European Journal of Obstetrics & Gynecology and Reproductive Biology
Does synchronous endometrioid endometrial cancer have any prognostic effect on Stage I endometrioid ovarian cancer?
Introduction
Ovarian cancer is the most lethal of all the gynaecological cancers [1]. Recent data have shown that ovarian cancer has two distinct histological types, and each type has a completely different pathogenesis [2]. Type 1 tumours arise from ovarian surface epithelium and mullerian inclusions, either from endosalpingiosis or invagination of the ovarian surface epithelium during repair of ovulation or implantation of cells from the endometrium. This process typically involves a relatively slow and multistep pathway, and accounts for many early-stage cancers such as endometrioid, clear cell, mucinous, and low-grade serous cancers. In contrast, the more common high-grade serous cancers (Type 2) have a phenotype that resembles the fallopian tube mucosa, and they commonly have p53 mutations. These tumours appear to develop rapidly, and are almost always at an advanced stage at presentation.
Endometrioid ovarian cancer (EOC) is a Type 1 tumour that has specific clinical and pathological features. It usually presents as early-stage disease and well-differentiated histology. Another distinct property of EOC is its frequent co-occurrence with synchronous endometrial tumours [3]. Synchronous endometrial and ovarian cancer (SEOC) is seen in approximately 10% of all women with ovarian cancer and 5% of all women with endometrial cancer [4]. Women with SEOC differ from women with primary endometrial or ovarian cancer alone, particularly in terms of prognosis. The prognostic effect of synchronous endometrial endometrioid cancer (SEEC) in the management of EOC has been a subject of debate in the literature. Therefore, this study sought to determine the prognostic effect of SEEC on Stage 1 EOC.
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Materials and methods
After obtaining approval from the Institutional Review Board, the study population was identified by searching the gynaecologic oncology and pathology database. Thirty-one patients with Stage 1 EOC who underwent comprehensive surgical staging between January 2000 and November 2013 were included in the study. All patients underwent total abdominal hysterectomy, bilateral salpingo-oophorectomy, omentectomy, and bilateral pelvic and para-aortic lymph node dissection. The patients were divided into
Results
Fifteen women with FIGO Stage 1 EOC with SEEC were classed as Group 1 and 16 patients who had FIGO Stage 1 EOC alone were classed as Group 2. The mean age of all patients was 48.2 [standard deviation (SD) 8.6] years, the mean age of patients in Group 1 was 49 (SD 8.0), and the mean age of patients in Group 2 was 47.6 (SD 9.2) years. The two groups were similar in terms of age (p = 0.685). None of the patients had a family history of colon, gastric or breast cancer, and no secondary malignancies
Discussion
Approximately 1–2% of all women with gynaecological cancers have two or more simultaneous independent primary tumours involving the female genital tract. Some are coincidental tumours of completely different histological types, and each of them requires treatment on its own merit. However, synchronous tumours of similar or identical histology occur, and this is almost unique to the female genital tract [10]. It is important to distinguish between low-stage multiple primary tumours and tumours
Conflict of interest
None declared.
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