Breast Cancer, Ovarian Cancer
Conditions
Brief summary
1. To evaluate the prevalence of BRCA1/2 mutation of breast cancer patients with family history of breast/ovarian cancer. 2. To evaluate the prevalence of BRCA1/2 mutation of breast cancer patients without family history, but high risk of hereditary cancer. 3. To evaluate the prevalence of BRCA1/2 mutation of family member of BRCA1/2 mutation. 4. To evaluate the prevalence of ovarian cancer of population of above 3 groups.
Detailed description
1. To find founder mutation in Korean 2. To correlation prevalence with risk evaluation 3. To find risk factors concerning life style
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Over 19 years old * Agree to this study * Breast cancer patient with family history of breast/ovarian cancer (1 subgroup) * Breast cancer patient; young age (\<40), bilateral, male, combined ovarian (2 subgroup) * Family members with 1, 2 subgroups (3 subgroup)
Exclusion criteria
* Under 20 years old * Unable to decide for oneself
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Find out the prevalence of BRCA1/2 mutation of high risk breast cancer patients | 6 years |
Countries
South Korea