<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-19T16:08:42Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/8136" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/8136</identifier><datestamp>2025-10-24T10:22:52Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378092</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Probability of HBsAg loss after nucleo(s)tide analogue withdrawal depends on HBV genotype and viral antigen levels</dc:title>
   <dc:creator>Chiu, Shao-Ming</dc:creator>
   <dc:creator>Seto, Wai-Kay</dc:creator>
   <dc:creator>Sonneveld, Milan</dc:creator>
   <dc:creator>Brakenhoff, Sylvia</dc:creator>
   <dc:creator>Kaewdech, Apichat</dc:creator>
   <dc:creator>Park, Jun Yong</dc:creator>
   <dc:creator>Buti Ferret, Maria</dc:creator>
   <dc:subject>Medicaments antivírics - Ús terapèutic</dc:subject>
   <dc:subject>Hepatitis B - Tractament</dc:subject>
   <dc:subject>CHEMICALS AND DRUGS::Chemical Actions and Uses::Pharmacologic Actions::Therapeutic Uses::Anti-Infective Agents::Antiviral Agents</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::/therapeutic use</dc:subject>
   <dc:subject>DISEASES::Virus Diseases::DNA Virus Infections::Hepadnaviridae Infections::Hepatitis B::Hepatitis B, Chronic</dc:subject>
   <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::acciones y usos químicos::acciones farmacológicas::usos terapéuticos::antiinfecciosos::antivíricos</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::/uso terapéutico</dc:subject>
   <dc:subject>ENFERMEDADES::virosis::infecciones por virus ADN::infecciones por Hepadnaviridae::hepatitis B::hepatitis B crónica</dc:subject>
   <dcterms:abstract>HBV genotype; Viral antigen</dcterms:abstract>
   <dcterms:abstract>Genotipo VHB; Antígeno viral</dcterms:abstract>
   <dcterms:abstract>Genotip del VHB; Antigen viral</dcterms:abstract>
   <dcterms:abstract>Background &amp; Aims&#xd;
Nucleo(s)tide analogue (NUC) withdrawal may result in HBsAg clearance in a subset of patients. However, predictors of HBsAg loss after NUC withdrawal remain ill-defined.&#xd;
Methods&#xd;
We studied predictors of HBsAg loss in a global cohort of HBeAg-negative patients with undetectable HBV DNA who discontinued long-term NUC therapy. Patients requiring retreatment after treatment cessation were considered non-responders.&#xd;
Results&#xd;
We enrolled 1,216 patients (991 with genotype data); 98 (8.1%) achieved HBsAg loss. The probability of HBsAg loss was higher in non-Asian patients (adjusted hazard ratio [aHR] 8.26, p &lt;0.001), and in patients with lower HBsAg (aHR 0.243, p &lt;0.001) and HBV core-related antigen (HBcrAg) (aHR 0.718, p = 0.001) levels. Combining HBsAg (&lt;10, 10-100 or >100 IU/ml) and HBcrAg (&lt;2log vs. ≥2 log) levels improved prediction of HBsAg loss, with extremely low rates observed in patients with HBsAg >100 IU/ml with detectable HBcrAg. HBsAg loss rates also varied with HBV genotype; the highest rates were observed for genotypes A and D, and none of the patients with HBV genotype E experienced HBsAg loss (p &lt;0.001 for the overall comparison across genotypes; p &lt;0.001 for genotypes A/D vs. genotypes B/C). HBV genotype C was independently associated with a higher probability of HBsAg loss when compared to genotype B among Asian patients (aHR 2.494; 95% CI 1.490–4.174, p = 0.001).&#xd;
Conclusions&#xd;
The probability of HBsAg loss after NUC cessation varies according to patient ethnicity, HBV genotype and end-of-treatment viral antigen levels. Patients with low HBsAg (&lt;100 IU/ml) and/or undetectable HBcrAg levels, particularly if non-Asian or infected with HBV genotype C, appear to be the best candidates for treatment withdrawal.</dcterms:abstract>
   <dcterms:abstract>The CREATE study was supported by Fujirebio. No additional funding was obtained for this follow-up analysis.</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-24T10:22:52Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-24T10:22:52Z</dcterms:available>
   <dcterms:created>2025-10-24T10:22:52Z</dcterms:created>
   <dcterms:issued>2022-09-12T08:18:44Z</dcterms:issued>
   <dcterms:issued>2022-09-12T08:18:44Z</dcterms:issued>
   <dcterms:issued>2022-05</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/11351/8136</dc:identifier>
   <dc:relation>Journal of Hepatology;76(5)</dc:relation>
   <dc:relation>https://doi.org/10.1016/j.jhep.2022.01.007</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Elsevier</dc:publisher>
   <dc:source>Scientia</dc:source>
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