011
DOI: 10.1002/ijc.25870
Abstract
Cancer risks for a person who has inherited a MUTYH mutation from only one parent (monoallelic mutation carrier) are uncertain. Using the Colon Cancer Family Registry and Newfoundland Familial Colon Cancer Registry, we identified 2,179 first- and second-degree relatives of 144 incident colorectal cancer (CRC) cases who were monoallelic or biallelic mutation carriers ascertained by sampling population complete cancer registries in the United States, Canada and Australia. Using Cox regression weighted to adjust for sampling on family history, we estimated that the country-, age- and sex-specific standardized incidence ratios (SIRs) for monoallelic mutation carriers, compared to the general pop..
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Awarded by National Cancer Institute
Funding Acknowledgements
Grant sponsor: National Cancer Institute, National Institutes of Health; Grant number: RFA #CA-95-011; Grant sponsor: Canadian Institute of Health Sciences (Interdisciplinary Research Team on Colorectal Cancer); Grant number: CIHR-CPT79845