A simple tool for identifying unaffected women at a moderately increased or potentially high risk of breast cancer based on their family history

Breast. 2003 Apr;12(2):120-7. doi: 10.1016/s0960-9776(02)00285-0.

Abstract

Family history of breast cancer is a more important aspect of clinical management following the discovery of the genes BRCA1 and BRCA2. The authors developed a short questionnaire to categorize risk according to breast cancer history in close relatives. It was completed by 559 women attending for screening mammograms in Sydney, Australia. Twenty-three per cent reported a family history sufficient to be classified at a moderately increased or potentially high risk according to national guidelines (category II or III). Only 29 women (5%) made errors such that their risk category could not be determined. Validation of responses from 89 women, 44 from category II or III, found 100% agreement with classification after interview by a genetic counsellor. This questionnaire has the potential to accurately triage risk based on a woman's knowledge of her family history, and could be used in a variety of settings to identify women who may require further assessment, management and referral advice.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Australia / epidemiology
  • Breast Neoplasms / diagnosis
  • Breast Neoplasms / epidemiology*
  • Breast Neoplasms / genetics*
  • Female
  • Genetic Predisposition to Disease* / epidemiology*
  • Genetic Testing / methods
  • Humans
  • Incidence
  • Mammography / methods
  • Mass Screening / methods*
  • Middle Aged
  • Population Surveillance
  • Reproducibility of Results
  • Risk Assessment
  • Sensitivity and Specificity
  • Surveys and Questionnaires*