0 601

Cited 23 times in

Cited 24 times in

Negligible HCC risk during stringently defined untreated immune-tolerant phase of chronic hepatitis B

DC Field Value Language
dc.contributor.authorLee, Hye Won-
dc.contributor.authorChon, Young Eun-
dc.contributor.authorKim, Beom Kyung-
dc.contributor.authorYip, Terry Cheuk-Fung-
dc.contributor.authorTse, Yee-Kit-
dc.contributor.authorWong, Grace Lai-Hung-
dc.contributor.authorWong, Vincent Wai-Sun-
dc.contributor.authorChan, Henry Lik-Yuen-
dc.contributor.authorAhn, Sang Hoon-
dc.date.accessioned2021-09-29T01:02:59Z-
dc.date.available2021-09-29T01:02:59Z-
dc.date.created2022-04-06-
dc.date.issued2021-02-
dc.identifier.issn0953-6205-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/184163-
dc.description.abstractBackground & aims: Whether chronic hepatitis B (CHB) patients during immune-tolerant (IT) phase are at low risk of hepatocellular carcinoma (HCC) is still controversial. We performed a multicenter study to determine their long-term prognosis. Methods: Untreated IT group included patients < 40 years of age, with persistently hepatitis B e antigen [HBeAg] positivity, serum HBV-DNA>6 log(10)I U/mL, and ALT level < 40 U/L, using age and HBV-DNA criteria by the American Association for the Study of Liver Diseases (AASLD) guideline. Cumulative HCC risk of untreated IT group (n=194) was compared to HBeAg-positive patients undergoing antiviral therapy according to the practice and reimbursement guidelines (treated HBeAg[+] group, n=454). Patients with history of cirrhosis or HCC at baseline were excluded. Results: During follow-up (median 62.1 months), HCC did not develop in any patient among untreated IT group, whereas the cumulative probability of HCC at 3, 5, and 9 years in the treated HBeAg(+) group was 0.5%, 0.7%, and 1.3%, respectively (p=0.203). Ninety-seven patients among untreated IT group entered immune-active phase, of whom 86 (88.7%) started antiviral treatment. A high normal ALT level (20-39 U/L) was associated with an increased risk of a phase change, compared to ALT < 20 U/L. After censoring at the time of phase change, the cumulative HCC risk was also not significantly different between two groups (p=0.258). Conclusions: No actual HCC risk during untreated IT phase defined by age and HBV-DNA criteria of the AASLD guideline exists, supporting their diagnostic validity from the perspective of long-term prognosis. Further validation studies are required.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier Science-
dc.relation.isPartOfEuropean Journal of Internal Medicine-
dc.relation.isPartOfEUROPEAN JOURNAL OF INTERNAL MEDICINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleNegligible HCC risk during stringently defined untreated immune-tolerant phase of chronic hepatitis B-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorLee, Hye Won-
dc.contributor.googleauthorChon, Young Eun-
dc.contributor.googleauthorKim, Beom Kyung-
dc.contributor.googleauthorYip, Terry Cheuk-Fung-
dc.contributor.googleauthorTse, Yee-Kit-
dc.contributor.googleauthorWong, Grace Lai-Hung-
dc.contributor.googleauthorWong, Vincent Wai-Sun-
dc.contributor.googleauthorChan, Henry Lik-Yuen-
dc.contributor.googleauthorAhn, Sang Hoon-
dc.identifier.doi10.1016/j.ejim.2020.10.022-
dc.relation.journalcodeJ00828-
dc.identifier.eissn1879-0828-
dc.subject.keywordHepatitis B virus-
dc.subject.keywordImmune-tolerant-
dc.subject.keywordAntiviral therapy-
dc.subject.keywordHepatitis B e antigen-
dc.subject.keywordHepatocellular carcinoma-
dc.contributor.alternativeNameKim, Beom Kyung-
dc.contributor.affiliatedAuthorLee, Hye Won-
dc.contributor.affiliatedAuthorKim, Beom Kyung-
dc.contributor.affiliatedAuthorAhn, Sang Hoon-
dc.identifier.scopusid2-s2.0-85097234967-
dc.identifier.wosid000614812200011-
dc.citation.volume84-
dc.citation.startPage68-
dc.citation.endPage73-
dc.identifier.bibliographicCitationEuropean Journal of Internal Medicine, Vol.84 : 68-73, 2021-02-
dc.identifier.rimsid73063-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorHepatitis B virus-
dc.subject.keywordAuthorImmune-tolerant-
dc.subject.keywordAuthorAntiviral therapy-
dc.subject.keywordAuthorHepatitis B e antigen-
dc.subject.keywordAuthorHepatocellular carcinoma-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA-
dc.subject.keywordPlusGUIDELINES-
dc.subject.keywordPlusMANAGEMENT-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.