Many women with breast cancer are concerned about the genetic risk of developing other cancers themselves or of a loved one developing cancer. These findings were published in the Journal of Clinical Oncology (2015; doi:10.1200/JCO.2014.58.5885).
Overall, 35% of women with breast cancer expressed a strong desire for genetic testing, but 43% of those women did not have a relevant discussion with a health care professional. The study also found that racial minority patients with a strong desire for testing were less likely than white patients to discuss it with a professional, even though studies show that minority patients are not at lower risk for these mutations.
“Our findings suggest a marked unmet need for discussion about genetic risk,” said study author Reshma Jagsi, MD, DPhil, associate professor of radiation oncology at the University of Michigan Medical School in Ann Arbor.
Approximately 5% to 10% of breast cancer patients have an inherited genetic mutation that drives their cancer. Many of the women who reported interest in genetic testing were at low risk of having a mutation and doctors would not typically discuss genetic risk with them.
“With recent judicial opinions, direct-to-consumer marketing, and celebrity reports, the public has become much more aware that genetic testing is available. But genetic risk is complex. Even patients unlikely to have elevated genetic risk may still benefit from a discussion,” Jagsi said.
The researchers surveyed 1,536 women who had been treated for breast cancer. Patients were identified through the Surveillance, Epidemiology and End Results databases from Detroit and Los Angeles.
Patients who had a strong desire for testing reported that they were worried other members of their family might get breast cancer in the future. Worry was highest among Latinas who spoke only Spanish, where 83% reported this concern.
In addition, these women were more likely to report worry about their own risks when evaluated in long-term follow-up as survivors. Nearly half of those who had an unmet need for discussion about genetic testing were worried about breast cancer. Only one-quarter of those who did not have unmet need reported this worry.
“By addressing genetic risk with patients, we can better inform them of their true risk of cancer returning or of developing a new cancer. This could potentially alleviate worry and reduce confusion about cancer risk,” said Jagsi.
Women who have a genetic mutation face a higher risk of developing a second breast cancer and may wish to consider more aggressive treatment, preventive measures, or additional screening.