Durability of Hepatitis B Surface Antigen Loss With Nucleotide Analogue and Peginterferon Therapy in Patients With Chronic Hepatitis B.


Journal

Hepatology communications
ISSN: 2471-254X
Titre abrégé: Hepatol Commun
Pays: United States
ID NLM: 101695860

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 12 07 2019
accepted: 07 09 2019
entrez: 8 1 2020
pubmed: 8 1 2020
medline: 8 1 2020
Statut: epublish

Résumé

In patients with chronic hepatitis B (CHB), loss of hepatitis B surface antigen (HBsAg) is considered a functional cure. However, HBsAg loss is uncommon with existing therapies, and predictive factors associated with HBsAg seroreversion are unknown. Using pooled data from three phase 3 clinical trials of patients with CHB treated with nucleos(t)ide analogue (NUC) monotherapy or peginterferon (Peg-IFN) ± NUC combination therapy, we conducted a retrospective analysis to characterize patients who achieved sustained HBsAg loss, the predictors of HBsAg seroreversion, and the impact of hepatitis B surface antibody (anti-HBs) seroconversion on durability of HBsAg loss. In these three international trials, 1,381 adults with CHB received either NUC monotherapy for up to 10 years or Peg-IFN-containing regimens for up to 1 year. A total of 55 patients had confirmed HBsAg loss, defined as two or more consecutive negative-qualitative HBsAg results, with a minimum of one repeat result after the end of treatment. Throughout a median of 96 (quartile [Q]1, Q3, 46, 135) weeks follow-up after HBsAg loss, HBsAg loss was durable in 82% (n = 45) of patients, with 10 patients experiencing HBsAg seroreversion. Anti-HBs seroconversion was observed during follow-up in 78% of patients who lost HBsAg and in 60% of those who subsequently seroreverted. In analyzing predictors of HBsAg seroreversion, study treatment was significant, yet anti-HBs seroconversion and treatment duration after initial HBsAg loss were not. Risk of HBsAg seroreversion was observed to be lower if HBsAg loss was sustained through the off-treatment week 24 visit (8/10 seroreversions occurred by posttreatment week 24).

Identifiants

pubmed: 31909352
doi: 10.1002/hep4.1436
pii: HEP41436
pmc: PMC6939500
doi:

Types de publication

Journal Article

Langues

eng

Pagination

8-20

Informations de copyright

© 2019 The Authors. Hepatology Communications published by Wiley Periodicals, Inc., on behalf of the American Association for the Study of Liver Diseases.

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Auteurs

Anna S Lok (AS)

University of Michigan Ann Arbor MI.

Fabien Zoulim (F)

Hospices Civils de Lyon and INSERM Unit 1052 Lyon France.

Geoffrey Dusheiko (G)

Kings College Hospital University College London Medical School London United Kingdom.

Henry L Y Chan (HLY)

Chinese University of Hong Kong Hong Kong S.A.R.

Maria Buti (M)

Vall d'Hebron Hospital Barcelona Spain.

Marc G Ghany (MG)

National Institutes of Health Bethesda MD.

Anuj Gaggar (A)

Gilead Sciences, Inc. Foster City CA.

Jenny C Yang (JC)

Gilead Sciences, Inc. Foster City CA.

George Wu (G)

Gilead Sciences, Inc. Foster City CA.

John F Flaherty (JF)

Gilead Sciences, Inc. Foster City CA.

G Mani Subramanian (GM)

Gilead Sciences, Inc. Foster City CA.

Stephen Locarnini (S)

Victorian Infectious Diseases Reference Laboratory Melbourne Australia.

Patrick Marcellin (P)

Hôpital Beaujon Université de Paris Diderot Clichy France.

Classifications MeSH