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Reappraisal of serum alpha‐foetoprotein as a surveillance test for hepatocellular carcinoma during entecavir treatment

Authors
Kim, Gi-AeSeock, Chang HyeonPark, Jang WonAn, Ji hyunLee, Kwang-SunYang, Jee EunLim, Young-SukKim, Kang MoShim, Ju HyunLee, DanbiLee, Han Chu
Issue Date
Jan-2015
Publisher
WILEY-BLACKWELL
Keywords
alpha-foetoprotein; entecavir; hepatocellular carcinoma
Citation
LIVER INTERNATIONAL, v.35, no.1, pp.232 - 239
Indexed
SCIE
SCOPUS
Journal Title
LIVER INTERNATIONAL
Volume
35
Number
1
Start Page
232
End Page
239
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/158051
DOI
10.1111/liv.12516
ISSN
1478-3223
Abstract
Background & Aims: The aim of this study was to re-evaluate the diagnostic performance of alpha-foetoprotein (AFP) as a surveillance test for hepatocellular carcinoma (HCC) in patients with hepatitis B virus-related chronic liver disease who were treated with entecavir (ETV). Methods: Between January 2007 and August 2012, we analysed 373 treatment-naïve patients with HBV-related chronic hepatitis (n = 229) or cirrhosis (n = 144) who were candidates for surveillance test, and were treated with ETV (0.5 mg/day) for longer than 12 months. To minimize the effect of AFP elevation caused by hepatitis activity, serum AFP levels were measured 12 months after the initiation of ETV treatment. Results: Hepatocellular carcinoma developed in 28 patients (7.5%) during a median follow-up period of 48.0 months (IQR = 40.5-57.3 months). The area under the receiver operating characteristic curve for AFP was 0.71 (95% CI = 0.59-0.84). The optimal AFP cut-off value was 13 ng/ml, leading to a sensitivity of 50.0%, specificity of 98.8%, positive predictive value of 77.8% and negative predictive value of 96.1%. In multivariate Cox analysis, an older age, the presence of cirrhosis and AFP levels of ≥20 ng/ml at 12 months after treatment were found to be significantly associated with an increased incidence of HCC. Conclusions: The role of serum AFP as a surveillance test should be re-evaluated in patients with HBV-related chronic liver diseases who were treated with antiviral therapy.
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