Abstract

To evaluate the diagnostic accuracy of cancer antigen 125 (CA125) and complete blood count (CBC) parameters, such as the neutrophil to lymphocyte ratio (NLR), the platelet to lymphocyte ratio (PLR), and thrombocytosis in patients with ovarian masses. The present is a retrospective study conducted at a single tertiary hospital from January 2010 to November 2016. We included consecutive women referred due to suspicious adnexal masses. The CBC and CA125 were measured in the serum of 528 women with ovarian masses before surgery or biopsy. We evaluated the diagnostic performance of the NLR, PLR, platelets (PLTs), CA125, and the associations between them. We tested the clinical utility of the CBC parameters and CA125 in the discrimination of ovarian masses through decision curve analysis (DCA). The best balance between sensitivity and specificity was obtained by the associations of CA125 or PLTs ≥ 350/nL, with 70.14% and 71.66%, CA125 or PLTs ≥ 400/nL, with 67.30% and 81.79%, CA125 or PLR, with 76.3% and 64.87%, and CA125 or NLR, with 71.09% and 73.89% respectively. In the DCA, no isolated CBC parameter presented a higher clinical utility than CA125 alone. We showed that no CBC parameter was superior to CA125 in the prediction of the malignancy of ovarian tumors in the preoperative scenario.

Highlights

  • Ovarian cancer (OC) is the second most lethal gynecological cancer worldwide, it is relatively rare.[1]

  • We showed that no complete blood count (CBC) parameter was superior to cancer antigen 125 (CA125) in the prediction of the malignancy of ovarian tumors in the preoperative scenario

  • Since chronic inflammation plays a fundamental role in the pathogenesis of OC,[2] several studies[3,4,5,6,7,8] have investigated systemic inflammatory response (SIR) markers obtained from a simple complete blood count (CBC), such as the neutrophil to lymphocyte ratio (NLR), the platelet to lymphocyte ratio (PLR), and the platelet (PLT) count

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Summary

Introduction

Ovarian cancer (OC) is the second most lethal gynecological cancer worldwide, it is relatively rare.[1]. Since chronic inflammation plays a fundamental role in the pathogenesis of OC,[2] several studies[3,4,5,6,7,8] have investigated systemic inflammatory response (SIR) markers obtained from a simple complete blood count (CBC), such as the neutrophil to lymphocyte ratio (NLR), the platelet to lymphocyte ratio (PLR), and the platelet (PLT) count They have been evaluated as relevant prognostic factors in OC,[3,4] but a few studies[5,6,7,8] have focused their usefulness in the prediction of malignancy in the preoperative setting

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