Original Article
Copyright ©2013 Baishideng Publishing Group Co.
World J Gastroenterol. Jan 21, 2013; 19(3): 339-346
Published online Jan 21, 2013. doi: 10.3748/wjg.v19.i3.339
Figure 1
Figure 1 α-fetoprotein (A), α-fetoprotein-L3 (B) and prothrombin induced by vitamin K absence-II (C) values in benign liver disease and hepatocellular carcinoma patients. α-fetoprotein (AFP)-L3 and prothrombin induced by vitamin K absence (PIVKA)-II levels are plotted by AFP concentrations (AFP < 20 ng/mL, AFP 20-200 ng/mL and AFP > 200 ng/mL). In patients with AFP < 20 ng/mL, AFP-L3 levels were higher in hepatocellular carcinoma (HCC) (P < 0.001) (B). In patients with AFP 20-200 ng/mL, PIVKA-II showed higher levels in HCC (P = 0.010) (C). The horizontal dotted lines are cut-off values used for performance analysis in this study. BLD: Benign liver disease.
Figure 2
Figure 2 Receiver operating characteristic curves of total α-fetoprotein, α-fetoprotein-L3, prothrombin induced by vitamin K absence-II and three combined markers for the diagnosis of hepatocellular carcinoma in all patients. The area under the curve values were 0.879 for total α-fetoprotein (AFP), 0.887 for AFP-L3, 0.801 for prothrombin induced by vitamin K absence (PIVKA)-II and 0.959 for the three combined markers.
Figure 3
Figure 3 Receiver operating characteristic curves of α-fetoprotein-L3 and prothrombin induced by vitamin K absence-II for the diagnosis of hepatocellular carcinoma in patients with total α-fetoprotein < 20 ng/mL. The area under the curve values were 0.824 for α-fetoprotein (AFP)-L3, 0.774 for prothrombin induced by vitamin K absence (PIVKA)-II and 0.939 for the two combined markers.