Annals of Hepatology (May 2014)

Efficacy and safety of long term entecavir in chronic hepatitis B treatment naïve patients in clinical practice

  • Ezequiel Ridruejo,
  • Sebastián Marciano,
  • Omar Galdame,
  • María V. Reggiardo,
  • Alberto E. Muñoz,
  • Raúl Adrover,
  • Daniel Cocozzella,
  • Nora Fernandez,
  • Claudio Estepo,
  • Manuel Mendizabal,
  • Gustavo A. Romero,
  • Diana Levi,
  • Teresa Schroder,
  • Silvia Paz,
  • Hugo Fainboim,
  • Oscar G. Mandó,
  • Adrián C. Gadano,
  • Marcelo O. Silva

Journal volume & issue
Vol. 13, no. 3
pp. 327 – 336

Abstract

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Background and aims. Entecavir (ETV) is effective and safe in patients with chronic hepatitis B in the short term, but its long term efficacy and safety has not been established.Material and methods. We evaluated HBV DNA clearance, HBeAg/antiHBe and HBsAg/antiHBs seroconversion rates in HBeAg-positive and negative NUC naïve HBV patients treated with ETV for more than 6 months, and predictors of response.Results. A hundred and sixty nine consecutive patients were treated with ETV for a median of 181 weeks. 61% were HBeAg positive, 23% were cirrhotics, and mean HBV-DNA levels were 6,88 ± 1,74 log10 lU/mL. Overall, 156 (92%) patients became HBV DNA undetectable, 92 (88%) HBeAg positive and 64 (98%) HBeAg negative patients. Seventy four (71%) patients cleared HBeAg after a median of 48 weeks of treatment, 23 (14%) patients cleared HBsAg (19 HBeAg positive and 4 HBeAg negative, p 0.025) after a median of 96 weeks of treatment, and 22 (13%) patients developed protective titers of anti-HBs. At the end of the study, 35 (20%) patients had discontinued therapy: 33 HBeAg positive and 2 HBeAg negative; 9 of them (26%) developed virological relapse after a median of 48 weeks of stopping treatment. None of the patients had primary non response and one patient developed breakthrough. Two patients developed HCC, three underwent liver transplantation and 3 deaths were attributable to liver-related events. No serious adverse events were reported.Conclusion. Long term ETV treatment showed high virological response rates, and a favorable safety profile for NUC-naive HBeAg-positive and negative patients treated in clinical practice.

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