Diagnostic value of serum PIVKA-II levels for BCLC early hepatocellular carcinoma and correlation with HBV DNA

被引:9
|
作者
Wu, Jiali [1 ]
Xiang, Zheyi [1 ]
Bai, Le [1 ]
He, Lagu [1 ]
Tan, Li [1 ]
Hu, Min [1 ]
Ren, Yaping [1 ]
机构
[1] Cent South Univ, Dept Lab Med, Xiangya Hosp 2, Changsha 410011, Hunan, Peoples R China
关键词
Hepatocellular carcinoma; prothrombin induced by vitamin K absence-II; alpha fetoprotein; HBV DNA load; vascular invasion; DES-GAMMA-CARBOXYPROTHROMBIN; CLINICAL-PRACTICE GUIDELINES; ALPHA-FETOPROTEIN; CARBOXY PROTHROMBIN; CHRONIC HEPATITIS; CANCER STATISTICS; MANAGEMENT; PREDICTORS; EXPRESSION; BIOMARKERS;
D O I
10.3233/CBM-181402
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: It is reported that prothrombin induced by vitamin K absence-II (PIVKA-II) has a better performance of diagnosis for HCC, and has also been known to be an independent risk factor for vascular invasion. Few studies study the relationship between PIVKA-II and HBV DNA. OBJECTIVE: To determine the clinical value of serum Prothrombin induced by vitamin K absence-II (PIVKA-II) in early hepatocellular carcinoma (HCC), and to explore its relationship with vascular invasion and HBV DNA. METHODS: In a Chinese cohort, we conducted a case-control study to compare the performances of a-fetoprotein (AFP) and PIVKA-II serum levels for diagnosis of HCC and early HCC. Fifty one healthy controls, 37 chronic hepatitis patients, 43 cirrhotic patients and 143 HCC cases of which 48 (33.57%) had early stage HCC (n = 19 very early, n = 29 early) were enrolled. We explored the correlation between PIVKA-II serum level and several pathological features such as vascular invasion. The serum levels of and AFP were measured by chemiluminescence assay (CLIA) and electrochemiluminescence assay (ECLA). RESULTS: The serum levels of both PIVKA-II and AFP in HCC group were higher than that in chronic hepatitis, cirrhosis and healthy control groups. The sensitivity, specificity, positive predictive value, negative predictive value and kappa of PIVKA-II were higher than AFP in the diagnosis of HCC. Serum PIVKA-II level was correlated with tumor size, tumor cell differentiation and BCLC staging (P < 0.05). For the diagnosis of early HCC, the combination of PIVKA-II (AUC 0.812; 95% CI, 0.7020.894) and AFP (0.797; 95% CI, 0.686-0.883) slightly improve the diagnostic performance for early HCC(AUC 0.849; 95% CI, 0.745-0.923). PIVKA-II > 166 mAU/ml is an independent risk factor for vascular invasion. The serum HBV DNA level in cirrhosis and HCC patients was significantly higher than in chronic hepatitis patients. We detected a negative association between serum PIVKA-II and serum HBV DNA levels. CONCLUSIONS: PIVKA-II was more efficient than AFP for the diagnosis of early HCC and has no correlation with serum HBV DNA levels.
引用
收藏
页码:235 / 242
页数:8
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