Experience of Risk-reducing Salpingo-oophorectomy for a BRCA1 Mutation Carrier and Establishment of a System Performing a Preventive Surgery for Hereditary Breast and Ovarian Cancer Syndrome in Japan: Our Challenges for the Future

被引:12
作者
Hirasawa, Akira [1 ,2 ]
Masuda, Kenta [1 ]
Akahane, Tomoko [1 ]
Tsuruta, Tomohiko [1 ]
Banno, Kouji [1 ]
Makita, Kazuya [1 ]
Susumu, Nobuyuki [1 ]
Jinno, Hiromitsu [3 ]
Kitagawa, Yuko [3 ]
Sugano, Kokichi [2 ,3 ,4 ]
Kosaki, Kenjiro [2 ]
Aoki, Daisuke [1 ]
机构
[1] Keio Univ, Sch Med, Dept Obstet & Gynecol, Tokyo 1608582, Japan
[2] Keio Univ, Sch Med, Ctr Med Genet, Tokyo 1608582, Japan
[3] Keio Univ, Sch Med, Dept Surg, Tokyo 1608582, Japan
[4] Tochigi Canc Ctr, Res Inst, Canc Prevent Unit, Oncogene Res Unit, Mibu, Tochigi, Japan
关键词
hereditary breast and ovarian cancer syndrome; risk-reducing salpingo-oophorectomy; BRCA1; BRCA2; mutation carrier; ORAL-CONTRACEPTIVE USE; PROPHYLACTIC OOPHORECTOMY; SUSCEPTIBILITY GENE; WOMEN;
D O I
10.1093/jjco/hyt036
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Risk-reducing salpingo-oophorectomy is currently regarded as the most certain primary method for preventing ovarian cancer among BRCA1/2 mutation carriers with hereditary breast and ovarian cancer syndrome. However, risk-reducing salpingo-oophorectomy has rarely been performed in Japan. We developed the first system in Japan for performing risk-reducing salpingo-oophorectomy for BRCA1/2 mutation carriers at our university hospital in 2008. The indication for risk-reducing salpingo-oophorectomy for patients with hereditary breast/ovarian cancer syndrome is currently limited in Japan. This situation may be because of the limited number of genetic counseling units, the limited number of facilities that can perform BRCA1/2 genetic testing and the fact that prophylactic surgery is not covered by health insurance in Japan. Recent treatment guidelines for breast cancer in Japan recommended risk-reducing salpingo-oophorectomy for BRCA1/2 mutation carriers. Risk-reducing salpingo-oophorectomy should be performed in the framework of the standard therapeutic modality for BRCA1/2 mutation carriers in the near future.
引用
收藏
页码:515 / 519
页数:5
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