Protein induced by vitamin K absence or antagonist-Ⅱ versus alpha-fetoprotein in the diagnosis of hepatocellular carcinoma: A systematic review with meta-analysis

Verfasser / Beitragende:
Feng Shen; Tian Yang; Hao Xing; Zhen-Li Li; Yi-Jie Zheng; Jun Han; Wan-Yee Lau; Han Zhang
Ort, Verlag, Jahr:
Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Naval Medical University, Shanghai 200438, China%Medical Scientific Affairs, Abbott Diagnostics, Shanghai 200003, China%Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Naval Medical University, Shanghai 200438, China, 2018
Faculty of Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, China,
Zeitschriftentitel:
Hepatobiliary & pancreatic diseases international, Jg. 17; H. 6; S. 487 - 495
Format:
Journal Article
Online Zugang:
ID: FETCH-wanfang_journals_gjgdybzz_z2018060053

Background: As a promising biomarker of hepatocellular carcinoma (HCC), protein induced by vitamin K absence or antagonist-Ⅱ (PIVKA-II) has been studied extensively. However, its diagnostic capability varies across HCC studies. This study aimed to compare the performance of PIVKA-II with alpha-fetoprotein (AFP) in the diagnosis of HCC. Data sources: A systematic literature search was conducted to identify the studies from MEDLINE, Em-base and Cochrane Library Databases, which were published up to December 20, 2017 to compare the diagnostic capability of PIVKA-II and AFP for HCC. The data were pooled using random effects model. Pooled sensitivity and specificity were calculated. Summary receiver operating characteristic curve (ROC) was employed to evaluate the diagnostic accuracy of each marker. Results: Thirty-one studies were included. The pooled sensitivity (95% CI) of PIVKA-II and AFP was 0.66 (0.65–0.68) and 0.66 (0.65–0.67), respectively in diagnosis of HCC; and the corresponding pooled speci-ficity (95%

Hepatobiliary & pancreatic diseases international

Meta-analyses; Hepatocellular carcinoma; Protein induced by vitamin K absence or antagonist-; Alpha-fetoprotein