It is estimated that 5-10% of all breast cancers are inherited. Most inherited cases of breast cancer are associated with two genes called BRCA1 (BReast CAncer gene 1) and BRCA2 (breast cancer gene 2).
Women with a BRCA1 or BRCA2 gene mutation have a significantly increased risk for breast and ovarian cancer. In addition, BRCA mutations are associated with an increased risk for male breast cancer, as well as prostate, pancreatic and other cancers. Determining if an individual has a BRCA1 or BRCA2 gene mutation can dramatically impact screening and medical management recommendations and also allow other family members to be tested to better assess their risks.
Family History Risks for Breast Cancer
Individuals with a personal or family history which includes any of the following may be interested in cancer risk assessment and genetic counseling:
- Multiple family members with breast and/or ovarian cancer
- Pre-menopausal breast cancer
- Bilateral breast cancer
- Male breast cancer
- Eastern European (Ashkenazi) Jewish ancestry.
Our Cancer Genetics Screening Program provides genetic counseling and testing for people concerned about their personal and/or family history of cancer. The program offers an extensive review of personal and family health history, assessment of cancer risks and the likelihood of a BRCA mutation in the family, coordination and interpretation of genetic testing, personalized screening and management recommendations.
What You Need to Know
What is breast cancer gene testing?
It is estimated that 5 percent to 10 percent of all breast cancers are inherited. Most inherited cases of breast cancer are associated with two genes called BRCA1 (BReast CAncer gene 1) and BRCA2 (breast cancer gene 2). Genetic testing is a DNA blood (or saliva) test, which looks for changes (mutations) in the BRCA1 and BRCA2 genes that cause an increased risk for developing breast and ovarian cancer.
Should every woman have breast cancer gene testing?
No, at this time, breast cancer gene testing is offered to families that meet certain criteria. The prevalence of BRCA1 and BRCA2 gene mutations in the general population is about one in 500 people. Therefore, it is not common enough to screen the entire general population, and it would be cost prohibitive. Also, genetic testing isn’t perfect. There can sometimes be ambiguous or uncertain results. Certain characteristics of a family medical history may qualify a person for genetic testing.
- What are the red flags you look for in a family history, which might suggest a hereditary link?
What steps should I take to better understand my risk for breast cancer?
Obtaining a detailed medical family history is very important, as risk assessment is highly dependent on family history. Here is the type of information you should collect:
- Who in the family has had cancer (blood relatives)
- Type of cancer in the family (where the cancer started)
- Approximate age at which the cancer was first diagnosed
Talk with your doctor about your family history; a referral to a genetic counselor may be appropriate.
What is a genetic counselor?
Genetic counselors are advanced practice providers, specialty trained in interpreting family history and genetic testing. Through the process of genetic counseling, they help people gain a basic understanding of genetics and disease risk. In addition, they facilitate the genetic testing process and provide support for decision making.
Is genetic testing covered by most insurance companies?
Yes, it is usually covered by insurance when medically indicated. There has to be a reasonable likelihood that the gene is in the family, and we have to determine how the genetic testing will impact medical management. The genetic counselor will help to facilitate any required insurance pre-authorizations after the genetic counseling appointment.
If someone has a breast cancer gene mutation, what can be done about it?
The goal of genetic counseling and testing is for the prevention and early detection of cancer. Women who are found to have a breast cancer gene mutation meet with our team of specialists who have experience in managing patients at an increase risk for cancer. They will discuss medical management decisions which may include: additional surveillance (such as breast MRI), medications that can reduce the risk of cancer and surgical options.
This is just one example of how our specialists at are putting personalized medicine into practice. Personalized medicine is about understanding your risk factors for a disease, in this case cancer, and making personal decisions based on your own philosophies, your priorities in life, your family, and your lifestyle — to take control of your health, make informed decisions, and practice disease prevention and early detection.
Virtual Visits Are Available
Safe and convenient virtual visits by video let you get the care you need via a mobile device, tablet or computer wherever you are. We’ll gather your medical records for you and get our experts’ input so we can offer treatment options without an in-person visit. To schedule a virtual visit, call 1-866-680-0505.
Cancer and the COVID-19 Vaccine
There is currently no data that suggests current or former cancer patients should avoid getting the COVID-19 vaccine. Cancer can weaken your immune system, so we recommend that most patients get the vaccine as soon as possible.