Triple-Negative Breast Cancer Risk Factors
Researchers are still learning why some women are more likely than others to develop triple-negative breast cancer. Research suggests that genes, age, race and ethnicity are risk factors.
Everyone has BRCA1 and BRCA2 genes, which we get from our mother and father. When they work properly, these genes prevent the development of cancers. But a small percentage of people with breast cancer are born with a mutation, or error, in BRCA1 or BRCA2.
If you are born with a BRCA1 or BRCA2 gene mutation, you are at increased risk for developing breast, ovarian and other cancers throughout your life. The BRCA1 mutation puts you at higher risk for developing a basal-like breast cancer, such as triple-negative breast cancer. Scientists are still trying to find out why.
Keep in mind, not all breast cancers from BRCA mutations are triple-negative. In fact, BRCA2 mutations are more likely to be present in estrogen receptor-positive breast cancers.
If you have a family history of breast cancer, you and your relatives could carry a BRCA1 or BRCA2 mutation. You could also be the first person in your family known to develop breast cancer because of a BRCA mutation. Knowing your BRCA status can help you and your doctors discuss an effective treatment plan and learn ways to reduce your risk for recurrence. A genetic counselor can talk with you about genetic testing.
Studies suggest that being premenopausal, African-American or Caribbean increases your risk of developing basal-like or triple-negative breast cancer. Among African-American women who develop breast cancer, there is an estimated 20 to 40 percent chance of the breast cancer being triple-negative.
Researchers don’t yet understand why premenopausal women (who tend to be younger), and women in some ethnic groups have higher rates of triple-negative breast cancer than other groups of women.