Other cancers that have been associated with BRCA mutations are cervical, uterine, fallopian tube, colon, peritoneal, gallbladder, bile duct and melanoma cancers.
Several methods of screening may be used to look for BRCA mutations. When a family member has been identified as having a BRCA1 or BRCA2 mutation, tests can look for a specific harmful mutation in the genes that are affected. Multigene testing is used to look for harmful mutations in many genes.
Oncologists also look at their patient’s personal and family history to determine if they are at a greater likelihood of having a harmful BRCA mutation. These include:
When multiple family members have been diagnosed with the same cancer, testing for genetic mutations is recommended.
If willing to undergo testing, the first person that is still living, that has been diagnosed with the cancer will likely be the one that is tested to see if a genetic mutation exists. If that person tests positive for the genetic mutation, then insurance companies are more likely to cover the cost of additional testing for other family members who have the same cancer diagnosis or are at high risk.
Under the Affordable Care Act, insurance companies are required to pay for both genetic counseling and BRCA testing for women who meet the criteria outlined by the United States Preventive Services Task Force (USPSTF) guidelines. For individuals who qualify for this testing, insurance companies are required to cover the entire cost of genetic counseling and BRCA testing. Genetic counselors can help to determine if your genetic testing will be covered.
When recommended by a physician, most health insurance plans will cover the cost of genetic testing. Patients should verify with their insurance company to understand what type of services will be covered, prior to being tested.