| Literature DB >> 25279173 |
Kanako Nakamura1, Kouji Banno1, Megumi Yanokura1, Miho Iida1, Masataka Adachi1, Kenta Masuda1, Arisa Ueki1, Yusuke Kobayashi1, Hiroyuki Nomura1, Akira Hirasawa1, Eiichiro Tominaga1, Daisuke Aoki1.
Abstract
Lynch syndrome is a hereditary ovarian cancer with a prevalence of 0.9-2.7%. Lynch syndrome accounts for 10-15% of hereditary ovarian cancers, while hereditary breast and ovarian cancer syndrome accounts for 65-75% of these cancers. The lifetime risk for ovarian cancer in families with Lynch syndrome is ~8%, which is lower than colorectal and endometrial cancers, and ovarian cancer is not listed in the Amsterdam Criteria II. More than half of sporadic ovarian cancers are diagnosed in stage III or IV, but ≥80% of ovarian cancers in Lynch syndrome are diagnosed in stage I or II. Ovarian cancers in Lynch syndrome mostly have non-serous histology and different properties from those of sporadic ovarian cancers. A screening method for ovarian cancers in Lynch syndrome has yet to be established and clinical studies of prophylactic administration of oral contraceptives are not available. However, molecular profiles at the genetic level indicate that ovarian cancer in Lynch syndrome has a more favorable prognosis than sporadic ovarian cancer. Inhibitors of the phosphatidylinositol 3-kinase/mammalian target of the rapamycin pathway and anti-epidermal growth factor antibodies may have efficacy for the disease. To the best of our knowledge, this is the first review focusing on ovarian cancer in Lynch syndrome.Entities:
Keywords: chemoprevention; lynch syndrome; ovarian cancer; risk-reducing surgery; surveillance
Year: 2014 PMID: 25279173 PMCID: PMC4179837 DOI: 10.3892/mco.2014.397
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450