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http://dx.doi.org/10.3904/kjim.2010.25.4.372

Efficacy of Initial Treatment with Clevudine in Naive Patients with Chronic Hepatitis B  

Yang, Hyeon-Woong (Department of Internal Medicine, Eulji University School of Medicine)
Lee, Byung-Seok (Department of Internal Medicine, Chungnam National University School of Medicine)
Lee, Tae-Hee (Department of Internal Medicine, Konyang University College of Medicine)
Lee, Heon-Young (Department of Internal Medicine, Chungnam National University School of Medicine)
Nam, Kwan-Woo (Department of Internal Medicine, Chungnam National University School of Medicine)
Kang, Young-Woo (Department of Internal Medicine, Konyang University College of Medicine)
Chae, Hee-Bok (Department of Internal Medicine, Chungbuk National University College of Medicine)
Kim, Seok-Hyun (Department of Internal Medicine, Chungnam National University School of Medicine)
Kim, Seok-Bae (Department of Internal Medicine, Dankook University College of Medicine)
Lee, Hyang-Ie (Department of Internal Medicine, Eulji University School of Medicine)
Kim, An-Na (Department of Internal Medicine, Eulji University School of Medicine)
Song, Il-Han (Department of Internal Medicine, Dankook University College of Medicine)
Lee, Sae-Hwan (Department of Internal Medicine, Soonchunhyang University College of Medicine)
Kim, Hong-Su (Department of Internal Medicine, Soonchunhyang University College of Medicine)
Publication Information
The Korean journal of internal medicine / v.25, no.4, 2010 , pp. 372-376 More about this Journal
Abstract
Background/Aims: Clevudine, a pyrimidine nucleoside analogue, has potent antiviral effects in patients with chronic viral hepatitis B (CHB). We report the efficacy of initial treatment with clevudine in naive patients with CHB living in Daejeon and Chungcheong Province, South Korea. Methods: One hundred five adults with CHB were administered 30 mg of clevudine per day for an average of 51 weeks. We evaluated viral markers and liver biochemistry retrospectively every 3 months. Results: Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and hepatitis B virus (HBV) DNA before the treatment were $184{\pm}188$ IU/L, $150{\pm}138$ IU/L, and $7.1{\pm}1.2$ log copies/mL, respectively. Undetectable rates (< 60 IU/mL) of DNA were 36.2%, 68.9%, 83.6%, 76.2%, and 75.8% at 12, 24, 36, 48, and 60 weeks, respectively. Seroconversion rates were 9.1%, 13.6%, 24.6%, 26.5%, and 26.1% and ALT normalization rates were 64.5%, 78.1%, 87.9%, 90.0% at 12, 24, 36, and 48 weeks, respectively. Six patients (5.7%) had a viral breakthrough. Conclusions: Clevudine is a useful drug in the initial treatment of patients with CHB, with a potent antiviral effect and low incidence of viral breakthrough.
Keywords
Clevudine; Drug resistance; HBV seroconversion; Hepatitis B; chronic;
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1 Yoo BC, Kim JH, Chung YH, et al. Twenty-four-week clevudine therapy showed potent and sustained antiviral activity in HBeAg-positive chronic hepatitis B. Hepatology 2007;45:1172-1178.   DOI   ScienceOn
2 Lim SG, Leung N, Hann HW, et al. Clinical trial: a phase II, randomized study evaluating the safety, pharmacokinetics and anti-viral activity of clevudine for 12 weeks in patients with chronic hepatitis B. Aliment Pharmacol Ther 2008;27:1282-1292.   DOI   ScienceOn
3 Niu C, Murakami E, Furman PA. Clevudine is efficiently phosphorylated to the active triphosphate form in primary human hepatocytes. Antivir Ther 2008;13:263-269.
4 Kim MH, Kim KA, Lee JS, et al. Efficacy of 48-week clevudine therapy for chronic hepatitis B. Korean J Hepatol 2009;15:331-337.   DOI   ScienceOn
5 Fischer KP, Gutfreund KS, Tyrrell DL. Lamivudine resistance in hepatitis B: mechanisms and clinical implications. Drug Resist Updat 2001;4:118-128.   DOI   ScienceOn
6 Ferenci P. Treatment of chronic viral hepatitis. Best Pract Res Clin Gastroenterol 2004;18 Suppl:113-120.   DOI   ScienceOn
7 Locarnini S. Molecular virology and the development of resistant mutants: implications for therapy. Semin Liver Dis 2005;25 Suppl 1:9-19.   DOI
8 Lok AS, Lai CL, Leung N, et al. Long-term safety of lamivudine treatment in patients with chronic hepatitis B. Gastroenterology 2003;125:1714-1722.   DOI   ScienceOn
9 Matthews SJ. Entecavir for the treatment of chronic hepatitis B virus infection. Clin Ther 2006;28:184-203.   DOI   ScienceOn
10 Koh KH, Kang CJ, Kim DH, et al. Development of clevudine resistance after switching from lamivudine in a patient with chronic hepatitis B. Korean J Gastroenterol 2008;52:325-328.
11 Liu SH, Grove KL, Cheng YC. Unique metabolism of a novel antiviral L-nucleoside analog, 2'-fluoro-5-methyl-beta-L-arabinofuranosyluracil: a substrate for both thymidine kinase and deoxycytidine kinase. Antimicrob Agents Chemother 1998;42:833-839.
12 Marcellin P, Mommeja-Marin H, Sacks SL, et al. A phase II doseescalating trial of clevudine in patients with chronic hepatitis B. Hepatology 2004;40:140-148.
13 Lee HS, Chung YH, Lee K, et al. A 12-week clevudine therapy showed potent and durable antiviral activity in HBeAg-positive chronic hepatitis B. Hepatology 2006;43:982-988.   DOI   ScienceOn
14 Yoo BC, Kim JH, Kim TH, et al. Clevudine is highly efficacious in hepatitis B e antigen-negative chronic hepatitis B with durable off-therapy viral suppression. Hepatology 2007;46:1041-1048.   DOI   ScienceOn
15 Lee KS, Byun KS, Chung YH, et al. Clevudine therapy for 24 weeks further reduced serum hepatitis B virus DNA levels and increased ALT normalization rates without emergence of viral breakthrough than 12 weeks of clevudine therapy. Intervirology 2007;50:296-302.   DOI   ScienceOn