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Physicians fail to recommend genetic testing to many high-risk breast cancer patients

Stanford School of Medicine News Feb 25, 2017

Physicians often fail to recommend genetic testing to breast cancer patients at high risk for cancer–associated mutations. Improving access to genetic counseling about the testing process and results is a key priority. Asian–Americans and older women were particularly likely to be “undertested.” Not testing these women represents a critical missed health care opportunity, the researchers said.

“We found that genetic counseling and testing are not well–matched to medical need,” said Allison Kurian, MD, associate professor of medicine and of health research and policy at Stanford. “Women are very interested in genetic testing but many fail to receive it. This is particularly worrisome because it means that doctors are missing the opportunity to prevent cancers in mutation carriers and their family members.”

Kurian is the lead author of the study, published online Feb. 7 in JAMA journal. University of Michigan researchers Reshma Jagsi, MD, DPhil, and Steven Katz, MD, MPH, share senior authorship.

Genetic testing can identify the presence of mutations in the BRCA1 and BRCA2 genes, which are strongly linked to the development of breast and ovarian cancers, as well as the presence of other cancer–related mutations.

Kurian and her colleagues surveyed 2,529 women with stage–0 to stage–2 breast cancer two months after surgery. The women were asked whether they wanted genetic testing and, if so, whether they had received it.

Although about two–thirds of the women said they wanted to be tested, only about one–third said they had been tested. About eight in 10 of those at highest risk for BRCA mutations wanted testing, but just over half of them were actually tested. About 56 percent of the women who were not tested attributed the lack of testing to the fact that it was not recommended by their physicians.

The survey also found that genetic counseling, either to help the patients decide whether to seek testing or to help them understand the results of their tests, often did not occur. Only about 40 percent of all high–risk women, and 60 percent of those high–risk women who were tested, reported having a genetic counseling session.
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