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DC Field | Value | Language |
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dc.contributor.author | Kaewdech A. | |
dc.contributor.author | Assawasuwannakit S. | |
dc.contributor.author | Sripongpun P. | |
dc.contributor.author | Chamroonkul N. | |
dc.contributor.author | Tangkijvanich P. | |
dc.contributor.author | Piratvisuth T. | |
dc.date.accessioned | 2022-12-14T03:17:48Z | - |
dc.date.available | 2022-12-14T03:17:48Z | - |
dc.date.issued | 2022 | |
dc.identifier.issn | 2296858X | |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85128219724&doi=10.3389%2ffmed.2022.859430&partnerID=40&md5=510fa9fbf00dc66895e910b5b4d4d278 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/27620 | - |
dc.description.abstract | Background: 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.language | en | |
dc.publisher | Frontiers Media S.A. | |
dc.subject | cessation | |
dc.subject | clinical relapse (CR) | |
dc.subject | hepatitis B core-related antigen (HBcrAg) | |
dc.subject | hepatitis B surface antigen (HBsAg) | |
dc.subject | hepatitis B virus ribonucleic acid (HBV RNA) | |
dc.subject | nucleos(t)ide analogues (NAs) | |
dc.subject | S-loss | |
dc.subject | SCALE-B | |
dc.title | Clinical 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.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Scientia Pharmaceutica. Vol 90, No.2 (2022) | |
dc.identifier.doi | 10.3389/fmed.2022.859430 | |
Appears in Collections: | Scopus 2022 |
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