Akademik Veri Yönetim Sistemi
Journal of Clinical Laboratory Analysis, cilt.25, sa.5, ss.350-353, 2011 (SCI-Expanded, Scopus)
α-Feto protein (AFP) is the widely used tumor marker in the diagnosis of hepatocellular carcinoma (HCC). The aim of this study was to assess the diagnostic and prognostic validity of a novel marker, serum Glypican-3 (GPC3) and to compare AFP in patients with HCC. One hundred and twenty-eight patients (75 patients with HCC, 55 patients with cirrhosis, and 28 healthy controls) were included in this study. Cut-off value of GPC3 was 3.9pg/ml. AFP was divided into four subgroups, according to cut-off values with 13, 20, 100, and 200ng/ml. Sensitivity, specificity, and positive and negative predictive values of GPC3 and AFP 13, AFP 20, AFP 100, AFP 200 subgroups and also GPC3+AFP 13, GPC3+AFP 20, GPC3+AFP 100, GPC3+AFP 200 combinations were compared. Serum GPC3 levels were significantly higher in patients with HCC and cirrhosis compared with control subjects (P<0.05). The median serum GPC3 levels were 3.9pg/ml in controls, 5.51pg/ml in patients with cirrhosis, and 5.13pg/ml in those with HCC. The median serum AFP levels were 1.37ng/ml in controls, 2.32ng/ml in cirrhotics, and 50.65ng/ml in HCC patients. The sensitivity, specificity, and positive and negative predictive values of GPC3 was 61.33, 41.82, 58.97, and 44.43%, respectively. The values for AFP were 68.57, 94.55, 94.12, and 70.27%, respectively. There was no correlation between GPC3 levels and prognostic parameters. GPC3 is not a useful diagnostic and prognostic marker for HCC. © 2011 Wiley-Liss, Inc.