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  4. Efficacy of entecavir therapy for hepatitis B e-antigen positive chronic hepatitis B patients with prior exposure to interferon or nucleoside/nucleotide analogues
 
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Efficacy of entecavir therapy for hepatitis B e-antigen positive chronic hepatitis B patients with prior exposure to interferon or nucleoside/nucleotide analogues

Journal
Hepatology Research
Journal Volume
46
Journal Issue
7
Pages
642-649
Date Issued
2016
Author(s)
Tseng K.-C.
Tseng C.-W.
Hsieh T.-Y.
Peng C.-Y.
Lin C.-L.
TUNG-HUNG SU  
TAI-CHUNG TSENG  
Lin H.H.
Wang C.-C.
JIA-HORNG KAO  
DOI
10.1111/hepr.12600
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84975065522&doi=10.1111%2fhepr.12600&partnerID=40&md5=a1fdc97b3630cd879aeffaaec2b1d79e
https://scholars.lib.ntu.edu.tw/handle/123456789/581913
Abstract
Aim: The efficacy of entecavir (ETV) in treatment-experienced chronic hepatitis B (CHB) patients remains unclear. We evaluated the therapeutic responses and virological breakthrough following ETV treatment in hepatitis B e-antigen (HBeAg) positive CHB patients with prior exposure to interferon or nucleoside/nucleotide analog and treatment-naive patients. Methods: This was a retrospective, multicenter study of treatment (>1?year) with 0.5?mg ETV in 248 treatment-naive and 48 treatment-experienced HBeAg positive CHB patients (70.5% male; mean age, 40.5?years). The rates of undetectable hepatitis B virus (HBV) DNA, HBeAg loss and virological breakthrough were analyzed. Results: The median duration of ETV treatment was 27.3?months (range, 18.4–34.5). The rate of HBeAg loss was 41.9% (104/248) in treatment-naive and 45.8% (22/48) in treatment-experienced patients. The baseline serum HBV DNA and alanine aminotransferase levels were significant predictors for HBeAg loss (P = 0.01 and P = 0.04, respectively). There was no statistical difference between the groups in the rates of undetectable HBV DNA and HBeAg loss at any time point. Virological breakthrough occurred in 1.6% (4/248) of treatment-naive and 8.3% (4/48) of treatment-experienced patients. The four treatment-experienced patients with virological breakthrough had received prior lamivudine treatment. After excluding those treated with interferon, lamivudine-experienced patients had significantly greater virological breakthrough compared with treatment-naive patients (log–rank test, P = 0.034; univariate Cox regression, P = 0.047). Conclusion: ETV treatment efficacy, including virological response and HBeAg loss, was comparable between treatment-naive and treatment-experienced HBeAg positive CHB patients. Lamivudine-experienced patients had a higher risk of virological breakthrough than treatment-naive patients. ? 2015 The Japan Society of Hepatology
Subjects
entecavir; hepatitis B virus; lamivudine
SDGs

[SDGs]SDG3

Other Subjects
alanine aminotransferase; entecavir; hepatitis B(e) antigen; interferon; lamivudine; nucleoside analog; virus DNA; adult; antigen detection; Article; chronic hepatitis B; controlled study; drug efficacy; drug exposure; female; follow up; human; liver cirrhosis; major clinical study; male; prediction; priority journal; retrospective study; treatment duration; treatment outcome; virus detection
Publisher
Blackwell Publishing Ltd
Type
journal article

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