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Adefovir and Lamivudine Combination Therapy in Patients with Entecavir-Resistant Chronic Hepatitis B: Antiviral Responses and Evolution of Mutations

Authors
Yim, Hyung JoonLee, Hyun JungSuh, Sang JunSeo, Yeon SeokKim, Chang WookLee, Chang DonPark, Sang HoonLee, Myung SeokPark, Choong KeeChae, Hee BokKim, Moon YoungBaik, Soon KooKim, Yun SooKim, Ju HyunIl Lee, JungHong, Sun PyoUm, Soon Ho
Issue Date
2014
Publisher
KARGER
Keywords
Adefovir; Chronic hepatitis B; Entecavir; Lamivudine; Resistance
Citation
INTERVIROLOGY, v.57, no.5, pp.239 - 247
Indexed
SCIE
SCOPUS
Journal Title
INTERVIROLOGY
Volume
57
Number
5
Start Page
239
End Page
247
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/101206
DOI
10.1159/000360399
ISSN
0300-5526
Abstract
Objective: This study was designed to prospectively evaluate the antiviral responses and evolution of resistance mutations during adefovir (ADV) plus lannivudine (LMV) therapy in patients with entecavir (ETV)-resistant hepatitis B virus (HBV) infection. Methods: Twenty chronic hepatitis B (CHB) patients who had been receiving ETV for more than 6 months and developed virologic breakthrough due to ETV resistance were consecutively enrolled. Results: Patients received ADV plus LMV therapy for 12 months. The baseline mean serum HBV DNA level was 5.59 +/- 1.28 log(10) IU/ml. The rtT184L/1/A/F (50%), rtS202G (25%) and mixed ETV-resistant mutations (25%) were detected at enrollment. The mean reduction in serum HBV DNA levels from baseline to 12 months was -2.3 +/- 1.06 log(10) IU/ml (p < 0.001). Seventeen patients were followed up for the full 12 months, and complete virologic response (HBV DNA <20 IU/ml) was observed in 4 patients (23.5%). Among the remaining 13 patients who still had detectable HBV DNA, 7 patients showed disappearance of ETV-resistant mutations or reduction of the proportion of ETV-resistant mutants. An ADV- and LMV-resistant mutant (rtA181T) emerged in 2 patients (11.7%). Conclusions: ADV plus LMV combination therapy suppresses ETV-resistant mutants in the viral population and significantly reduces serum HBV DNA levels in ETV-resistant CHB patients. (C) 2014 S. Karger AG, Basel
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