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By Amy Orciari Herman
Edited by André Sofair, MD, MPH
A review in the Canadian Medical Association Journal outlines steps clinicians can take in managing ovarian cancer risk in women with BRCA1/2 pathogenic variants.
Among the key points, based on an analysis of 46 articles:
Women with a known or likely family history of pathogenic BRCA1/2 mutations should undergo genetic testing under the guidance of a genetic counselor (a comprehensive list of BRCA1/2 testing indications is provided in the review).
No screening method for ovarian cancer has been shown to reduce mortality, even in high-risk women.
Salpingo-oophorectomy can reduce ovarian cancer risk by roughly 80%. It should be performed at ages 35 to 40 in women with a BRCA1 mutation and at ages 40 to 45 in those with a BRCA2 mutation.
Women who have salpingo-oophorectomy to lower their ovarian cancer risk should take hormone therapy (provided they don't have a history of breast cancer) until they reach the average age of menopause.
Comment
LINK(S):
CMAJ review (Free abstract)
Background: NEJM Journal Watch Women's Health coverage of U.S. guidelines on managing hereditary breast and ovarian cancer syndrome (Free)