Low-grade serous ovarian cancer: A review

被引:110
|
作者
Kaldawy, Anis [1 ,2 ]
Segev, Yakir [1 ,2 ]
Lavie, Ofer [1 ,2 ]
Auslender, Ron [1 ,2 ]
Sopik, Victoria [3 ]
Narod, Steven A. [3 ]
机构
[1] Carmel Hosp, Dept Obstet & Gynecol, Haifa, Israel
[2] Technion, Ruth & Bruce Rappaport Fac Med, Haifa, Israel
[3] Womens Coll Res Inst, Familial Breast Canc Res Unit, Toronto, ON, Canada
关键词
Epithelial ovarian cancer; Low-grade serous ovarian cancer; High-grade serous ovarian cancer; MAPK inhibitors; BRAF mutations; CLINICAL BEHAVIOR; BRAF MUTATION; BORDERLINE TUMORS; FOLLOW-UP; LOW-STAGE; CARCINOMA; WOMEN; SURVIVAL; FEATURES; THERAPY;
D O I
10.1016/j.ygyno.2016.08.320
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epithelial ovarian cancers can be divided into the more common, aggressive type II cancers and the less common, slow-growing type I cancers. Under this model, serous ovarian carcinomas can be subdivided into high-grade (type II) and low-grade (type I) tumours. The two-tier system for grading serous ovarian carcinomas is superior to more detailed grading systems in terms of predicting survival. Low-grade serous carcinomas typically present in young women and have a relatively good prognosis, despite being resistant to chemotherapy. Low-grade serous cancers have a high prevalence of KRAS and BRAF mutations, but a low prevalence of TP53 mutations (which are characteristic of high-grade serous cancers). Among women with low-grade serous ovarian cancer, the presence of a KRAS/BRAF mutation is a favorable prognostic factor. Studies of the mitogen-activated protein kinase (MAPK) inhibitor in low-grade serous ovarian cancer suggest that identifying MAPK mutations might eventually be useful in guiding treatment. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:433 / 438
页数:6
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