Abstract

Aim. To determine whether the serum level of NGAL can discriminate cholangiocarcinoma from benign biliary tract disease in patients. Methods. This study was performed according to a prospective-specimen-collection, retrospective-blinded-evaluation (PRoBE) design. A total of 50 cholangiocarcinoma and 50 benign biliary tract disease cases were randomly selected from a cohort of consecutive cases of biliary tract diseases. Their sera were measured for the levels of NGAL and the widely used serum cholangiocarcinoma marker, carbohydrate antigen 19-9 (CA19-9). Results. The serum CA19-9 and NGAL levels were significantly elevated in cholangiocarcinoma patients (CA19-9: P < .001, NGAL: P < .001). The area under the curve (AUC) of a receiver operating characteristic (ROC) curve analysis for the diagnosis of cholangiocarcinoma of CA19-9 and NGAL was 0.81 and 0.79, respectively. Conclusion. The diagnostic accuracy of serum NGAL and CA19-9 makes them good candidates for use as biomarkers to discriminate cholangiocarcinoma patients from benign biliary tract disease patients.

Highlights

  • Cholangiocarcinoma (CCA) is one of the most aggressive malignant tumors and is associated with local invasiveness and a high rate of metastasis [1, 2]

  • The levels of serum bilirubin and alkaline phosphatase (ALP) were significantly higher in cholangiocarcinoma patients than in the control patients

  • There are two common tumor markers used for detecting cholangiocarcinoma, carcinoembryonic antigen (CEA), and carbohydrate antigen 19-9 (CA19-9) [16]

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Summary

Introduction

Cholangiocarcinoma (CCA) is one of the most aggressive malignant tumors and is associated with local invasiveness and a high rate of metastasis [1, 2]. Most cholangiocarcinoma patients present with symptoms of biliary tract obstruction. Many cases of benign biliary tract diseases present with similar clinical symptoms [3]. This tumor typically grows along the bile duct without projecting outward from the bile ducts as a forming mass. Computed tomography (CT), ultrasound, and magnetic resonance imaging (MRI) are often inadequate to reveal this lesion [4]. Identification of tumor markers in the serum would be beneficial in the clinical management of this disease

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