論文

査読有り
2012年

Clinical aspects of familial ovarian cancer - Current status and issues in Japan

Japanese Journal of Cancer and Chemotherapy
  • Masayuki Sekine
  • ,
  • Kosuke Yoshihara
  • ,
  • Kenichi Tanaka

39
4
開始ページ
506
終了ページ
511
記述言語
日本語
掲載種別
出版者・発行元
Japanese Journal of Cancer and Chemotherapy Publishers Inc.

Familial ovarian cancer occurs as part of two genetically distinct syndromes: hereditary breast and ovarian cancer (HBOC) and hereditary nonpolyposis colorectal cancer (HNPCC). HBOC caused by inherited mutations of BRCA1/2 and HNPCC caused by mismatch-repair genes are considered responsible for about 65 to 75% and 10 to 15% of familial ovarian cancers, respectively. Germline mutations of BRCA1 are considered responsible for about 50% of ovarian cancer families and 80% of breast-ovarian cancer families. BRCA2 mutations are less common than BRCA1 mutations in ovarian cancer families. A high proportion of serous adenocarcinomas at an advanced stage has been reported with BRCA-related ovarian cancers in several studies. It is controversial whether BRCA-related ovarian cancer patients carry a better prognosis despite the aggressive tu-mor-pathological characteristics of their disease, compared to sporadic cases. However, a good therapeutic response may be attributable to platinum-based chemotherapy. Recently in Japan, gene testing of BRCA1/2 has been available as a routine clinical test for diagnosing ovarian cancer families. Because the mutation spectrum of BRCA1/2 in Japanese was different from that of non-Ashkenazi individuals, the clinical application of BRCA1/2 gene testing for Japanese has been advocated. Approximately 1-5% of ovarian cancer patients in Japan are thought to have a family history of breast and/or ovarian cancer. The prevalence of deleterious mutations of BRCA1/2 in Japanese was reportedly significantly higher than that of non-Ashkenazi individuals despite the low frequency of familial cases in Japan. Although the age at diagnosis of ovarian cancers with BRCA1/2 mutation in the United States was earlier than those of the sporadic cases, there were no differences among Japanese. These results suggest that clinical and genetic aspects of BRCA-related ovarian cancer of the Japanese are different from those of Caucasians. A serious issue in this field is how the results will lead to a basis for the clinical application of a cancer prevention strategy targeting BRCA mutation carriers in Japanese.

リンク情報
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/22504673
URL
http://europepmc.org/abstract/med/22504673
URL
http://orcid.org/0000-0002-2254-3378
ID情報
  • ISSN : 0385-0684
  • ORCIDのPut Code : 9955768
  • PubMed ID : 22504673
  • SCOPUS ID : 84862583791

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