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Abstract

The World Health Organization (WHO) classifies ovarian neoplasms according to their histological differentiation, namely epithelial tumors, germ cell tumors, and sex cord-stromal cell tumors [1]. Epithelial ovarian tumor represents the largest group, accounting for 91 % of malignant cases. Serous carcinoma is the most common epithelial subtype [2]. Epithelial ovarian cancer (EOC) is now recognized as a heterogeneous disease and is divided according to histologic subtypes: high-grade serous, low-grade serous, endometrioid, clear cell, mucinous, and Brenner carcinoma. Each histologic subtype is associated with distinct histologic features, molecular genetics, and clinical behavior. The etiology of EOC remains unclear [3]. Several factors, including genetic, reproductive, hormonal, and behavioral factors have been suggested to increase the risk for ovarian cancer. Genetic factors have the strongest and most consistent association with increased risk of EOC. At least 10 % of all EOC are reported to be hereditary, with the majority (about 80 %) of these related to mutations in BRCA genes and 10 % related to mutations associated with the Lynch syndrome [4]. Currently, the standard treatment of ovarian cancer includes cytoreductive surgery and combination chemotherapy with a platinum-doublet. This approach yields a 5-year overall survival, all stages combined, of 44 % [2]. The main reason for poor outcome is the advanced stage at diagnosis. Patients diagnosed at early stages have a 75 % chance of cure. This article will not focus on the screening for ovarian cancer. For a discussion of ovarian cancer screening see Menon et al.[5].

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Rittiluechai, K., Ji, Y., Lounsbury, K., Howe, A., Verschraegen, C. (2015). Ovarian Cancer. In: de Mello, R., Tavares, Á., Mountzios, G. (eds) International Manual of Oncology Practice. Springer, Cham. https://doi.org/10.1007/978-3-319-21683-6_18

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