Effectiveness of PIVKA-II in the detection of hepatocellular carcinoma based on real-world clinical data

被引:79
作者
Yu, Rentao [1 ,2 ]
Tan, Zhaoxia [1 ,2 ]
Xiang, Xiaomei [1 ,2 ]
Dan, Yunjie [1 ,2 ]
Deng, Guohong [1 ,2 ,3 ]
机构
[1] Third Mil Med Univ, Southwest Hosp, Dept Infect Dis, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Chongqing Key Lab Infect Dis, Southwest Hosp, Chongqing 400038, Peoples R China
[3] Third Mil Med Univ, Inst Immunol, Chongqing 400038, Peoples R China
基金
中国国家自然科学基金;
关键词
PIVKA-II; HCC; Real-world; AFP; Surveillance; GAMMA-CARBOXY PROTHROMBIN; CHRONIC HEPATITIS-B; VITAMIN-K ABSENCE; ALPHA-FETOPROTEIN; ENZYME-IMMUNOASSAY; INTERFERON-ALPHA; ANTAGONIST-II; RISK; EPIDEMIOLOGY; MANAGEMENT;
D O I
10.1186/s12885-017-3609-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Protein Induced by Vitamin K Absence or Antagonist-II (PIVKA-II) is an efficient biomarker specific for hepatocellular carcinoma (HCC). Some researchers have proved that levels of PIVKA-II reflect HCC oncogenesis and progression. However, the effectiveness of PIVKA-II based on real-world clnical data has barely been studied. Methods: A total of 14,861 samples were tested in Southwest Hospital in over 2 years' time. Among them, 4073 samples were PIVKA-II positive. Finally, a total of 2070 patients with at least two image examinations were enrolled in this study. Levels of AFP and PIVKA-II were measured by chemiluminescence enzyme immunoassay (CLEIA) and chemiluminescent microparticle Immunoassay (CMIA), respectively. Results: A total of 1016 patients with HCC were detected by PIVKA-II in a real-world application. In all these cases, 88.7% cases primarily occurred and patients with advanced HCC covered 61.3%. Levels of PIVKA-II were significantly higher in advanced group (4650.0 mAU/ml, 667.0-33,438.0 mAU/ml) than early-stage group (104.5 mAU/ml, 61.0-348.8 mAU/ml; P < 0.001). Levels of PIVKA-II elevated significantly in recurrence and residual group than recovery group (P < 0.001). A total of 1054 PIVKA-II positive patients were non-HCC cases. Among them, cirrhosis took the largest part (46.3%), followed by hepatitis (20.6%) and benign nodules (15.3%). High-levels of PIVKA-II in at-risk patients is an indicator of HCC development in two-year time. Conclusions: Our data showed that PIVKA-II effectively increases the detection rate of HCC was a valid complement to AFP and image examination in HCC surveillance.
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页数:10
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