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Efficacy of telbivudine compared with entecavir in hepatitis B virus-related cirrhosis: 2 year follow-up data

Authors
Kim, Hae RimYim, Hyung JoonKang, SeongheeSuh, Sang JunKim, Seung YoungHyun, Jong JinKoo, Ja SeolKim, Ji HoonSeo, Yeon SeokYeon, Jong EunLee, Sang WooByun, Kwan SooUm, Soon Ho
Issue Date
3월-2015
Publisher
WILEY-BLACKWELL
Keywords
cirrhosis; entecavir; hepatitis B; telbivudine
Citation
LIVER INTERNATIONAL, v.35, no.3, pp.860 - 869
Indexed
SCIE
SCOPUS
Journal Title
LIVER INTERNATIONAL
Volume
35
Number
3
Start Page
860
End Page
869
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/94181
DOI
10.1111/liv.12605
ISSN
1478-3223
Abstract
Background & AimsEntecavir (ETV) is effective in the treatment of chronic hepatitis B virus (HBV) infections, even in patients with underlying cirrhosis. However, there is little information on the effect of telbivudine (TBV) in chronic hepatitis B patients with cirrhosis.This study compared the antiviral efficacy of TBV and ETV in HBV-related cirrhosis. MethodsWe consecutively enrolled 151 treatment-naive patients with HBV-related cirrhosis who started antiviral therapy with TBV (n=61) or ETV (n=90). ResultsAfter 24months of treatment, per-protocol analysis showed similar virological response rates (HBV DNA <20IU/ml) in the TBV group (80.6%, 25/31) and in the ETV group (90.2%, 74/82) (P=0.167). However, intention-to-treat analysis showed lower virological response rates in the TBV group (41.7%, 25/60) than in the ETV group (83.1%, 74/89) (P=0.001). Mean reduction in HBV DNA levels was greater in the ETV group (-3.721.94 vs. -4.87 +/- 1.57 respectively, P=0.001). Serologic and biochemical response rates at month 24 did not differ significantly between the groups. Child-Turcotte-Pugh score was significantly improved after 24months compared to the pretreatment state without difference between the groups. During 24months of therapy, 15 patients (27.3%) showed antiviral resistance to TBV while no resistance (0%) was reported in the ETV group (P=0.001). ConclusionsCompared to ETV, TBV therapy shows lower efficacy in viral suppression and higher risk of antiviral resistance despite comparable effect on improvement of hepatic function for the treatment of HBV-related cirrhosis.
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