Risk of non-melanoma cancers in first-degree relatives of CDKN2A mutation carriers Journal Article


Authors: Mukherjee, B.; DeLancey, J. O.; Raskin, L.; Everett, J.; Jeter, J.; Begg, C. B.; Orlow, I.; Berwick, M.; Armstrong, B. K.; Kricker, A.; Marrett, L. D.; Millikan, R. C.; Culver, H. A.; Rosso, S.; Zanetti, R.; Kanetsky, P. A.; From, L.; Gruber, S. B.
Article Title: Risk of non-melanoma cancers in first-degree relatives of CDKN2A mutation carriers
Abstract: The purpose of this study was to quantify the risk of cancers other than melanoma among family members of CDKN2A mutation carriers using data from the Genes, Environment and Melanoma study. Relative risks (RRs) of all non-melanoma cancers among first-degree relatives (FDRs) of melanoma patients with CDKN2A mutations (n = 65) and FDRs of melanoma patients without mutations (n = 3537) were calculated as the ratio of estimated event rates (number of cancers/total person-years) in FDRs of carriers vs noncarriers with exact Clopper-Pearson-type tests and 95% confidence intervals (CIs). All statistical tests were two-sided. There were 56 (13.1%) non-melanoma cancers reported among 429 FDRs of mutation carriers and 2199 (9.4%) non-melanoma cancers in 23452 FDRs of noncarriers. The FDRs of carriers had an increased risk of any cancer other than melanoma (56 cancers among 429 FDRs of carrier probands vs 2199 cancers among 23452 FDRs of noncarrier probands; RR = 1.5, 95% CI = 1.2 to 2.0, P = .005), gastrointestinal cancer (20 cancers among 429 FDRs of carrier probands vs 506 cancers among 23452 FDRs of noncarrier probands; RR = 2.4, 95% CI = 1.4 to 3.7, P = .001), and pancreatic cancer (five cancers among 429 FDRs of carrier probands vs 41 cancers among 23452 FDRs of noncarrier probands; RR = 7.4, 95% CI = 2.3 to 18.7, P = .002). Wilms tumor was reported in two FDRs of carrier probands and three FDRs of noncarrier probands (RR = 40.4, 95% CI = 3.4 to 352.7, P = .005). The lifetime risk of any cancer other than melanoma among CDKN2A mutation carriers was estimated as 59.0% by age 85 years (95% CI = 39.0% to 75.4%) by the kin-cohort method, under the standard assumptions of Mendelian genetics on the genotype distribution of FDRs conditional on proband genotype. © 2012 The Author.
Keywords: controlled study; gene mutation; major clinical study; cancer localization; cancer risk; pancreas cancer; colorectal cancer; melanoma; breast cancer; genotype; lung cancer; heterozygote; risk factor; risk assessment; digestive system cancer; confidence interval; brain cancer; cyclin dependent kinase inhibitor 2a; relative; nephroblastoma; mendelian randomization analysis
Journal Title: JNCI: Journal of the National Cancer Institute
Volume: 104
Issue: 12
ISSN: 0027-8874
Publisher: Oxford University Press  
Date Published: 2012-06-20
Start Page: 953
End Page: 956
Language: English
DOI: 10.1093/jnci/djs221
PROVIDER: scopus
PMCID: PMC3379723
PUBMED: 22534780
DOI/URL:
Notes: --- - "Cited By (since 1996): 1" - "Export Date: 4 September 2012" - "CODEN: JNCIA" - "Source: Scopus"
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  1. Colin B Begg
    306 Begg
  2. Irene Orlow
    247 Orlow