Volume 31, Issue 5 pp. 676-684

Efficacy and safety of prolonged 3-year telbivudine treatment in patients with chronic hepatitis B

Edward J. Gane

Edward J. Gane

New Zealand Liver Unit, Auckland City Hospital, Auckland, New Zealand

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Yuming Wang

Yuming Wang

Department of Infectious Diseases, Southwest Hospital, Third Military Medical University, Chongqing, China

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Yun-Fan Liaw

Yun-Fan Liaw

Liver Research Unit, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taipei, Taiwan

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JinLin Hou

JinLin Hou

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Satawat Thongsawat

Satawat Thongsawat

Department of Internal Medicine, Chiang Mai University, Chiang Mai, Thailand

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MoBin Wan

MoBin Wan

Department of Infectious Diseases, Shanghai Changhai Hospital, Shanghai, China

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Young M. Moon

Young M. Moon

Department of Internal Medicine, Kwan Dong University College of Medicine, Goyang, Korea

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JiDong Jia

JiDong Jia

Department of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, Beijing, China

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You C. Chao

You C. Chao

Division of Gastroenterology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan

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Junqi Niu

Junqi Niu

Department of Liver Diseases, First Hospital, University of Jilin, Changchun, China

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Nancy Leung

Nancy Leung

Department of Medicine, Alice Ho Miu Ling Nethersole Hospital, Hong Kong, China

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Didier Samuel

Didier Samuel

AP-HP Hôpital Paul Brousse, Centre Hépato-Biliaire, Villejuif, France

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Chao Wei Hsu

Chao Wei Hsu

Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taipei, Taiwan

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Weibin Bao

Weibin Bao

Novartis Pharmaceuticals, East Hanover, NJ, USA

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Patricia Lopez

Patricia Lopez

Novartis AG, Basel, Switzerland

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Claudio Avila

Claudio Avila

Novartis AG, Basel, Switzerland

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First published: 16 March 2011
Citations: 39
Correspondence
Edward J. Gane, MB, ChB, MD, FRACP, New Zealand Liver Transplant Unit, Auckland City Hospital, Private Bag 92024, Auckland 01142, New Zealand
Tel: +649 529 4001
Fax: +649 529 4061
e-mail: [email protected]

Abstract

Background: In the GLOBE trial, telbivudine demonstrated superior efficacy to lamivudine at 2 years in patients with chronic hepatitis B (CHB).

Aims: To investigate the long-term efficacy and safety of telbivudine in the telbivudine-treated cohort from the GLOBE trial.

Methods: Virological and biochemical responses were assessed in 213 HBeAg-positive and 186 HBeAg-negative CHB patients who continued telbivudine treatment for 3 years.

Results: Undetectable hepatitis B virus DNA and HBeAg seroconversions were achieved by 77 and 37% of HBeAg-positive patients respectively. Cumulative HBeAg seroconversion rate was 46%. HBeAg seroconversion was sustained at 52 weeks off therapy in 84% of the patients enrolled in the off-treatment follow-up arm of the study. Undetectable viraemia and normal alanine aminotransferase (ALT) levels at 3 years were achieved by 85 and 83% of HBeAg-negative patients respectively. Genotypic resistance rates for the study population who continued therapy during the third year were 11.3 in HBeAg-positive and 6.5% in HBeAg-negative patients. Patients with undetectable viraemia at treatment week 24 had optimal outcomes at 3 years. In the HBeAg-positive population, cumulative HBeAg seroconversion occurred in 58%. Resistance rates for HBeAg-positive and HBeAg-negative patients were 3.6 and 6.2% respectively. The telbivudine safety profile during prolonged therapy was similar to that in the GLOBE trial.

Conclusions: Three years of telbivudine treatment yielded high rates of viral suppression and ALT normalization with a favourable safety profile. High rates of HBeAg seroconversion were achieved with prolonged telbivudine therapy and were sustained in the majority of patients over 52 weeks off therapy.

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