Chan Henry L Y, Vogel Arndt, Berg Thomas, De Toni Enrico N, Kudo Masatoshi, Trojan Jörg, Eiblmaier Anja, Klein Hanns-Georg, Hegel Johannes Kolja, Sharma Ashish, Madin Kairat, Rolny Vinzent, Lisy Marcus-Rene, Piratvisuth Teerha
Faculty of Medicine The Chinese University of Hong Kong Hong Kong China.
Clinic for Gastroenterology, Hepatology and Endocrinology Medizinische Hochschule Hannover Hannover Germany.
JGH Open. 2022 May 7;6(5):292-300. doi: 10.1002/jgh3.12720. eCollection 2022 May.
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® PIVKA-II immunoassay in diagnosing HCC and evaluate PIVKA-II's technical performance.
Serum samples from adult cases (i.e. patients with a first-time HCC diagnosis; = 168) and disease controls (i.e. patients without HCC with an at-risk condition; = 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, TASWako DCP, ARCHITECT PIVKA-II) using receiver operating characteristic curve analysis to determine the area under the curve (AUC) values.
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.
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.
维生素K缺乏诱导蛋白II(PIVKA-II)是一种与肝细胞癌(HCC)相关的血清生物标志物,在疾病早期检测方面显示出优于甲胎蛋白(AFP)的优势。我们旨在评估Elecsys® PIVKA-II免疫测定法在诊断HCC中的临床和分析性能,并评估PIVKA-II的技术性能。
对成年病例(即首次诊断为HCC的患者;n = 168)和疾病对照(即有风险状况但无HCC的患者;n = 208)的血清样本进行评估。使用20 ng/mL的AFP临界值来区分HCC病例和疾病对照。使用受试者工作特征曲线分析比较Elecsys PIVKA-II测定法与对照测定法(Lumipulse G PIVKA-II、TASWako DCP、ARCHITECT PIVKA-II)的临床性能,以确定曲线下面积(AUC)值。
Elecsys PIVKA-II测定法与对照测定法相比具有优势。使用28.4 ng/mL的临界值,Elecsys PIVKA-II测定法检测HCC的灵敏度为86.9%,特异性为83.7%。Elecsys PIVKA-II测定法的临床性能(AUC:90.8%)与对照测定法(AUC:88.3 - 89.6%)相当。在特异性分析中,Elecsys测定法检测到胆管癌和胰腺癌的PIVKA-II浓度相对较高,这表明在缺乏其他临床数据的情况下,不应单独使用高PIVKA-II浓度进行诊断。
Elecsys PIVKA-II测定法在常规实验室条件下显示出良好的分析性能,与对照测定法相比具有优势。这些结果支持Elecsys PIVKA-II测定法适用于辅助HCC诊断。