04:22am Sunday 17 December 2017

Screening for breast/ovarian cancer risk genes other than BRCA1/2 can change clinical recommendations

The report from a team led by a Massachusetts General Hospital (MGH) Cancer Center investigator is being published in the August issue of JAMA Oncology.

“The traditional approach has been to test most women with suspected hereditary risk for breast and/or ovarian cancer for BRCA1/2 alone,” explains senior author Leif Ellisen, MD, PhD, program director for Breast Medical Oncology at the MGH Cancer Center. “The concern about broader testing has been that the results really wouldn’t change what we told women about their risk and management – either because the risk associated with the other genes are not as high as for BRCA1/2 or because the clinical practice guidelines associated with other genes are less specific. Our study shows that, even under current practice guidelines, finding mutations in these other genes is likely to change the clinical management recommendations both for patients and for family members who also carry the associated mutations.”

The study examined whether use of currently available multigene panels to test for mutations in breast or ovarian cancer risk genes other than BRCA1/2 would change recommendations for women carrying those mutations. Investigators enrolled 1,069 patients who had been referred for genetic counseling for breast or ovarian cancer risk at MGH, Stanford University School of Medicine or Beth Israel Deaconess Medical Center and who did not carry BRCA1/2 mutations. For most participants, testing utilized one of two commercially available multigene panels – one a 25-gene panel, the other a 29-gene panel – screening genes associated with increased risk for breast and/or ovarian cancer and sometimes for other tumors.

Of all the screened patients, 63 were found to carry risk-associated mutations, most of which were consistent with their personal and family cancer histories. The 3.8 percent prevalence of these mutations among 1,046 patients tested with the two multigene panels – compared with 9 percent usually reported for BRCA1/2 mutations – is similar to what has been seen in previous studies. In almost one-third of these patients (20 of 63), the identified mutations were considered high-risk – including mutations associated with Lynch syndrome, which increases risk of colorectal, ovarian and other cancers. In each case, established guidelines for patients with those mutations would call for additional screenings and possibly preventive surgery that would not have been recommended on the basis of personal/family history alone.

Among those found to carry mutations conferring a low or moderate increase in cancer risk, current guidelines would have called for enhanced screening or preventive surgery for 10 patients with breast cancer risk genes and additional screening for 3 patients with mutations associated with pancreas cancer risk. Overall, 52 percent of patients in whom a mutation was identified would be recommended for additional screening or preventive measures above and beyond what would be called for by personal and family history. In addition, the presence of the identified mutations would lead to recommendations that close female relatives of 72 percent of the patients also be screened for the mutations, which if present would change their recommended clinical management as well.

“These results suggest that multi-gene testing can provide important additional information to guide recommendations for screening and prevention of future cancers,” Ellisen explains. “For example, results that point to a higher risk of breast cancer than would be predicted by history alone might call for breast MRI in addition to mammograms. The Lynch syndrome mutations signify a need for increased colorectal cancer screening and in some cases preventive hysterectomy or ovariectomy. But it’s important to note that multigene genetic testing is not appropriate for everyone and is most useful where personal and family histories suggest hereditary cancer, which is not the case for most patients with breast or ovarian cancer.”

A professor of Medicine at Harvard Medical School, Ellisen adds that the next step will be to examine whether recommendations based on multigene testing lead to better prevention, early detection and improved patient survival, a project that will take many years. “These future studies will help us refine and modify gene-based management recommendations over time. We’ve been testing for BRCA1/2 for more than 15 years, and outcome studies and guideline modifications are still ongoing. Genetic testing and its interpretation are getting more complex, so now more than ever, it makes sense for patients to seek out trained genetic counselors and practitioners to help them decide whether to be tested and how to interpret the test results.”

The lead author of the JAMA Oncology paper is Andrea Desmond of the MGH Cancer Center. Additional co-authors are Michele Gabree, MS, CGC, Nora Horick, MS, and Kristen Shannon, MS, CGC, MGH Cancer Center; Allison Kurian, MD, MSc, Meredith Mills, and James Ford, MD, Stanford University School of Medicine; Nadine Tung, MD, Beth Israel Deaconess Medical Center; and Michael Anderson, PhD, Yuya Kobayashi, PhD, Shan Yang, PhD, and Steven Lincoln, Invitae Corporation, which manufactures one of the multigene panels used in the study. The study was supported by grants from the MGH Friends Fighting Breast Cancer, the Tracey Davis Memorial Fund and the Breast Cancer Research Foundation.

Massachusetts General Hospital, founded in 1811, is the original and largest teaching hospital of Harvard Medical School. The MGH conducts the largest hospital-based research program in the United States, with an annual research budget of more than $760 million and major research centers in AIDS, cardiovascular research, cancer, computational and integrative biology, cutaneous biology, human genetics, medical imaging, neurodegenerative disorders, regenerative medicine, reproductive biology, systems biology, transplantation biology and photomedicine. In July 2015, MGH returned into the number one spot on the 2015-16 U.S. News & World Report list of “America’s Best Hospitals.”

Media Contacts: Katie Marquedant, kmarquedant@partners.org, 617 726-0337


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