Outcome of nucleos(t)ide analog intervention in patients with preventive or on-demand therapy for hepatitis B virus reactivation.


Journal

Journal of medical virology
ISSN: 1096-9071
Titre abrégé: J Med Virol
Pays: United States
ID NLM: 7705876

Informations de publication

Date de publication:
06 2021
Historique:
revised: 24 08 2020
received: 15 07 2020
accepted: 26 08 2020
pubmed: 18 9 2020
medline: 9 10 2021
entrez: 17 9 2020
Statut: ppublish

Résumé

Preventive or on-demand nucleos(t)ide analog (NA) therapy can prevent severe hepatitis related to hepatitis B virus reactivation (HBV-R). However, it is unclear if NA can be safely stopped in such patients after cytotoxic therapies or during immunosuppressive therapies. We retrospectively evaluated 133 patients who initiated NA therapy between 2007 and 2018. A total of 103 patients were positive for HBV surface antigen (HBsAg) at baseline, and NA therapy was started before cytotoxic or immunosuppressive therapy (preventive group). Thirty patients with resolved HBV infection were treated with NA therapy after HBV reactivation (on-demand group). Virological relapse was defined as a serum HBV DNA level >20 IU/ml. NA therapy was stopped in 12 (12%) patients (preventive group), and in 16 (53%) patients (on-demand group). After the cessation of NA therapy, the cumulative rates of relapse were 36% and 39% at 12 and 24 months, respectively. High levels of HBsAg both at baseline and at the cessation of NA therapy were related to the occurrence of relapse. Relapse did not occur in patients with HBsAg levels <20 IU/ml (preventive group). HBV relapse occurred in five (33%) patients in the on-demand group. Relapse occurred only in anti-HBs-negative patients at the cessation of NA therapy. There were no cases of hepatitis flare after the cessation of NA therapy. HBsAg predicted HBV relapse after the cessation of NA therapy in HBsAg-positive patients. Anti-HBs could be a predictive marker for NA therapy cessation in patients with resolved HBV.

Identifiants

pubmed: 32940921
doi: 10.1002/jmv.26526
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0
Nucleosides 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3679-3687

Informations de copyright

© 2020 Wiley Periodicals LLC.

Références

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Auteurs

Akihiro Tamori (A)

Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.

Kiminori Kimura (K)

Department of Hepatology, Tokyo Metropolitan Komagome Hospital, Tokyo, Japan.

Kiyohide Kioka (K)

Department of Hepatology, Osaka City General Hospital, Osaka, Japan.

Hirayuki Enomoto (H)

Department of Internal Medicine, Division of Gastroenterology and Hepatology, Hyogo College of Medicine, Nishinomiya, Japan.

Naoshi Odagiri (N)

Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.

Ritsuzo Kozuka (R)

Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.

Sawako Uchida-Kobayashi (S)

Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.

Masaru Enomoto (M)

Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.

Norifumi Kawada (N)

Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.

Masashi Mizokami (M)

Genome Medical Sciences Project, National Center for Global Health and Medicine, Tokyo, Japan.

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