Evidence map›Paper›PMID 42256228›Full record

Observational studyFrontiers in cellular and infection microbiology2026

HBsAg loss in chronic hepatitis B patients with an HBsAg decline plateau can be enhanced by intermittent PEG-IFN treatment.

Weihua Cao, Si Xie, Hongxiao Hao, Wen Deng, Lu Zhang, Yao Lu, Ruyu Liu, Shiyu Wang, Xinxin Li, Ziyu Zhang and 10 more

Abstract readObservational Study
In one paragraph

Observational study in Frontiers in cellular and infection microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

20 authors.

Weihua Cao *Department of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Si Xie *Division of Hepatology, Hepato-Pancreato-Biliary Center, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University, Beijing, China.
Hongxiao Hao *Department of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Wen Deng *Department of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Lu ZhangDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Yao LuDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Ruyu LiuDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Shiyu WangDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Xinxin LiDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Ziyu ZhangDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Xin WeiDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Zixuan GaoDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Linmei YaoDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Shuojie WangDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Yuanjiao GaoDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Yujie WangDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Mengjiao XuDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Leiping HuDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Yao XieDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Minghui LiDepartment of Hepatology Division 2, Beijing Ditan Hospital, Capital Medical University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: During interferon (IFN) treatment patients with chronic hepatitis B (CHB), HBsAg levels often declines to a plateau. This study investigated the HBsAg loss rate in patients receiving continuous IFN treatment after reaching a plateau compared with patients who suspended IFN treatment for 3-6 months. Methods: Patients were enrolled from an observational cohort of CHB patients receiving PEG-IFN-α-based therapy. All patients reached a plateau in qHBsAg decline after 24 weeks of PEG-IFN-α treatment. Patients in the continuous-treatment group received continuous PEG-IFN therapy, while patients in the intermittent-treatment group discontinued initial PEG-IFN therapy for 3-6 months before resuming treatment. Results: In this retrospective study, 403 CHB patients with a plateau in HBsAg decline after 24 weeks of pegylated IFN-α (PEG-IFN-α) treatment were included. After reaching the plateau, patients either continued PEG-IFN treatment or restarted treatment after an interval. The HBsAg loss rate in the intermittent-treatment group was significantly higher than that in the continuous-treatment group (p = 0.001); in the 278-case propensity score matching (PSM) population, HBsAg loss rates were 21.58% and 8.63%, respectively (p = 0.002). Multivariate Cox regression analysis showed that intermittent therapy (p = 0.017) and HBsAg level at the second plateau time point (p < 0.001) were independent factors of HBsAg loss. Multivariate Cox regression analysis of the PSM-matched population showed that baseline HBsAg level (p = 0.043), HBsAg level at the second plateau time point (p = 0.000), and intermittent therapy (p = 0.004) were independent factors of HBsAg loss. Conclusions: Among CHB patients receiving PEG-IFN-based treatment, intermittent treatment was more beneficial than continuous treatment in achieving HBsAg loss once HBsAg decline reached a plateau.

Indexed as

Antiviral AgentsHepatitis B, ChronicHepatitis B Surface AntigensInterferon-alphaPolyethylene GlycolsAdultFemaleHumansMaleMiddle AgedRecombinant ProteinsRetrospective StudiesTreatment OutcomeAntiviral AgentsHepatitis B Surface AntigensInterferon-alphapeginterferon alfa-2aPolyethylene GlycolsRecombinant Proteinsantiviral therapychronic hepatitis BHBsAg lossintermittent therapypegylated interferon

Identifiers

PMID42256228
PMCPMC13233439

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Registered trials

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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.