Performance evaluation of the Elecsys PIVKA-II and Elecsys AFP assays for hepatocellular carcinoma diagnosis

被引:20
|
作者
Chan, Henry L. Y. [1 ]
Vogel, Arndt [2 ]
Berg, Thomas [3 ]
De Toni, Enrico N. [4 ]
Kudo, Masatoshi [12 ]
Trojan, Joerg [5 ]
Eiblmaier, Anja [6 ]
Klein, Hanns-Georg [7 ]
Hegel, Johannes Kolja [8 ]
Sharma, Ashish [13 ]
Madin, Kairat [9 ]
Rolny, Vinzent [10 ]
Lisy, Marcus-Rene [11 ]
Piratvisuth, Teerha [14 ]
机构
[1] Chinese Univ Hong Kong, Fac Med, Hong Kong, Peoples R China
[2] Hannover Med Sch, Clin Gastroenterol Hepatol & Endocrinol, Hannover, Germany
[3] Univ Leipzig, Dept Med 2, Div Hepatol, Med Ctr, Leipzig, Germany
[4] Ludwig Maximilian Univ Munich, Univ Hosp, Dept Med 2, Munich, Germany
[5] Goethe Univ Frankfurt, Dept Gastrointestinal Oncol, Frankfurt, Germany
[6] Microcoat Biotechnol GmbH, Lab Serv, Bernried, Germany
[7] MVZ Martinsried GmbH, Mol Oncol Dept, Planegg, Germany
[8] Lab Berlin Charite Vivantes Serv GmbH, Studies Collaborat & Innovat Management, Berlin, Germany
[9] Roche Diagnost GmbH, Global Study Management, Penzberg, Germany
[10] Roche Diagnost GmbH, New Technol Stat, Penzberg, Germany
[11] Roche Diagnost GmbH, Res & Dev, Penzberg, Germany
[12] Kindai Univ, Dept Gastroenterol & Hepatol, Fac Med, Osaka, Japan
[13] Roche Diagnost Int Ltd, Global Med & Sci Affairs, Rotkreuz, Switzerland
[14] Prince Songkla Univ, Fac Med, Hat Yai, Thailand
来源
JGH OPEN | 2022年 / 6卷 / 05期
关键词
acarboxyprothrombin; alpha-fetoprotein; diagnosis; hepatocellular carcinoma; prothrombin induced by vitamin K absence-II; ALPHA-FETOPROTEIN; PREDICTION; RISK;
D O I
10.1002/jgh3.12720
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Prothrombin induced by vitamin K absence-II (PIVKA-II) is a serum biomarker linked to hepatocellular carcinoma (HCC), showing superiority to alpha-fetoprotein (AFP) for early disease detection. We aimed to assess the clinical and analytical performance of the Elecsys (R) PIVKA-II immunoassay in diagnosing HCC and evaluate PIVKA-II's technical performance. Methods: Serum samples from adult cases (i.e. patients with a first-time HCC diagnosis; n = 168) and disease controls (i.e. patients without HCC with an at-risk condition; n = 208) were assessed. An AFP cut-off of 20 ng/mL was used to differentiate between HCC cases and disease controls. Clinical performance of the Elecsys PIVKA-II assay was compared with that of comparator assays (Lumipulse G PIVKA-II, mu TASWako DCP, ARCHITECT PIVKA-II) using receiver operating characteristic curve analysis to determine the area under the curve (AUC) values. Results: The Elecsys PIVKA-II assay compared favorably with comparator assays. Using a 28.4 ng/mL cut-off, the Elecsys PIVKA-II assay detected HCC with 86.9% sensitivity and 83.7% specificity. Clinical performance of the Elecsys PIVKA-II assay (AUC: 90.8%) was equivalent to that of comparator assays (AUC: 88.3-89.6%). Relatively high PIVKA-II concentrations were observed for cholangiocarcinoma and pancreatic cancer with the Elecsys assay in specificity panel analyses, indicating that high PIVKA-II concentrations should not be used alone in the absence of other clinical data. Conclusions: The Elecsys PIVKA-II assay showed good analytical performance under routine laboratory conditions, comparing favorably with comparator assays. These findings support the suitability of the Elecsys PIVKA-II assay as an aid in HCC diagnosis.
引用
收藏
页码:292 / 300
页数:9
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