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.author | Lee, Hye Won | - |
| dc.contributor.author | Chon, Young Eun | - |
| dc.contributor.author | Kim, Beom Kyung | - |
| dc.contributor.author | Yip, Terry Cheuk-Fung | - |
| dc.contributor.author | Tse, Yee-Kit | - |
| dc.contributor.author | Wong, Grace Lai-Hung | - |
| dc.contributor.author | Wong, Vincent Wai-Sun | - |
| dc.contributor.author | Chan, Henry Lik-Yuen | - |
| dc.contributor.author | Ahn, Sang Hoon | - |
| dc.date.accessioned | 2021-09-29T01:02:59Z | - |
| dc.date.available | 2021-09-29T01:02:59Z | - |
| dc.date.created | 2022-04-06 | - |
| dc.date.issued | 2021-02 | - |
| dc.identifier.issn | 0953-6205 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/184163 | - |
| dc.description.abstract | Background & 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.statementOfResponsibility | restriction | - |
| dc.language | English | - |
| dc.publisher | Elsevier Science | - |
| dc.relation.isPartOf | European Journal of Internal Medicine | - |
| dc.relation.isPartOf | EUROPEAN JOURNAL OF INTERNAL MEDICINE | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.title | Negligible HCC risk during stringently defined untreated immune-tolerant phase of chronic hepatitis B | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
| dc.contributor.googleauthor | Lee, Hye Won | - |
| dc.contributor.googleauthor | Chon, Young Eun | - |
| dc.contributor.googleauthor | Kim, Beom Kyung | - |
| dc.contributor.googleauthor | Yip, Terry Cheuk-Fung | - |
| dc.contributor.googleauthor | Tse, Yee-Kit | - |
| dc.contributor.googleauthor | Wong, Grace Lai-Hung | - |
| dc.contributor.googleauthor | Wong, Vincent Wai-Sun | - |
| dc.contributor.googleauthor | Chan, Henry Lik-Yuen | - |
| dc.contributor.googleauthor | Ahn, Sang Hoon | - |
| dc.identifier.doi | 10.1016/j.ejim.2020.10.022 | - |
| dc.relation.journalcode | J00828 | - |
| dc.identifier.eissn | 1879-0828 | - |
| dc.subject.keyword | Hepatitis B virus | - |
| dc.subject.keyword | Immune-tolerant | - |
| dc.subject.keyword | Antiviral therapy | - |
| dc.subject.keyword | Hepatitis B e antigen | - |
| dc.subject.keyword | Hepatocellular carcinoma | - |
| dc.contributor.alternativeName | Kim, Beom Kyung | - |
| dc.contributor.affiliatedAuthor | Lee, Hye Won | - |
| dc.contributor.affiliatedAuthor | Kim, Beom Kyung | - |
| dc.contributor.affiliatedAuthor | Ahn, Sang Hoon | - |
| dc.identifier.scopusid | 2-s2.0-85097234967 | - |
| dc.identifier.wosid | 000614812200011 | - |
| dc.citation.volume | 84 | - |
| dc.citation.startPage | 68 | - |
| dc.citation.endPage | 73 | - |
| dc.identifier.bibliographicCitation | European Journal of Internal Medicine, Vol.84 : 68-73, 2021-02 | - |
| dc.identifier.rimsid | 73063 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordAuthor | Hepatitis B virus | - |
| dc.subject.keywordAuthor | Immune-tolerant | - |
| dc.subject.keywordAuthor | Antiviral therapy | - |
| dc.subject.keywordAuthor | Hepatitis B e antigen | - |
| dc.subject.keywordAuthor | Hepatocellular carcinoma | - |
| dc.subject.keywordPlus | HEPATOCELLULAR-CARCINOMA | - |
| dc.subject.keywordPlus | GUIDELINES | - |
| dc.subject.keywordPlus | MANAGEMENT | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Medicine, General & Internal | - |
| dc.relation.journalResearchArea | General & Internal Medicine | - |
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