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Managing ovarian cancer risk in women with BRCA1/2 genetic variants

08.12.19 | Canadian Medical Association Journal

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A new review to help physicians manage the risk of ovarian cancer in women who carry the BRCA1/2 gene mutations is published in CMAJ (Canadian Medical Association Journal) .

BRCA1 and BRCA2 genetic variants are a clinically important risk factor for the development of ovarian and breast cancer, and women who carry these variants have a lifetime risk of ovarian cancer of 39%-44% and 11%-17%, respectively.

"Given the substantial lifetime risk and high mortality of ovarian cancer in women with BRCA1/2 variants, risk reduction is a priority," says Dr. Melissa Walker, a fifth-year resident in obstetrics and gynecology at the University of Toronto, Toronto, Ontario.

The review, which looked at 46 articles published between 2014 and 2019, provides guidance on screening, preventive surgery, contraception and management of menopausal symptoms.

Highlights:

"Women with these variants have unique and broad medical needs that cross medical specialties and areas of expertise, from surgery to genetics, oncology to nursing, menopause specialists to social work." says Dr. Walker. "Multidisciplinary management of these women is essential."

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How to Cite This Article

APA:
Canadian Medical Association Journal. (2019, August 12). Managing ovarian cancer risk in women with BRCA1/2 genetic variants. Brightsurf News. https://www.brightsurf.com/news/LQMO0YX1/managing-ovarian-cancer-risk-in-women-with-brca12-genetic-variants.html
MLA:
"Managing ovarian cancer risk in women with BRCA1/2 genetic variants." Brightsurf News, Aug. 12 2019, https://www.brightsurf.com/news/LQMO0YX1/managing-ovarian-cancer-risk-in-women-with-brca12-genetic-variants.html.