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Age- and Tumor Subtype–Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers
- Schmidt, Marjanka K;
- Hogervorst, Frans;
- van Hien, Richard;
- Cornelissen, Sten;
- Broeks, Annegien;
- Adank, Muriel A;
- Meijers, Hanne;
- Waisfisz, Quinten;
- Hollestelle, Antoinette;
- Schutte, Mieke;
- van den Ouweland, Ans;
- Hooning, Maartje;
- Andrulis, Irene L;
- Anton-Culver, Hoda;
- Antonenkova, Natalia N;
- Antoniou, Antonis C;
- Arndt, Volker;
- Bermisheva, Marina;
- Bogdanova, Natalia V;
- Bolla, Manjeet K;
- Brauch, Hiltrud;
- Brenner, Hermann;
- Brüning, Thomas;
- Burwinkel, Barbara;
- Chang-Claude, Jenny;
- Chenevix-Trench, Georgia;
- Couch, Fergus J;
- Cox, Angela;
- Cross, Simon S;
- Czene, Kamila;
- Dunning, Alison M;
- Fasching, Peter A;
- Figueroa, Jonine;
- Fletcher, Olivia;
- Flyger, Henrik;
- Galle, Eva;
- García-Closas, Montserrat;
- Giles, Graham G;
- Haeberle, Lothar;
- Hall, Per;
- Hillemanns, Peter;
- Hopper, John L;
- Jakubowska, Anna;
- John, Esther M;
- Jones, Michael;
- Khusnutdinova, Elza;
- Knight, Julia A;
- Kosma, Veli-Matti;
- Kristensen, Vessela;
- Lee, Andrew;
- Lindblom, Annika;
- Lubinski, Jan;
- Mannermaa, Arto;
- Margolin, Sara;
- Meindl, Alfons;
- Milne, Roger L;
- Muranen, Taru A;
- Newcomb, Polly A;
- Offit, Kenneth;
- Park-Simon, Tjoung-Won;
- Peto, Julian;
- Pharoah, Paul DP;
- Robson, Mark;
- Rudolph, Anja;
- Sawyer, Elinor J;
- Schmutzler, Rita K;
- Seynaeve, Caroline;
- Soens, Julie;
- Southey, Melissa C;
- Spurdle, Amanda B;
- Surowy, Harald;
- Swerdlow, Anthony;
- Tollenaar, Rob AEM;
- Tomlinson, Ian;
- Trentham-Dietz, Amy;
- Vachon, Celine;
- Wang, Qin;
- Whittemore, Alice S;
- Ziogas, Argyrios;
- van der Kolk, Lizet;
- Nevanlinna, Heli;
- Dörk, Thilo;
- Bojesen, Stig;
- Easton, Douglas F
- et al.
Published Web Location
https://doi.org/10.1200/jco.2016.66.5844Abstract
Purpose
CHEK2*1100delC is a well-established breast cancer risk variant that is most prevalent in European populations; however, there are limited data on risk of breast cancer by age and tumor subtype, which limits its usefulness in breast cancer risk prediction. We aimed to generate tumor subtype- and age-specific risk estimates by using data from the Breast Cancer Association Consortium, including 44,777 patients with breast cancer and 42,997 controls from 33 studies genotyped for CHEK2*1100delC.Patients and methods
CHEK2*1100delC genotyping was mostly done by a custom Taqman assay. Breast cancer odds ratios (ORs) for CHEK2*1100delC carriers versus noncarriers were estimated by using logistic regression and adjusted for study (categorical) and age. Main analyses included patients with invasive breast cancer from population- and hospital-based studies.Results
Proportions of heterozygous CHEK2*1100delC carriers in controls, in patients with breast cancer from population- and hospital-based studies, and in patients with breast cancer from familial- and clinical genetics center-based studies were 0.5%, 1.3%, and 3.0%, respectively. The estimated OR for invasive breast cancer was 2.26 (95%CI, 1.90 to 2.69; P = 2.3 × 10(-20)). The OR was higher for estrogen receptor (ER)-positive disease (2.55 [95%CI, 2.10 to 3.10; P = 4.9 × 10(-21)]) than it was for ER-negative disease (1.32 [95%CI, 0.93 to 1.88; P = .12]; P interaction = 9.9 × 10(-4)). The OR significantly declined with attained age for breast cancer overall (P = .001) and for ER-positive tumors (P = .001). Estimated cumulative risks for development of ER-positive and ER-negative tumors by age 80 in CHEK2*1100delC carriers were 20% and 3%, respectively, compared with 9% and 2%, respectively, in the general population of the United Kingdom.Conclusion
These CHEK2*1100delC breast cancer risk estimates provide a basis for incorporating CHEK2*1100delC into breast cancer risk prediction models and into guidelines for intensified screening and follow-up.Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.
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