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Hepatitis B surface antigen titer is a good indicator of durable viral response after entecavir off-treatment for chronic hepatitis B

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dc.contributor.authorLee, Han Ah-
dc.contributor.authorSeo, Yeon Seok-
dc.contributor.authorPark, Seung Woon-
dc.contributor.authorPark, Sang Jung-
dc.contributor.authorKim, Tae Hyung-
dc.contributor.authorSuh, Sang Jun-
dc.contributor.authorJung, Young Kul-
dc.contributor.authorKim, Ji Hoon-
dc.contributor.authorAn, Hyunggin-
dc.contributor.authorYim, Hyung Joon-
dc.contributor.authorYeon, Jong Eun-
dc.contributor.authorByun, Kwan Soo-
dc.contributor.authorUm, Soon Ho-
dc.date.accessioned2021-09-03T20:33:30Z-
dc.date.available2021-09-03T20:33:30Z-
dc.date.created2021-06-16-
dc.date.issued2016-09-
dc.identifier.issn2287-2728-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/87670-
dc.description.abstractBackground/Aims: Clear indicators for stopping antiviral therapy in chronic hepatitis B (CHB) patients are not yet available. Since the level of hepatitis B surface antigen (HBsAg) is correlated with covalently closed circular DNA, the HBsAg titer might be a good indicator of the off-treatment response. This study aimed to determine the relationship between the HBsAg titer and the entecavir (ETV) off-treatment response. Methods: This study analyzed 44 consecutive CHB patients (age, 44.6 +/- 11.4 years, mean +/- SD; men, 63.6%; positive hepatitis B envelope antigen (HBeAg) at baseline, 56.8%; HBV DNA level, 6.8 +/- 1.3 log(10) IU/mL) treated with ETV for a sufficient duration and in whom treatment was discontinued after HBsAg levels were measured. A virological relapse was defined as an increase in serum HBV DNA level of >2000 IU/mL, and a clinical relapse was defined as a virological relapse with a biochemical flare, defined as an increase in the serum alanine aminotransferase level of >2 x upper limit of normal. Results: After stopping ETV, virological relapse and clinical relapse were observed in 32 and 24 patients, respectively, during 20.8 +/- 19.9 months of follow-up. The cumulative incidence rates of virological relapse were 36.2% and 66.2%, respectively, at 6 and 12 months, and those of clinical relapse were 14.3% and 42.3%. The off-treatment HBsAg level was an independent factor associated with clinical relapse (hazard ratio, 2.251; 95% confidence interval, 1.076-4.706; P=0.031). When patients were grouped according to off-treatment HBsAg levels, clinical relapse did not occur in patients with an off-treatment HBsAg level of <= 2 log(10) IU/mL (n=5), while the incidence rates of clinical relapse at 12 months after off-treatment were 28.4% and 55.7% in patients with off-treatment HBsAg levels of >2 and <= 3 log(10) IU/mL (n=11) and >3 log(10) IU/mL (n=28), respectively. Conclusions: The off-treatment HBsAg level is closely related to clinical relapse after treatment cessation. A serum HBsAg level of <2 log(10) IU/mL is an excellent predictor of a sustained off-treatment response in CHB patients who have received ETV for a sufficient duration.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN ASSOC STUDY LIVER-
dc.subjectHBEAG SEROCONVERSION-
dc.subjectANTIVIRAL THERAPY-
dc.subjectVIROLOGICAL RESPONSE-
dc.subjectTREATMENT CESSATION-
dc.subjectLAMIVUDINE THERAPY-
dc.subjectADEFOVIR DIPIVOXIL-
dc.subjectNATURAL-HISTORY-
dc.subjectVIRUS INFECTION-
dc.subjectOPEN-LABEL-
dc.subjectDURABILITY-
dc.titleHepatitis B surface antigen titer is a good indicator of durable viral response after entecavir off-treatment for chronic hepatitis B-
dc.typeArticle-
dc.contributor.affiliatedAuthorSeo, Yeon Seok-
dc.contributor.affiliatedAuthorByun, Kwan Soo-
dc.identifier.doi10.3350/cmh.2016.0047-
dc.identifier.scopusid2-s2.0-85014868101-
dc.identifier.wosid000407832900010-
dc.identifier.bibliographicCitationCLINICAL AND MOLECULAR HEPATOLOGY, v.22, no.3, pp.382 - 389-
dc.relation.isPartOfCLINICAL AND MOLECULAR HEPATOLOGY-
dc.citation.titleCLINICAL AND MOLECULAR HEPATOLOGY-
dc.citation.volume22-
dc.citation.number3-
dc.citation.startPage382-
dc.citation.endPage389-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART002145396-
dc.description.journalClass1-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusHBEAG SEROCONVERSION-
dc.subject.keywordPlusANTIVIRAL THERAPY-
dc.subject.keywordPlusVIROLOGICAL RESPONSE-
dc.subject.keywordPlusTREATMENT CESSATION-
dc.subject.keywordPlusLAMIVUDINE THERAPY-
dc.subject.keywordPlusADEFOVIR DIPIVOXIL-
dc.subject.keywordPlusNATURAL-HISTORY-
dc.subject.keywordPlusVIRUS INFECTION-
dc.subject.keywordPlusOPEN-LABEL-
dc.subject.keywordPlusDURABILITY-
dc.subject.keywordAuthorHepatitis B virus-
dc.subject.keywordAuthorHepatitis B surface antigen-
dc.subject.keywordAuthorRelapse-
dc.subject.keywordAuthorOff-treatment-
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