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. 2021 Nov 29;59(7):632–643. doi: 10.1136/jmedgenet-2021-107904

Table 1.

Summary of components of the EOC risk model

RF group RF category Comments
FH Explicit FH of ovarian and other cancers (breast, prostate, male breast and pancreatic) Considers families of arbitrary size and structure, including affected and unaffected relatives
Sex Sex of all family members
Age Ages at cancer diagnosis or current ages/age at death of family members
Genetic factors
 Rare truncating/pathogenic variants BRCA1
BRCA2
RAD51D
RAD51C
BRIP1
 Common genetic variants Polygenic Risk Score Explaining 5% of the polygenic variance
 Unobserved genetic effects Residual polygenic component Accounts for the residual familial aggregation of EOC
Lifestyle/hormonal/reproductive
Height Measured in cm (five categories)
Body Mass Index Measured in kg/m2 (three categories)
Parity Number of live births (three categories)
Endometriosis Yes/no
Use of oral contraception Years of use (five categories)
Use of hormone replacement therapy Never/ever
Tubal ligation Yes/no
Breast tumour pathology Oestrogen, progesterone, HER2 receptor, CK14, CK5/6 status As implemented in the BOADICEA breast cancer model
Demographic factors
 Country of origin Country Defines the underlying incidences used
 Birth cohort Defined by the person’s year of birth Eight calendar year-specific sets of incidences
 Family ethnicity Ashkenazi Jewish origin

BOADICEA, Breast and Ovarian Analysis of Disease Incidence and Carrier Estimation Algorithm; EOC, epithelial tubo-ovarian cancer; FH, family history; RF, risk factor.