Evidence map›Paper›PMID 40923770›Full record

ArticleJournal of viral hepatitis2025

Clinical Impact of Continuation Versus Cessation of Antiviral Therapy in Chronic Hepatitis B: A Modelling Study With Implications for Hepatitis B Cure.

Amir M Mohareb, Ghideon Ezaz, Arthur Y Kim, Kenneth A Freedberg, Anders Boyd, Emily P Hyle

Abstract read
In one paragraph

Article in Journal of viral hepatitis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Amir M MoharebMedical Practice Evaluation Center, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-3761-6154
Ghideon EzazIcahn School of Medicine at Mount Sinai, New York, New York, USA.
Arthur Y KimDivision of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
Kenneth A FreedbergMedical Practice Evaluation Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Anders BoydPublic Health Service of Amsterdam, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0001-9512-8928
Emily P HyleMedical Practice Evaluation Center, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-8721-106X

Funding

Optimizing HIV Care in Less Developed CountriesR01AI058736 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Kenneth Alan Freedberg, Emily Parker Hyle · 2004 to 2026
$21.5M
Optimizing HIV Care in Less Developed CountriesR37AI058736 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI FREEDBERG, KENNETH ALAN · 2018 to 2024
$6.6M
Simulation Modeling of Hepatitis B Virus Elimination Strategies in Cote d'IvoireK01AI166126 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Amir Mohareb · 2022 to 2026
$679k
NIAID NIH HHS K01 AI166126NIAID NIH HHS R01 AI058736NIAID NIH HHS R37 AI058736NIH HHS K01AI166126NIH HHS R37AI058736
6 · The paper itself

Abstract

Discontinuing antivirals in chronic hepatitis B virus (HBV) 'e' antigen negative infection can enhance HBV surface antigen (HBsAg) loss but risks complications. We modelled the clinical impact of discontinuing antivirals in chronic HBV. We developed a Markov state model with Monte Carlo simulation of chronic HBV to compare continuation of antiviral therapy with 3 strategies of cessation and reinitiation for: (1) virologic relapse, (2) clinical relapse, or (3) hepatitis flare. We simulated the probability of virologic relapse as an exponential decay function from the time of antiviral cessation. We used literature-based estimates for input probabilities following virologic relapse: clinical relapse (60%, conditional on virologic relapse), hepatitis flare (57%, conditional on clinical relapse) and HBsAg-loss (6%-8%). We projected HBsAg loss, cirrhosis, HCC, and survival. In 10 years, cessation strategies would increase cumulative incidence of HBsAg loss from 4.6% to 12.9%-17.3% but would not appreciably change survival (from 90.6% with continuation to 88.1%-89.0%). In an undifferentiated population, continuation would be a preferred strategy to increase average life expectancy (by 0.75-1.05 years) unless HBsAg loss following treatment cessation was > 46%. Sensitivity analyses showed that the decision to continue or stop antivirals would depend on the off-treatment rates of cirrhosis and HCC for people who remain HBsAg-positive but do not fulfil retreatment criteria. Careful selection of people for antiviral cessation using quantitative HBsAg levels could improve survival compared with continuation. Clinical practice guidelines should emphasise selective application of antiviral cessation to persons most likely to lose HBsAg without experiencing liver-related complications.

Indexed as

Antiviral AgentsHepatitis B, ChronicWithholding TreatmentAdultCarcinoma, HepatocellularFemaleHepatitis B Surface AntigensHumansLiver CirrhosisLiver NeoplasmsMaleMarkov ChainsMiddle AgedMonte Carlo MethodRecurrenceSurvival AnalysisAntiviral AgentsHepatitis B Surface Antigensantiviral therapycirrhosishepatitis B virushepatitis flarereactivation

Identifiers

PMID40923770
PMCPMC12444364

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.