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用于肝细胞癌诊断的Elecsys PIVKA-II和Elecsys AFP检测的性能评估。

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

作者信息

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

机构信息

Faculty of Medicine The Chinese University of Hong Kong Hong Kong China.

Clinic for Gastroenterology, Hepatology and Endocrinology Medizinische Hochschule Hannover Hannover Germany.

出版信息

JGH Open. 2022 May 7;6(5):292-300. doi: 10.1002/jgh3.12720. eCollection 2022 May.

Abstract

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® 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;  = 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.

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.

摘要

背景与目的

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca66/9120909/647b59b2b3b1/JGH3-6-292-g002.jpg

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