Chronic hepatitis B: a scoping review on the guidelines for stopping nucleos(t)ide analogue therapy.


Journal

Expert review of gastroenterology & hepatology
ISSN: 1747-4132
Titre abrégé: Expert Rev Gastroenterol Hepatol
Pays: England
ID NLM: 101278199

Informations de publication

Date de publication:
May 2023
Historique:
medline: 17 5 2023
pubmed: 28 3 2023
entrez: 27 3 2023
Statut: ppublish

Résumé

Nucleos(t)ide analogues (NAs) are effective in suppressing the replication of the hepatitis B virus. However, NAs cannot effectively induce hepatitis B surface antigen (HBsAg) seroclearance, which represents the optimal treatment endpoint in chronic hepatitis B (CHB). Hence, most CHB patients are advised for indefinite NA therapy, but recent data has supported the concept of finite NA therapy before HBsAg seroclearance. This article covered the latest evidence on stopping NAs in CHB, with a focused analysis on international guidelines. Articles were retrieved by a literature search on PubMed with the keywords 'chronic hepatitis B,' 'antiviral therapy,' 'nucleos(t)ide analogue,' 'cessation,' 'stopping', and 'finite.' Studies up till 1 December 2022 were included. Finite NA therapy in CHB has the potential in enhancing HBsAg seroclearance, however it also carries rare but potentially severe risks. NA cessation before HBsAg seroclearance is only suitable for a highly selected group of patients, whereas the majority of CHB patients should be treated indefinitely or until HBsAg seroclearance. Current guidelines have provided recommendations on stopping NAs, but further research is required to optimize the monitoring and retreatment protocol after stopping NAs.

Identifiants

pubmed: 36972516
doi: 10.1080/17474124.2023.2196405
doi:

Substances chimiques

Hepatitis B Surface Antigens 0
Antiviral Agents 0
DNA, Viral 0
Hepatitis B e Antigens 0

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

443-450

Auteurs

Rex Wan-Hin Hui (RW)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Hong Kong, China.

Lung-Yi Mak (LY)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Hong Kong, China.
State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong, China.

Wai-Kay Seto (WK)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Hong Kong, China.
State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong, China.

Man-Fung Yuen (MF)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Hong Kong, China.
State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong, China.

James Fung (J)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Hong Kong, China.

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Classifications MeSH