Entecavir: a step forward in combating hepatitis B disease


Yurdaydin C.

EXPERT OPINION ON PHARMACOTHERAPY, vol.9, no.17, pp.3095-3109, 2008 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Review
  • Volume: 9 Issue: 17
  • Publication Date: 2008
  • Doi Number: 10.1517/14656560802515546
  • Journal Name: EXPERT OPINION ON PHARMACOTHERAPY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.3095-3109
  • Keywords: Entecavir, metabolism, pharmacodynamics, safety and efficacy, NUCLEOSIDE-NAIVE PATIENTS, ADEFOVIR DIPIVOXIL, HEPATOCELLULAR-CARCINOMA, NATURAL-HISTORY, VIRUS-DNA, PEGINTERFERON ALPHA-2A, WOODCHUCK MODEL, LAMIVUDINE, HBEAG, EFFICACY
  • Ankara University Affiliated: No

Abstract

Background: Entecavir (ETV) is a potent deoxyguanosine nucleoside analog with a very good safety record. Objectives/methods: This review provides a comprehensive overview on the mechanism of action, pharmacodynamics, pharmacokinetics, clinical efficacy and safety of entecavir obtained through an extensive literature search. Results/conclusion: ETV inhibits all three steps of hepatitis B virus replication via entecavir - triphosphate, its intracellular active form, by dose-dependently competing with deoxyguanosine triphosphate for incorporation into DNA. Superior efficacy of ETV over lamivudine (LVD) has been shown in four double-blind, randomized controlled clinical trials encompassing a large cohort of treatment naive HBeAg-positive and HBeAg-negative patients and LVD-refractory HBeAg-positive patients. Prolongation of ETV treatment is associated with further improvement of efficacy. In treatment-naive patients, cumulative probability of ETV resistance and viral breakthrough after 5 years of treatment has been reported as 1.2 and 0.8%, respectively. ETV displays low cytotoxicity in proliferating cultured liver cell and has an excellent safety in clinical use.