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Discontinuation of nucleos(t)ide analogues is not associated with a higher risk of HBsAg seroreversion after antiviral-induced HBsAg seroclearance: a nationwide multicentre study

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dc.contributor.authorKim, Minseok Albert-
dc.contributor.authorKim, Seung Up-
dc.contributor.authorSinn, Dong Hyun-
dc.contributor.authorJang, Jeong Won-
dc.contributor.authorLim, Young-Suk-
dc.contributor.authorAhn, Sang Hoon-
dc.contributor.authorShim, Jae-Jun-
dc.contributor.authorSeo, Yeon Seok-
dc.contributor.authorBaek, Yang Hyun-
dc.contributor.authorKim, Sang Gyune-
dc.contributor.authorKim, Young Seok-
dc.contributor.authorKim, Ji Hoon-
dc.contributor.authorChoe, Won Hyeok-
dc.contributor.authorYim, Hyung Joon-
dc.contributor.authorLee, Hyun Woong-
dc.contributor.authorKwon, Jung Hyun-
dc.contributor.authorLee, Sung Won-
dc.contributor.authorJang, Jae Young-
dc.contributor.authorKim, Hwi Young-
dc.contributor.authorPark, Yewan-
dc.contributor.authorKim, Gi-Ae-
dc.contributor.authorYang, Hyun-
dc.contributor.authorLee, Han Ah-
dc.contributor.authorKoh, Myeongseok-
dc.contributor.authorLee, Young-Sun-
dc.contributor.authorKim, Minkoo-
dc.contributor.authorChang, Young-
dc.contributor.authorKim, Yoon Jun-
dc.contributor.authorYoon, Jung-Hwan-
dc.contributor.authorZoulim, Fabien-
dc.contributor.authorLee, Jeong-Hoon-
dc.date.available2021-02-15T01:14:20Z-
dc.date.issued2020-12-
dc.identifier.issn0017-5749-
dc.identifier.issn1468-3288-
dc.identifier.urihttps://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/49204-
dc.description.abstractObjective Direct comparison of the clinical outcomes between nucleos(t)ide analogue (NA) discontinuation versus NA continuation has not been performed in patients with chronic hepatitis B who achieved HBsAg-seroclearance. Whether NA discontinuation was as safe as NA continuation after NA-induced surface antigen of HBV (HBsAg) seroclearance was investigated in the present study. Designs This multicentre study included 276 patients from 16 hospitals in Korea who achieved NA-induced HBsAg seroclearance: 131 (47.5%) discontinued NA treatment within 6 months after HBsAg seroclearance (NA discontinuation group) and 145 (52.5%) continued NA treatment (NA continuation group). Primary endpoint was HBsAg reversion and secondary endpoints included serum HBV DNA redetection and development of hepatocellular carcinoma (HCC). Results During follow-up (median=26.9 months, IQR=12.2-49.2 months), 10 patients (3.6%) experienced HBsAg reversion, 6 (2.2%) showed HBV DNA redetection and 8 (2.9%) developed HCC. Compared with NA continuation, NA discontinuation was not associated with HBsAg reversion in both univariable (HR=0.45, 95% CI=0.12 to 1.76, log-rank p=0.24) and multivariable analyses (adjusted HR=0.65, 95% CI=0.16 to 2.59, p=0.54). The cumulative probabilities of HBsAg reversion at 1, 3 and 5 years were 0.8%, 2.3% and 5.0% in the NA discontinuation group, and 1.5%, 6.3% and 8.4% in the NA continuation group, respectively. NA discontinuation was not associated with higher risk of either HBV redetection (HR=0.83, 95% CI=0.16 to 4.16, log-rank p=0.82) or HCC development (HR=0.53, 95% CI=0.12 to 2.23, log-rank p=0.38). Conclusion The discontinuation of NA was not associated with a higher risk of either HBsAg reversion, serum HBV DNA redetection or HCC development compared with NA continuation among patients who achieved HBsAg seroclearance with NA.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherBMJ Publishing Group-
dc.titleDiscontinuation of nucleos(t)ide analogues is not associated with a higher risk of HBsAg seroreversion after antiviral-induced HBsAg seroclearance: a nationwide multicentre study-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1136/gutjnl-2019-320015-
dc.identifier.scopusid2-s2.0-85082521120-
dc.identifier.wosid000591525700017-
dc.identifier.bibliographicCitationGut, v.69, no.12, pp 2214 - 2222-
dc.citation.titleGut-
dc.citation.volume69-
dc.citation.number12-
dc.citation.startPage2214-
dc.citation.endPage2222-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusCHRONIC HEPATITIS-B-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA-
dc.subject.keywordPlusENTECAVIR THERAPY-
dc.subject.keywordPlusSURFACE-ANTIGEN-
dc.subject.keywordPlusREDUCED RISK-
dc.subject.keywordPlusVIRUS-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordAuthorantivirals-
dc.subject.keywordAuthorHBsAg-
dc.subject.keywordAuthorHBV DNA redetection-
dc.subject.keywordAuthorhepatocellular carcinoma-
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