PIVKA-II在肝胆胰疾病中心筛查恶性肿瘤中的作用:一项大规模的现实世界研究

Chenghao Ge , Mingjie Luo , Kaiyuan Guo , Dong Zhu , Ning Han , Tengjiao Wang , Xiuying Zhao
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引用次数: 0

摘要

背景和目的维生素K缺失或拮抗剂II诱导的蛋白(PIVKA-II)是一种公认的诊断肝细胞癌(HCC)的生物标志物。尽管有报道称PIVKA-II的非特异性增加,但实际证据仍然很少。基于真实世界的数据,本研究旨在全面描述PIVKA-II在肝胆胰疾病中心的使用情况,并评估其在HCC或其他肝胆胰恶性肿瘤的初始筛查中的效用。方法本研究基于16215例患者的PIVKA-II结果和其他相关实验室检测(甲胎蛋白[AFP]、碳水化合物抗原19-9 [CA19-9]、肝功能、凝血指标、乙型肝炎病毒、丙型肝炎病毒)。然而,仅纳入了7809名符合条件个体的第一次PIVKA-II结果。进行组间比较、相关性分析和受试者工作特征曲线分析。结果spivka - ii检测结果在HCC(55.9%)、胆道癌(BC, 13.4%)、胃肠道和胰腺癌(6.3%)、良性疾病(23.5%)及健康人(0.92%)中均异常。PIVKA-II检测恶性肿瘤的曲线下面积为0.7754(0.7620-0.7688),检测HCC的曲线下面积为0.7509(0.7357-0.7662)。分层PIVKA-II值或将PIVKA-II与AFP或CA19-9联合使用有助于提高PIVKA-II对HCC的诊断效能。PIVKA-II值与HCC患者的AST和BC患者的胆红素显著正相关。结论:本研究确定了PIVKA-II在肝胆胰疾病中心恶性肿瘤筛查中的作用。我们还注意到,PIVKA-II联合AFP或对其价值进行分层后,PIVKA-II对HCC的诊断效果有所提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of PIVKA-II in screening for malignancies at a hepatobiliary and pancreatic disease center: A large-scale real-world study

Background and aims

Protein induced by vitamin K absence or antagonist II (PIVKA-II) is a well-accepted biomarker for diagnosing hepatocellular carcinoma (HCC). Although nonspecific increase of PIVKA-II has been reported, real-world evidence remains scarce. Based on real-world data, this study aimed to comprehensively describe the use of PIVKA-II at a hepatobiliary and pancreatic disease center and to assess its utility for the initial screening of HCC or other hepatobiliary–pancreatic malignancies.

Methods

This real-world retrospective study is based on the PIVKA-II results of 16,215 individuals and other relevant laboratory test (alpha-fetoprotein [AFP], carbohydrate antigen 19-9 [CA19-9], liver function, blood coagulation indicators, hepatitis B virus, and hepatitis C virus). However, only the first PIVKA-II results of 7809 eligible individuals were included. Between-group comparisons, correlation analysis, and receiver operating characteristic curve analysis were performed.

Results

PIVKA-II results were abnormal in patients with HCC (55.9%), biliary carcinoma (BC, 13.4%), gastrointestinal and pancreatic cancer (6.3%), and benign diseases (23.5%) as well as in healthy individuals (0.92%). The area under the curve of PIVKA-II for detecting malignancies was 0.7754 (0.7620–0.7688), whereas that for detecting HCC was 0.7509 (0.7357–0.7662). Stratifying the PIVKA-II values or combining PIVKA-II with AFP or CA19-9 helped improve the diagnostic performance of PIVKA-II for HCC. PIVKA-II values were significantly positively correlated with AST in patients with HCC and with bilirubin in patients with BC.

Conclusions

This study determined the role of PIVKA-II in malignancy screening at hepatobiliary and pancreatic disease centers. It was also noted that the diagnostic efficacy of PIVKA-II for HCC improved after combining PIVKA-II with AFP or stratifying its value.

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