Literature DB >> 19065670

Early hepatitis B virus DNA reduction in hepatitis B e antigen-positive patients with chronic hepatitis B: A randomized international study of entecavir versus adefovir.

Nancy Leung1, Cheng-Yuan Peng, Hie-Won Hann, Jose Sollano, Judy Lao-Tan, Chao-Wei Hsu, Laurentius Lesmana, Man-Fung Yuen, Lennox Jeffers, Morris Sherman, Albert Min, Kimberly Mencarini, Ulysses Diva, Anne Cross, Richard Wilber, Juan Lopez-Talavera.   

Abstract

UNLABELLED: This study was undertaken to compare the early antiviral activity and viral kinetic profiles of entecavir (ETV) versus adefovir (ADV) in hepatitis B e antigen positive nucleoside-naïve adults with chronic hepatitis B (CHB). Sixty-nine nucleoside-naïve CHB patients with baseline HBV DNA of 10(8) copies/mL or more were randomized 1:1 to open-label treatment with entecavir 0.5 mg/day or adefovir 10 mg/day for a minimum of 52 weeks. The primary efficacy analysis compared mean reduction in HBV DNA at week 12 adjusted for baseline levels using linear regression. Entecavir was superior to adefovir for mean change from baseline in HBV DNA at week 12 (-6.23 log(10) copies/mL versus -4.42 log(10) copies/mL, respectively; mean difference -1.58 log(10) copies/mL; P < 0.0001). Both drugs demonstrated biphasic viral kinetics, with a first phase of rapid decline lasting 10 days. A significant difference favoring ETV was reached at day 10 (day 10 ETV-ADV difference estimate: -0.66 log(10) copies/mL; 95% CI [-0.30, -0.01]). Early virological response was found to be predictive of subsequent virological response, with those having lower HBV DNA levels at day 10 being more likely to achieve HBV DNA of less than 300 copies/mL at week 48. In addition, there was considerably less variability in the extent of HBV DNA reductions in patients treated with entecavir versus adefovir. Both the mean decrease in serum HBV DNA and the proportion of patients achieving HBV DNA less than 300 copies/mL were greater in entecavir-treated than adefovir-treated patients at weeks 2, 4, 8, 12, 24, and 48. At week 48, one (3%) ETV-treated versus 15 (47%) ADV-treated patients had HBV DNA of 10(5) copies/mL or more. Both antivirals were well tolerated.
CONCLUSION: Entecavir therapy resulted in earlier and superior reduction in HBV DNA compared with adefovir in nucleoside-naïve HBeAg-positive patients with CHB.

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Year:  2009        PMID: 19065670     DOI: 10.1002/hep.22658

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  42 in total

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Review 2.  Entecavir: a review of its use in chronic hepatitis B.

Authors:  Lesley J Scott; Gillian M Keating
Journal:  Drugs       Date:  2009-05-29       Impact factor: 9.546

3.  On-treatment monitoring of HBV DNA levels: predicting response and resistance to oral antiviral therapy at week 24 versus week 48.

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4.  The saga of entecavir.

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5.  Management of entecavir-resistant chronic hepatitis B with adefovir-based combination therapies.

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Journal:  World J Gastroenterol       Date:  2015-10-14       Impact factor: 5.742

Review 6.  Then and now: the progress in hepatitis B treatment over the past 20 years.

Authors:  Dina Halegoua-De Marzio; Hie-Won Hann
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Review 7.  Comparison of the 48-week efficacy between entecavir and adefovir in HBeAg-positive nucleos(t)ide-naïve Asian patients with chronic hepatitis B: a meta-analysis.

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8.  Predictors for efficacy of combination therapy with a nucleos(t)ide analogue and interferon for chronic hepatitis B.

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Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2017-08-08

9.  A Systematic Review of Side Effects of Nucleoside and Nucleotide Drugs Used for Treatment of Chronic Hepatitis B.

Authors:  Vandana Khungar; Steven-Huy Han
Journal:  Curr Hepat Rep       Date:  2010-04-21

10.  Th1 and Th2 immune response in chronic hepatitis B patients during a long-term treatment with adefovir dipivoxil.

Authors:  Yanfang Jiang; Zhenhua Ma; Guijie Xin; Hongqing Yan; Wanyu Li; Huining Xu; Chunhai Hao; Junqi Niu; Pingwei Zhao
Journal:  Mediators Inflamm       Date:  2010-11-29       Impact factor: 4.711

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