Abstract

BackgroundThe purpose of this case-control study was to compare the prognoses of women with stage III mucinous ovarian carcinoma (MOC) who received maximal or optimal cytoreduction followed by paclitaxel plus carboplatin chemotherapy to those of women with stage III serous epithelial ovarian cancer (EOC) treated in the similar manner.MethodsWe performed a multicenter, retrospective review to identify patients with stage III MOC at seven gynecologic oncology departments in Turkey. Eighty-one women with MOC were included. Each case was matched to two women with stage III serous EOC in terms of age, tumor grade, substage of disease, and extent of residual disease. Survival estimates were measured using Kaplan-Meier plots. Variables predictive of outcome were analyzed using Cox regression models.ResultsWith a median follow-up of 54 months, the median progression-free survival (PFS) for women with stage III MOC was 18.0 months (95% CI; 13.8–22.1, SE: 2.13) compared to 29.0 months (95% CI; 24.04–33.95, SE: 2.52) in the serous group (p = 0.19). The 5-year overall survival rate of the MOC group was significantly lower than that of the serous EOC group (44.9% vs. 66.3%, respectively; p < 0.001). For the entire cohort, presence of multiple peritoneal implants (Hazard ratio [HR] 2.39; 95% confidence interval [CI], 1.38–4.14, p = 0.002) and mucinous histology (HR 2.28; 95% CI, 1.53–3.40, p < 0.001) were identified as independent predictors of decreased OS.ConclusionPatients with MOC seem to be 2.3 times more likely to die of their tumors when compared to women with serous EOC.

Highlights

  • Primary mucinous ovarian carcinoma (MOC) represents a biochemically and genetically distinct subgroup of epithelial ovarian cancer (EOC) [1]

  • Mucinous histology has consistently been reported as an independent adverse prognostic factor in advanced EOC [6, 8, 9] and the outcomes of MOCs are significantly different from EOCs with serous histology [10]

  • These 81cases were compared to 162 controls with serous EOC who had maximal or optimal CRS followed by paclitaxel plus carboplatin combination chemotherapy

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Summary

Introduction

Primary mucinous ovarian carcinoma (MOC) represents a biochemically and genetically distinct subgroup of epithelial ovarian cancer (EOC) [1]. The reason for poor prognosis of advanced MOC has been suggested to be either the aggressive biology of mucinous tumor or chemoresistance or both [9, 11, 12]. The purpose of this case-control study was to compare the prognoses of women with stage III mucinous ovarian carcinoma (MOC) who received maximal or optimal cytoreduction followed by paclitaxel plus carboplatin chemotherapy to those of women with stage III serous epithelial ovarian cancer (EOC) treated in the similar manner

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