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Long-term treatment outcomes of clevudine in antiviral-naive patients with chronic hepatitis B

Authors
Kim, Suk BaeSong, Il HanKim, Young MinNoh, RanKang, Ha YanLee, Hyang IeYang, Hyeon YoongKim, An NaChae, Hee BokLee, Sae HwanKim, Hong SooLee, Tae HeeKang, Young WooLee, Eaum SeokKim, Seok HyunLee, Byung SeokLee, Heon Young
Issue Date
21-Dec-2012
Publisher
Baishideng Publishing Group
Keywords
Chronic hepatitis B; Hepatitis B virus; Clevudine; Entecavir; Treatment outcomes
Citation
World Journal of Gastroenterology, v.18, no.47, pp 6943 - 6950
Pages
8
Journal Title
World Journal of Gastroenterology
Volume
18
Number
47
Start Page
6943
End Page
6950
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/14590
DOI
10.3748/wjg.v18.i47.6943
ISSN
1007-9327
2219-2840
Abstract
AIM: To evaluate the treatment outcomes of clevudine compared with entecavir in antiviral-naive patients with chronic hepatitis B (CHB). METHODS: We retrospectively analyzed the clinical data of CHB patients treated with clevudine 30 mg/d and compared their clinical outcomes with patients treated with entecavir 0.5 mg/d. The biochemical response, as assessed by serum alanine aminotransferase (ALT) activity, virologic response, as assessed by serum hepatitis B virus DNA (HBV DNA) titer, serologic response, as assessed by hepatitis B e antigen (HBeAg) status, and virologic breakthrough with genotypic mutations were assessed. RESULTS: Two-hundred and fifty-four patients [clevudine (n = 118) vs entecavir (n = 136)] were enrolled. In clevudine-treated patients, the cumulative rates of serum ALT normalization were 83.9% at week 48 and 91.5% at week 96 (80.9% and 91.2% in the entecavir group, respectively), the mean titer changes in serum HBV DNA were -6.03 and -6.55 log(10) copies/mL (-6.35 and -6.86 log(10) copies/mL, respectively, in the entecavir group), and the cumulative non-detection rates of serum HBV DNA were 72.6% and 83.1% (74.4% and 83.8%, respectively, in the entecavir group). These results were similar to those of entecavir-treated patients. The cumulative rates of HBeAg seroconversion were 21.8% at week 48 and 25.0% at week 96 in patients treated with clevudine, which was similar to patients treated with entecavir (22.8% and 27.7%, respectively). The virologic breakthrough in the clevudine group occurred in 9 (7.6%) patients at weeks 48 and 15 (12.7%) patients at week 96, which primarily corresponded to genotypic mutations of rtM204I and/or rtL180M. There was no virologic breakthrough in the entecavir group. CONCLUSION: In antiviral-naive CHB patients, long-term treatment outcomes of clevudine were not inferior to those of entecavir, except for virologic breakthrough. (C) 2012 Baishideng. All rights reserved.
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