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Final analysis of the international observational S-Collate study of peginterferon alfa-2a in patients with chronic hepatitis B
P. Marcellin, Q. Xie, S. Woon Paik, R. Flisiak, T. Piratvisuth, J. Petersen, T. Asselah, M. Cornberg, D. Ouzan, GR. Foster, G. Papatheodoridis, D. Messinger, L. Regep, G. Bakalos, U. Alshuth, P. Lampertico, H. Wedemeyer,
Language English Country United States
Document type Journal Article, Multicenter Study, Observational Study, Research Support, Non-U.S. Gov't
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- MeSH
- Safety MeSH
- Hepatitis B, Chronic drug therapy metabolism MeSH
- Adult MeSH
- Hepatitis B e Antigens metabolism MeSH
- Hepatitis B Surface Antigens metabolism MeSH
- Interferon-alpha adverse effects therapeutic use MeSH
- Internationality * MeSH
- Humans MeSH
- Polyethylene Glycols adverse effects therapeutic use MeSH
- Recombinant Proteins adverse effects therapeutic use MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Observational Study MeSH
- Research Support, Non-U.S. Gov't MeSH
BACKGROUND AND AIMS: Sustained off-treatment immune control is achievable in a proportion of patients with chronic hepatitis B treated with peginterferon alfa-2a. We evaluated on-treatment predictors of hepatitis B surface antigen (HBsAg) clearance 3 years after peginterferon alfa-2a treatment and determined the incidence of hepatocellular carcinoma. METHODS: A prospective, international, multicenter, observational study in patients with chronic hepatitis B who have been prescribed peginterferon alfa-2a (40KD) in a real-world setting. The primary endpoint was HBsAg clearance after 3 years' follow-up. RESULTS: The modified intention-to-treat population comprised 844 hepatitis B e antigen (HBeAg)-positive patients (540 [64%] completed 3 years' follow-up), and 872 HBeAg-negative patients (614 [70%] completed 3 years' follow-up). At 3 years' follow-up, HBsAg clearance rates in HBeAg-positive and HBeAg-negative populations, respectively, were 2% (16/844) and 5% (41/872) in the modified intention-to-treat population and 5% [16/328] and 10% [41/394] in those with available data. In HBeAg-positive patients with data, Week 12 HBsAg levels <1500, 1500-20,000, and >20,000 IU/mL were associated with HBsAg clearance rates at 3 years' follow-up of 11%, 1%, and 5%, respectively (Week 24 predictability was similar). In HBeAg-negative patients with available data, a ≥10% decline vs a <10% decline in HBsAg at Week 12 was associated with HBsAg clearance rates of 16% vs 4%. Hepatocellular carcinoma incidence was lower than REACH-B (Risk Estimation for Hepatocellular Carcinoma in Chronic Hepatitis B) model predictions. CONCLUSIONS: Sustained off-treatment immune control is achieved with peginterferon alfa-2a in a real-world setting. HBsAg clearance 3 years after completion of peginterferon alfa-2a can be predicted on the basis of on-treatment HBsAg kinetics.
F Hoffmann La Roche Ltd Basel Switzerland
Gastroenterology and Hepatology Prince of Songkla University Songkhla Thailand
Gastroenterology and Hepatology Sungkyunkwan University School of Medicine Seoul South Korea
Gastroenterology and Hepatology University of Milan Milan Italy
Gastroenterology Hepatology and Endocrinology Hannover Medical School Hannover Germany
Gastroenterology Laiko General Hospital Athens Greece
Hepatologie Université Paris Diderot Clichy France
Infectious Disease and Hepatology Medical University of Białystok Białystok Poland
Infectious Diseases Ruijin Hospital Shanghai China
Liver Unit Asklepios Klinik St Georg Hamburg Germany
Liver Unit Queen Mary University of London London United Kingdom
PROMETRIS GmbH Mannheim Germany
Roche Pharma AG Grenzach Wyhlen Germany
Roche s r o Prague Czech Republic
Service d'Hepatologie Institut Arnault Tzanck Saint Laurent du Var France
References provided by Crossref.org
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