[Development of clevudine resistance after switching from lamivudine in a patient with chronic hepatitis B]

Korean J Gastroenterol. 2008 Nov;52(5):325-8.
[Article in Korean]

Abstract

Clevudine is a nucleoside analog of the unnatural beta-L configuration which has potent antiviral activity against hepatitis B virus (HBV). Clevudine is expected to have similar pattern of resistance profile as lamivudine. However, there was no report on the mutation associated with clevudine resistance in patients with chronic hepatitis B. We report a case of young male patient with chronic hepatitis B who presented with clevudine resistance. The patient had received lamivudine therapy for 5 months with reduced serum HBV DNA levels. Then, lamivudine was switched to clevudine monotherapy. After the 6 months of clevudine therapy, the patient developed virologic breakthrough (>1.0chi10(8) copies/mL) as well as biochemical breakthrough, which was associated with the presence of rtM204I plus rtL80I mutant. After switching from clevudine to adefovir, the viral load decreased with biochemical improvement.

Publication types

  • Case Reports

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / therapeutic use
  • Adult
  • Amino Acid Substitution
  • Antiviral Agents / therapeutic use*
  • Arabinofuranosyluracil / analogs & derivatives*
  • Arabinofuranosyluracil / therapeutic use
  • Base Sequence
  • DNA, Viral / blood
  • Drug Resistance, Multiple, Viral
  • Hepatitis B e Antigens / metabolism
  • Hepatitis B, Chronic / drug therapy*
  • Hepatitis B, Chronic / genetics
  • Humans
  • Lamivudine / therapeutic use*
  • Male
  • Organophosphonates / therapeutic use
  • Reverse Transcriptase Inhibitors / therapeutic use*

Substances

  • Antiviral Agents
  • DNA, Viral
  • Hepatitis B e Antigens
  • Organophosphonates
  • Reverse Transcriptase Inhibitors
  • Lamivudine
  • Arabinofuranosyluracil
  • adefovir
  • clevudine
  • Adenine