Gastroenterology
Volume 130, Issue 7 , Pages 2039-2049, June 2006

Entecavir for Treatment of Lamivudine-Refractory, HBeAg-Positive Chronic Hepatitis B

Data presented in part at the 55th Annual Meeting of the American Association for the Study of Liver Diseases 2004 (Abstract 1152), the 14th Biennial Meeting of the Asia Pacific Association for the Study of the Liver 2004 (Abstract 46), the Therapies for Viral Hepatitis Workshop 2004 (Abstract 42), the 1st Annual Winter Meeting of the Canadian Association for the Study of the Liver 2005 (Abstract 91), and the 13th World Congress of Gastroenterology 2005 (Abstract R.0780).

  • Morris Sherman

      Affiliations

    • Department of Medicine, Toronto General Hospital, Toronto, Ontario, Canada
    • Corresponding Author InformationAddress requests for reprints to: Morris Sherman, MD, Toronto General Hospital, 9N-981, 200 Elizabeth Street, Toronto, Ontario M5G2C4, Canada. fax: (416) 591-2107
  • ,
  • Cihan Yurdaydin

      Affiliations

    • Ankara University Medical School, Ankara, Turkey
  • ,
  • Jose Sollano

      Affiliations

    • University of Santo Tomas, Manila, Philippines
  • ,
  • Marcelo Silva

      Affiliations

    • Hospital Universitario Austral, Pilar, Argentina
  • ,
  • Yun–Fan Liaw

      Affiliations

    • Chang Gung Memorial Hospital and University, Taipei, Taiwan
  • ,
  • Janusz Cianciara

      Affiliations

    • Medical University of Warsaw, Warsaw, Poland
  • ,
  • Anna Boron–Kaczmarska

      Affiliations

    • Department of Infectious Diseases, Pomeranian Medical University, Szczecin, Poland
  • ,
  • Paul Martin

      Affiliations

    • Mount Sinai School of Medicine, New York, New York
  • ,
  • Zachary Goodman

      Affiliations

    • Armed Forces Institute of Pathology, Washington, DC, USA
  • ,
  • Richard Colonno

      Affiliations

    • Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey, and Wallingford, Connecticut
  • ,
  • Anne Cross

      Affiliations

    • Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey, and Wallingford, Connecticut
  • ,
  • Gail Denisky

      Affiliations

    • Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey, and Wallingford, Connecticut
  • ,
  • Bruce Kreter

      Affiliations

    • Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey, and Wallingford, Connecticut
  • ,
  • Robert Hindes

      Affiliations

    • Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey, and Wallingford, Connecticut
  • ,
  • AI463026 BEHoLD Study Group

Received 20 September 2005; accepted 9 March 2006.

Background & Aims: Lamivudine treatment is associated with frequent development of resistant hepatitis B virus (HBV) and loss of treatment benefit. In preclinical and phase II studies, entecavir demonstrated potent antiviral activity against lamivudine-resistant HBV. Methods: In this phase III, double-blind trial, hepatitis B e antigen-positive patients who were refractory to lamivudine therapy (persistent viremia or documented YMDD mutations while receiving lamivudine) were randomized to switch to entecavir 1 mg daily (n = 141) or continue lamivudine 100 mg daily (n = 145) for a minimum of 52 weeks. Two coprimary end points were assessed at 48 weeks: histologic improvement and a composite end point (HBV branched DNA <0.7 MEq/mL and alanine aminotransferase [ALT] <1.25 times the upper limit of normal). Results: Histologic improvement occurred in 55% (68/124) of entecavir-treated vs 28% (32/116) of lamivudine-treated patients (P < .0001). More patients on entecavir than lamivudine achieved the composite end point: 55% (77/141) vs 4% (6/145), respectively (P < .0001). Mean change from baseline in HBV DNA was −5.11 log10 copies/mL for entecavir-treated patients and −0.48 log10 copies/mL for lamivudine-treated patients (P < .0001). Virologic rebound because of entecavir resistance substitutions occurred in 2 of 141 of entecavir-treated patients, and genotypic evidence of resistance was detected in 10 patients. The safety profile of entecavir was comparable to lamivudine with fewer ALT flares on treatment. Conclusions: In patients with lamivudine-refractory chronic hepatitis B, switching to entecavir provides superior histologic improvement, viral load reduction, and ALT normalization compared with continuing lamivudine, with a comparable adverse event profile.

Abbreviations used in this paper: ALT, alanine aminotransferase, CHB, chronic hepatitis B, HBV, hepatitis B virus, ULN, upper limit of normal, INR, international normalized ratio

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PII: S0016-5085(06)00735-9

doi:10.1053/j.gastro.2006.04.007

Refers to article:

  • Continuing Medical Education Exams 2: June 2006

    Gastroenterology June 2006 (Vol. 130, Issue 7, Page 2207)

Gastroenterology
Volume 130, Issue 7 , Pages 2039-2049, June 2006