Enhancing the BOADICEA cancer risk prediction model to incorporate new data onRAD51C,RAD51D,BARD1updates to tumour pathology and cancer incidence

Author:

Lee AndrewORCID,Mavaddat Nasim,Cunningham Alex,Carver Tim,Ficorella Lorenzo,Archer Stephanie,Walter Fiona M,Tischkowitz Marc,Roberts Jonathan,Usher-Smith Juliet,Simard Jacques,Schmidt Marjanka K,Devilee PeterORCID,Zadnik Vesna,Jürgens Hannes,Mouret-Fourme Emmanuelle,De Pauw Antoine,Rookus Matti,Mooij Thea M,Pharoah Paul PDORCID,Easton Douglas F,Antoniou Antonis CORCID

Abstract

BackgroundBOADICEA (Breast and Ovarian Analysis of Disease Incidence and Carrier Estimation Algorithm) for breast cancer and the epithelial tubo-ovarian cancer (EOC) models included in the CanRisk tool (www.canrisk.org) provide future cancer risks based on pathogenic variants in cancer-susceptibility genes, polygenic risk scores, breast density, questionnaire-based risk factors and family history. Here, we extend the models to include the effects of pathogenic variants in recently established breast cancer and EOC susceptibility genes, up-to-date age-specific pathology distributions and continuous risk factors.MethodsBOADICEA was extended to further incorporate the associations of pathogenic variants inBARD1,RAD51CandRAD51Dwith breast cancer risk. The EOC model was extended to include the association ofPALB2pathogenic variants with EOC risk. Age-specific distributions of oestrogen-receptor-negative and triple-negative breast cancer status for pathogenic variant carriers in these genes andCHEK2andATMwere also incorporated. A novel method to include continuous risk factors was developed, exemplified by including adult height as continuous.ResultsBARD1,RAD51CandRAD51Dexplain 0.31% of the breast cancer polygenic variance. When incorporated into the multifactorial model, 34%–44% of these carriers would be reclassified to the near-population and 15%–22% to the high-risk categories based on the UK National Institute for Health and Care Excellence guidelines. Under the EOC multifactorial model, 62%, 35% and 3% ofPALB2carriers have lifetime EOC risks of <5%, 5%–10% and >10%, respectively. Including height as continuous, increased the breast cancer relative risk variance from 0.002 to 0.010.ConclusionsThese extensions will allow for better personalised risks forBARD1,RAD51C,RAD51DandPALB2pathogenic variant carriers and more informed choices on screening, prevention, risk factor modification or other risk-reducing options.

Funder

the Quebec Breast Cancer Foundation, the CHU de Quebec

Government of Canada

Canadian Institutes of Health Research

Cancer Research UK

European Union

NIHR Cambridge Biomedical Research Centre

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference46 articles.

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