Evidence map›Paper›PMID 40087915›Full record

Trial reportJournal of viral hepatitis2025

Frequency, Severity and Impact of Pegylated Interferon Alpha-Associated Flares in Hepatitis D Infection.

Svenja Hardtke, Cihan Yurdaydin, Florin A Caruntu, Manuela G Curescu, Kendal Yalcin, Ulus S Akarca, Selim Gürel, Stefan Zeuzem, Andreas Erhardt, Stefan Lüth and 6 more

Registry-linked trialAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Journal of viral hepatitis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00932971 (A Multicenter Randomised Study Comparing the Efficacy of PegIFN-alfa2a Plus Placebo vs. PegIFN-alfa2a Plus Tenofovir for the Treatment of Chronic Delta Hepatitis-The Hep-Net International Delta Hepatitis Interventional Trial II), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT00932971 phase2completednot on this map

A Multicenter Randomised Study Comparing the Efficacy of PegIFN-alfa2a Plus Placebo vs. PegIFN-alfa2a Plus Tenofovir for the Treatment of Chronic Delta Hepatitis-The Hep-Net International Delta Hepatitis Interventional Trial II (HIDIT-II)

TypeinterventionalSponsorHepNet Study House, German LiverfoundationRan2009 to 2017Enrolled70ConditionsHepatitis DArmsPEG-IFN alfa-2a, Tenofovir, PEG-IFN alfa-2a, placebo
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Observational
  2. Article
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

16 authors.

Svenja HardtkeDepartment of Gastroenterology, Hepatology, Infectious Diseases, and Endocrinology, Hannover Medical School, Hannover, Germany.
Cihan YurdaydinDepartment of Gastroenterology, Ankara University Medical School, Ankara, Turkey.ORCID https://orcid.org/0000-0002-5419-7158
Florin A CaruntuInstitutul de Boli Infectioase, Bucharest, Romania.
Manuela G CurescuSpitalul Clinic de Boli Infectioase Si, Timisoara, Romania.
Kendal YalcinDicle University Medical Hospitals, Diyarbakir, Turkey.
Ulus S AkarcaEge University Medical Faculty Hospital, Izmir, Turkey.
Selim GürelUludağ University Medical School, Bursa, Turkey.
Stefan ZeuzemDepartment of Medicine, University Hospital, Goethe-University, Frankfurt, Germany.
Andreas ErhardtHeinrich Heine University, Düsseldorf, Germany.
Stefan LüthDepartment of Gastroenterology, Diabetology and Hepatology, University Hospital Brandenburg, Medical School (Theodor Fontane), Brandenburg, Germany.
George V PapatheodoridisFirst Department of Gastroenterology, Medical School, National and Kapodistrian University of Athens, General Hospital of Athens "Laiko", Athens, Greece.ORCID https://orcid.org/0000-0002-3518-4060
Kerstin PortDepartment of Gastroenterology, Hepatology, Infectious Diseases, and Endocrinology, Hannover Medical School, Hannover, Germany.
Michael P MannsDepartment of Gastroenterology, Hepatology, Infectious Diseases, and Endocrinology, Hannover Medical School, Hannover, Germany.
Markus CornbergDepartment of Gastroenterology, Hepatology, Infectious Diseases, and Endocrinology, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0002-9141-8001
Julia KahlhöferDepartment of Gastroenterology, Hepatology, Infectious Diseases, and Endocrinology, Hannover Medical School, Hannover, Germany.
Heiner WedemeyerDepartment of Gastroenterology, Hepatology, Infectious Diseases, and Endocrinology, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0003-2906-0480

Funding

F. Hoffmann-La RocheGilead SciencesHepNet Study-House (a project of the German Liver Foundation founded by the German Liver Foundation, the German Ministry for Education and Research, and the German Center for Infection Research)
6 · The paper itself

Abstract

We analysed the frequency, severity and impact of hepatitis flares in a large Phase 2 study investigating pegylated interferon-alfa-2a (PEG-IFNa) for the treatment of hepatitis D. In the HIDIT-II study, 120 patients were treated for 96 weeks with PEG-IFNa (180 μg weekly) in combination with tenofovir disoproxil fumarate (TDF, 300 mg once daily) or placebo. Hepatitis flares were defined as ALT increases above 10 times the upper limit of normal or increases of more than 2.5-fold above baseline or nadir values. ALT flares occurred in 28 patients (23%) during treatment (< 96) and in 14 patients post-treatment until follow-up Week 24. There were no differences in the flare frequency between the two treatment arms (12 PEG-IFNa + placebo vs. 16 PEG-IFNa + TDF). The frequency of ALT increases did not differ between cirrhotic and noncirrhotic patients. None of the patients with cirrhosis experienced liver decompensation during or after a flare. Fifty-four per cent of the patients with ALT flare experienced a decrease in HDV RNA (> 1 log10 cop/ml) during subsequent study visits. Mean ALT levels early during treatment were higher in patients with HBsAg loss at follow-up Week 24. More than a third of hepatitis D patients undergoing PEG-IFNa therapy may experience ALT flares during or after treatment. ALT flares in this study posed no obvious safety risk to patients and should not lead to premature withdrawal from treatment. If ALT flares may be beneficial in single patients requires further investigation. Clinical Trial Registration: NCT00932971, EudraCT 2008-005560-13.

Indexed as

Antiviral AgentsHepatitis DHepatitis D, ChronicInterferon-alphaPolyethylene GlycolsAdultAgedAlanine TransaminaseDrug Therapy, CombinationFemaleHumansMaleMiddle AgedPlacebosRecombinant ProteinsRNA, ViralAlanine TransaminaseAntiviral AgentsInterferon-alphapeginterferon alfa-2aPlacebosPolyethylene GlycolsRecombinant ProteinsRNA, ViralTenofoviralanine aminotransferasebeneficial flarescombination therapydeltaHDVhepatitis flaresHIDIT‐IIinterferonrandomised trialvirological outcome

Identifiers

PMID40087915
PMCPMC11909584

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Registered trials

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.