Forefront Magazine | Volume 7, Issue 4, 2018
Research team led by Mayo Clinic IDs genes that boost the risk of triple-negative breast cancer: Mayo Clinic Forefront cancer magazine.
A research team led by Fergus J. Couch, Ph.D., has identified specific genes associated with an increased risk of developing triple-negative breast cancer. Their research findings were published in the Journal of the National Cancer Institute in August 2018.
"Triple-negative breast cancer is an aggressive type of cancer that can't be treated using targeted therapies," said Dr. Couch, a geneticist at Mayo Clinic in Rochester, Minnesota. "It accounts for 15 percent of breast cancer in the Caucasian population and 35 percent in the African-American population. It is also associated with a high risk of recurrence and a poor five-year survival rate. Our findings provide the basis for better risk management."
Dr. Couch said germ line genetic testing, which evaluates inherited genetic changes that increase the risk of certain cancers in an individual, has helped identify women at increased risk of breast cancer. However, it has been more difficult to identify women at elevated risk of triple-negative breast cancer because only inherited mutations in BRCA1 have been linked to this subtype of breast cancer.
Dr. Couch and his colleagues performed genetic testing on 10,901 patients with triple-negative breast cancer from two studies. They tested 21 cancer predisposition genes in 8,753 patients and 17 genes in the other 2,148 patients. They found that alterations in BARD1, BRCA1, BRCA2, PALB2 and RAD51D genes were associated with a high risk of triple-negative breast cancer and a greater than 20 percent lifetime risk of overall breast cancer among Caucasians. They observed a similar trend among African-Americans. In addition, mutations in the BRIP1 and RAD51C genes were linked to a more moderate risk of triple-negative breast cancer.
"This study is the first to establish which genes are associated with high lifetime risks of triple-negative breast cancer," Dr. Couch said. "While previous studies have found genetic variants in patients with BARD1, BRIP1, PALB2 and RAD51C triple-negative breast cancer, the current study shows this in more detail, and identifies new specific and strong associations between the susceptibility genes RAD51D and BARD1, and triple-negative breast cancer risk."
The findings will enable expanded genetic testing to identify women at risk of triple-negative breast cancer and may potentially lead to better prevention strategies, he said. The findings may also lead to revisions to the screening guidelines of the National Comprehensive Cancer Network (NCCN), which currently recommend BRCA testing only when a patient has a family history of breast cancer or is diagnosed at age 60 or younger.Related