Evidence map›Paper›PMID 42522680›Full record

ArticleJournal of viral hepatitis2026

Differential Hepatitis B Surface Antigen Glycan Isomer Kinetics Between Tenofovir Alafenamide and Entecavir: Hepatocellular Carcinoma Risk Stratification in Hepatitis B e Antigen-Positive Patients.

Yuji Kita, Ayato Murata, Hiroki Nago, Masahiro Yamaguchi, Yoko Kato, Rihwa Om, Yuichro Terai, Yuji Ikeda, Sho Sato, Shunsuke Sato and 2 more

Abstract read
In one paragraph

Article in Journal of viral hepatitis, 2026. 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

12 authors.

Yuji KitaDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
Ayato MurataDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
Hiroki NagoDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
Masahiro YamaguchiDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
Yoko KatoDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
Rihwa OmDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
Yuichro TeraiDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
Yuji IkedaDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
Sho SatoDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
Shunsuke SatoDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.ORCID https://orcid.org/0000-0002-7480-7283
Yuji ShimadaDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.ORCID https://orcid.org/0000-0003-1648-7565
Takuya GendaDepartment of Gastroenterology and Hepatology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.ORCID https://orcid.org/0000-0003-0006-8948

Funding

JIMROOtsuka PharmaceuticalTaiho Pharma
6 · The paper itself

Abstract

Nucleos(t)ide analog (NA) therapy suppresses hepatitis B virus (HBV) DNA, but residual hepatocellular carcinoma (HCC) risk persists. O-glycosylated hepatitis B surface antigen glycan isomer (HBsAgGi) uniquely reflects virion burden. We evaluated the impact of tenofovir alafenamide (TAF) versus entecavir (ETV) on 48-week HBsAgGi kinetics and its utility in stratifying HCC risk in 90 NA-naïve patients (ETV: 73; TAF: 17). A favourable response was defined as a reduction or maintenance of low HBsAgGi levels. TAF independently predicted a favourable response compared with ETV (penalised odds ratio 3.60, p = 0.030). A significant interaction occurred between HBeAg status and HBsAgGi response in relation to HCC development (p = 0.038). In HBeAg-positive patients, a poor response was associated with increased HCC risk (hazard ratio 7.34, 95% confidence interval [CI] 1.96-20.35, p = 0.001); however, the exact magnitude warrants cautious interpretation due to wide CIs. This association was absent in HBeAg-negative cases. Adding HBsAgGi response to the aMAP score improved long-term HCC prediction exclusively in the HBeAg-positive cohort. As the assay targets genotype C-specific O-glycosylation, the findings cannot be generalised to genotypes A, B, or D. In conclusion, on-treatment HBsAgGi response is a specific surrogate marker for stratifying residual HCC risk in HBeAg-positive patients, and TAF is more effective than ETV in inducing these favourable kinetics.

Indexed as

AdenineAntiviral AgentsCarcinoma, HepatocellularGuanineHepatitis B, ChronicHepatitis B e AntigensHepatitis B Surface AntigensLiver NeoplasmsPolysaccharidesTenofovirAdultAgedAlanineFemaleHepatitis B virusHumansAdenineAlanineAntiviral AgentsentecavirGuanineHepatitis B e AntigensHepatitis B Surface AntigensPolysaccharidesTenofovirtenofovir alafenamideantiviral agentsbiomarkerschronic hepatitis Bhepatocellular carcinomarisk assessment

Identifiers

PMID42522680
PMCPMC13417045

What OpenQuestion holds

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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.