Everyone has BRCA1 and BRCA2 genes. These genes help repair damage to DNA within cells. However, some individuals inherit a mutation, or error, in one of their BRCA genes, which increases their risk for certain cancers, including breast (female and male), ovarian, pancreatic and prostate cancers, as well as melanoma. There are options available to reduce and manage these cancer risks.
Women and men of Ashkenazi Jewish (Central or Eastern European) ancestry have a 1 in 40 chance of carrying a BRCA1 or BRCA2 gene mutation. This is about a five times greater chance than that of the general population. Many Ashkenazi Jewish women and men are not aware that they have a BRCA gene mutation. A personal and/or family history of breast, ovarian, high-grade prostate or pancreatic cancers on your mother’s or father’s side of the family may be a sign of a hereditary gene mutation. Men and women can inherit a BRCA gene mutation from their mother or father.
Women who have a BRCA gene mutation have up to a 75% lifetime risk of developing breast cancer and up to a 50% lifetime risk of developing ovarian cancer. A personalized cancer risk management plan for women can include increased and earlier screenings (such as breast MRI and mammogram), consideration of risk-reducing surgeries, and chemoprevention. (taking a medication shown to lower the chance of developing cancer).
Men can also have BRCA1 and BRCA2 gene mutations and can be at increased risk for certain cancers. While cancer risks in male BRCA carriers are not as dramatically elevated as those of female BRCA carriers, cancer risk management and early detection are crucial. Medical management for men with a BRCA mutation may include clinical breast exams, mammograms and earlier prostate cancer screenings.
In patients already diagnosed with cancer, knowing about a BRCA mutation may provide the opportunity for novel therapies or clinical trials.
FREQUENTLY ASKED QUESTIONS ABOUT BRCA
Who should consider genetic risk evaluation?
Women and men of Ashkenazi Jewish ancestry at highest risk for carrying a BRCA mutation include those with:
- Breast cancer at age 65 or younger
- Triple negative breast cancer at any age
- Ovarian or fallopian tube cancer at any age
- More than one breast cancer diagnosis
- Male breast cancer
- Pancreatic cancer
- Metastatic prostate cancer
- A relative with a known mutation in a cancer risk gene
- A breast, ovarian, pancreatic, or high grade prostate cancer diagnosis in more than one individuals on the same side of the family
There has been an increasing discussion about BRCA testing in all individuals of Ashkenazi Jewish descent.
How do I collect my family history before my visit to a genetics professional?
Collect a detailed family history of cancer from blood-relatives on both your mother’s and father’s side of the family. This includes your first degree (parents, siblings, children), second degree (half-siblings, grandparents, aunts, uncles) and third degree (cousins, great grandparents, great-aunts, great-uncles) relatives. It is important to know the types of cancer your relatives have had and the ages when they were diagnosed. It is important to know the types of cancer your relatives have had and the ages when they were diagnosed.
How common are BRCA1 and BRCA2 mutations?
Individuals of Ashkenazi Jewish descent have a 1 in 40 chance of having a BRCA1 or BRCA2 mutation. This is about a five times greater probability than that of the general population.
Can women and men have BRCA mutations?
Both women and men can have BRCA mutations and pass them on to their male and female children.
What is the chance of passing on or inheriting a BRCA mutation?
If a mother or father has a mutation, there is a 50% chance of passing it on to each child. This means that some relatives may inherit the BRCA mutation in the family and some may not.
How much is BRCA testing and does insurance cover it?
The cost of BRCA genetic testing varies by the type of test done. Testing for the 3 most common BRCA mutations found in the Ashkenazi Jewish community costs several hundred dollars. These costs are often covered, either in part or in full, by insurance carriers when an individual meets certain testing criteria. Medicare typically covers genetic testing for individuals with a personal history of cancer. Medicaid coverage varies by state.
What if I do not have insurance or cannot afford my BRCA testing?
Some medical centers and testing labs have financial assistance programs to assist uninsured and underinsured individuals with the cost of their genetic testing.
Will a BRCA test result interfere with getting health insurance?
The Genetic Information Nondiscrimination Act (GINA) currently prevents employers and health insurance companies from discriminating against individuals based on their genetic information.
Are mutations in BRCA1 and BRCA2 the only ones that impact cancer risk?
Although mutations in the BRCA genes are important predictors of cancer risk, they are not the only gene mutations that can increase risk. A thorough risk assessment by a cancer genetics professional can help to determine if testing for other gene mutations is recommended.