The Importance Of Genetic Testing For Ovarian Cancer
- Genetic testing provides valuable information that can help guide treatment for your specific type of cancer.
- A class of drugs called PARP inhibitors are now available for all women, though they benefit women with BRCA gene mutations the most
- Test results offer important information for family members who may not know they are carrying a particular gene mutation.
A large number of ovarian cancers, at least 10 to 15 percent that we know of, but probably more, are based on germline, or inherited, mutations, says Dr. Irina Dimitrova, gynecologic oncologist at Henry Ford Health System in Detroit. While lifestyle and chance play into a cancer diagnoses, inherited risk which is evaluated during genetic testing can play a huge role. Mutations of the BRCA gene, like BRCA-1 or BRCA-2, place women at a heightened risk for both ovarian and breast cancer.
Read MoreMen can also inherit a BRCA-1 or BRCA-2 mutation and an increased risk for certain cancers. Men with BRCA mutations have a higher than average lifetime risk for developing breast and prostate cancer. Their children have a 50 percent chance of carrying the same gene mutation, and the associated cancer risk.
Genetic testing after an ovarian cancer diagnosis can help your oncologist determine whether certain treatments may be right for your specific cancerespecially the promising family of PARP inhibitors, which work by preventing cancer cells from repairing their own DNA after chemotherapy. PARP inhibitors have been found to extend life for women at all stages of cancer treatment. Studies have shown they’re particularly effective in women with the BRCA gene. The PARP inhibitors olaparib (known by its brand name, Lynparza) and niraparib (brand name Zejula) are now approved to treat advanced ovarian cancer in the first-line setting, meaning before an initial round of chemotherapy.
The Food and Drug Administration has approved niraparib (brand name ZEJULA) for almost all women regardless of whether they have the BRCA mutation, as part of an initial course of treatment, or what’s called front-line treatment.
Most recently, the American Society of Clinical Oncology (ASCO) released new guidelines recommending PARP inhibitors be offered to women, with or without genetic mutations, who are newly diagnosed with stage III or IV ovarian cancer and have improved with chemotherapy.
If you're considering genetic testing, ask your relatives if they know of any family members who’ve had breast or ovarian cancer. A family history can indicate hereditary BRCA mutations, though someone can still carry a BRCA mutation without a family history of cancer.
Knowing your family medical history is an important part of taking charge of your health. It's important to keep this information up to date, and share it with your primary care doctor or other healthcare professionals regularly.
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