학술논문

Combination adefovir-lamivudine prevents emergence of adefovir resistance in lamivudine-resistant hepatitis B
Document Type
Report
Author abstract
Source
Journal of Gastroenterology and Hepatology. Sept, 2007, Vol. 22 Issue 9, p1500, 6 p.
Subject
Hepatitis B -- Prevention
Language
English
ISSN
0815-9319
Abstract
To purchase or authenticate to the full-text of this article, please visit this link: http://dx.doi.org/10.1111/j.1440-1746.2007.05093.x Byline: David van der Poorten (1,), Emilia Prakoso (1,[dagger]), Teh-Liane Khoo (*), Meng C Ngu (*), Geoffrey W McCaughan ([dagger]), Simone I Strasser ([dagger]), Alice U Lee (*) Keywords: adefovir; adefovir resistance; hepatitis B; lamivudine Abstract: Abstract Background and Aim: The outcomes of lamivudine-resistant chronic hepatitis B patients treated with long-term adefovir dipivoxil have not been well described. This study aims to characterize the virological and biochemical response and to determine factors that may influence the development of resistance to adefovir. Methods: A retrospective review was conducted on all patients with lamivudine-resistant chronic hepatitis B treated with adefovir for a minimum of 6 months at two tertiary referral centers. Results: Data on 161 patients were analyzed. Seventy-two percent achieved an initial virological response with eventual normalization of alanine aminotransferase in only 67% of patients. Seventeen patients developed adefovir resistance with cumulative resistance rates of 3.2%, 8.8%, and 18% at 12, 24, and 36 months, respectively. Twelve (71%) of these patients had a biochemical breakthrough, with one death from fulminant hepatic failure. The median duration of lamivudine crossover was 1 month in adefovir-resistant patients, compared with 12 months for the remainder of the cohort (P < 0.01). Longer crossover therapy reduced the adefovir resistance rate, but did not eliminate it. No adefovir resistance is reported in those who were continued on long-term combination lamivudine-adefovir without a period of adefovir monotherapy. Conclusions: Combination lamivudine-adefovir therapy protected against the emergence of adefovir resistance. Author Affiliation: (*)Department of Gastroenterology and Hepatology, Concord Hospital, and ([dagger])AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia Article History: Accepted for publication 16 May 2007. Article note: Dr Alice U Lee, Department of Gastroenterology and Hepatology, Concord Hospital, Sydney, NSW 2139, Australia. Email: leea@email.cs.nsw.gov.au