Gut and Liver · 2013 · 14 citations · 18 references
PharmacyInfectious DiseasesPharmacotherapyHepatitis PharmacotherapyMolecular VirologyVirologyAntiviral TherapyLiver DiseaseTreatment DurationViral HepatitisViral Hepatitis TreatmentChronic Viral HepatitisEntecavir TherapyGenotypic Resistance AssaysGenotypic Resistance ProfilingGenotypic Resistance TestingHbv Dna SuppressionHepatitis B TherapyHepatitis B Virus Resistance
BACKGROUND/AIMS: We investigated the efficacy of continuous long-term entecavir 0.5 mg treatment in naïve chronic hepatitis B patients showing a partial virologic response (PVR). METHODS: A total of 227 patients were included. PVR was defined as a more than 1 log10 IU/mL decline in detectable serum hepatitis B virus (HBV) DNA by polymerase chain reaction (PCR; ≥20 IU/mL) at week 48. A complete virologic response (CVR) was defined as undetectable serum HBV DNA by PCR (<20 IU/mL) at week 48. RESULTS: At week 48, the rate of the PVR was 64/227 (28.2%). Among patients with PVR, the cumulative rates of virologic response (serum HBV DNA <20 IU/mL) at weeks 96 and 144 were 45.2% and 73.8%, respectively. The cumulative rates of genotypic resistance were not significantly different between patients with a PVR and patients with a CVR (p=0.057). However, the cumulative rates of virologic breakthrough were higher in patients with PVR than in patients with CVR (4% vs 0% and 11.2% vs 0% at weeks 96 and 144, respectively; p<0.001). CONCLUSIONS: Long-term continuous entecavir 0.5 mg treatment in patients with a PVR resulted in an additional virologic response without a significant increase in genotypic resistance. However, the rate of virologic breakthrough was higher in the partial responders.
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EASL clinical practice guidelines management of chronic hepatitis B
张学武, Xu Li · Inter J Epidemiol Infect Dis · 2009 · 1.5K citations
EASL Clinical Practice Guidelines: Management of chronic hepatitis B
Journal of Hepatology · 2008 · 1.3K citations