Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/27620
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dc.contributor.authorKaewdech A.
dc.contributor.authorAssawasuwannakit S.
dc.contributor.authorSripongpun P.
dc.contributor.authorChamroonkul N.
dc.contributor.authorTangkijvanich P.
dc.contributor.authorPiratvisuth T.
dc.date.accessioned2022-12-14T03:17:48Z-
dc.date.available2022-12-14T03:17:48Z-
dc.date.issued2022
dc.identifier.issn2296858X
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85128219724&doi=10.3389%2ffmed.2022.859430&partnerID=40&md5=510fa9fbf00dc66895e910b5b4d4d278
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/27620-
dc.description.abstractBackground: Discontinuation of antiviral therapy in chronic hepatitis B (CHB) patients leads to a higher hepatitis B surface antigen (HBsAg) loss; yet, clinical relapse (CR) may occur. SCALE-B score was developed to predict off-treatment CR; however, validation of SCALE-B beyond a 48-week follow-up is rare. We studied whether SCALE-B and hepatitis B virus ribonucleic acid (HBV RNA) could predict outcomes in CHB patients after a 2-year follow-up. Methods: A total of 92 Thai CHB patients who stopped antiviral treatment were followed up; baseline characteristics, quantitative hepatitis B surface antigen (qHBsAg), hepatitis B core-related antigen (HBcrAg), and HBV RNA were collected at the time of discontinuation, and SCALE-B scores were calculated. Patients were followed up every 12 weeks for 48 weeks, and then, the intervals were upon primary doctors. Follow-up data regarding virological relapse (VR), CR, and HBsAg loss were obtained. Results: The median follow-up duration was 142 weeks; the cumulative incidences of VR, CR, and HBsAg loss were 65.2, 33.7, and 7.6%, respectively. After 48 weeks, VR and CR plateaued, but HBsAg loss increased from 2.2 to 7.6%. According to the SCALE-B strata, VR, CR, and HBsAg loss were significantly different. The highest stratum (≥ 320) was associated with higher VR, CR, and lesser HBsAg loss when compared to the lowest stratum, with adjusted hazard ratios of 5.0 (95% CIs: 1.8–14.4), 10.44 (95% CIs: 1.4–79.1), and 0.04 (95% CIs: 0.004–0.43), respectively. Conclusion: At a median follow-up of 2.5 years after discontinuing therapy, HBsAg loss in Thai patients was found to increase over time. SCALE-B is a valuable tool for predicting CR, VR, and HBsAg loss; HBV RNA is not significantly associated with long-term outcomes. Clinical Trial Registration: [www.ClinicalTrials.gov], identifier [TCTR20180316007]. Copyright © 2022 Kaewdech, Assawasuwannakit, Sripongpun, Chamroonkul, Tangkijvanich and Piratvisuth.
dc.languageen
dc.publisherFrontiers Media S.A.
dc.subjectcessation
dc.subjectclinical relapse (CR)
dc.subjecthepatitis B core-related antigen (HBcrAg)
dc.subjecthepatitis B surface antigen (HBsAg)
dc.subjecthepatitis B virus ribonucleic acid (HBV RNA)
dc.subjectnucleos(t)ide analogues (NAs)
dc.subjectS-loss
dc.subjectSCALE-B
dc.titleClinical Utility of SCALE-B to Predict Hepatitis B Virus Relapse, Hepatitis B Surface Antigen Loss After Antiviral Cessation in Asian Patients After 2-Year Follow-up
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationScientia Pharmaceutica. Vol 90, No.2 (2022)
dc.identifier.doi10.3389/fmed.2022.859430
Appears in Collections:Scopus 2022

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