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Predictive score for hepatocellular carcinoma after hepatitis B e antigen loss in patients treated with entecavir or tenofovir
DC Field | Value | Language |
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dc.contributor.author | Lim, TS | - |
dc.contributor.author | Lee, HW | - |
dc.contributor.author | Lee, JI | - |
dc.contributor.author | Kim, IH | - |
dc.contributor.author | Lee, CH | - |
dc.contributor.author | Jang, BK | - |
dc.contributor.author | Chung, WJ | - |
dc.contributor.author | Yim, HJ | - |
dc.contributor.author | Suh, SJ | - |
dc.contributor.author | Seo, YS | - |
dc.contributor.author | Lee, HA | - |
dc.contributor.author | Yu, JH | - |
dc.contributor.author | Lee, JW | - |
dc.contributor.author | Kim, SG | - |
dc.contributor.author | Kim, YS | - |
dc.contributor.author | Park, SY | - |
dc.contributor.author | Tak, WY | - |
dc.contributor.author | Kim, SS | - |
dc.contributor.author | Cheong, JY | - |
dc.contributor.author | Jeong, SW | - |
dc.contributor.author | Jang, JY | - |
dc.contributor.author | Rou, WS | - |
dc.contributor.author | Lee, BS | - |
dc.contributor.author | Kim, SU | - |
dc.contributor.author | Korean Transient Elastography Study Group | - |
dc.date.accessioned | 2022-11-23T07:33:02Z | - |
dc.date.available | 2022-11-23T07:33:02Z | - |
dc.date.issued | 2020 | - |
dc.identifier.issn | 1352-0504 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/22890 | - |
dc.description.abstract | The risk of developing hepatocellular carcinoma (HCC) after hepatitis B e antigen seroclearance (ESC) remains unclear. We established and validated a new risk prediction model for HCC development after ESC in patients with chronic hepatitis B (CHB) receiving antiviral therapy (AVT). Between 2006 and 2016, 769 patients (training cohort) and 1,061 patients (validation cohort) with CHB who experienced ESC during AVT using entecavir (ETV) or tenofovir disoproxil fumarate (TDF) were recruited. In the multivariate analysis, male sex (hazard ratio [HR] = 2.092; 95% confidence interval [CI] = 1.152-3.800), cirrhosis (HR = 5.141; 95% CI = 2.367-11.167) and fibrosis-4 index (FIB-4) of >3.25 (HR = 2.070; 95% CI = 1.184-3.620) were the independent risk factors for HCC development (all P < .05). Accordingly, a novel HCC-ESCAVT model was developed (1x[sex: male = 1, female = 0] + 3x(cirrhosis = 1, noncirrhosis = 0) + 1x(FIB-4: >3.25 = 1, 3.25 as constituent variables. | - |
dc.language.iso | en | - |
dc.subject.MESH | Antiviral Agents | - |
dc.subject.MESH | Carcinoma, Hepatocellular | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Guanine | - |
dc.subject.MESH | Hepatitis B e Antigens | - |
dc.subject.MESH | Hepatitis B, Chronic | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Liver Neoplasms | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Tenofovir | - |
dc.title | Predictive score for hepatocellular carcinoma after hepatitis B e antigen loss in patients treated with entecavir or tenofovir | - |
dc.type | Article | - |
dc.identifier.pmid | 32383246 | - |
dc.subject.keyword | hepatitis B | - |
dc.subject.keyword | hepatitis B e antigen | - |
dc.subject.keyword | hepatocellular carcinoma | - |
dc.subject.keyword | risk prediction | - |
dc.contributor.affiliatedAuthor | Kim, SS | - |
dc.contributor.affiliatedAuthor | Cheong, JY | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1111/jvh.13316 | - |
dc.citation.title | Journal of viral hepatitis | - |
dc.citation.volume | 27 | - |
dc.citation.number | 10 | - |
dc.citation.date | 2020 | - |
dc.citation.startPage | 1052 | - |
dc.citation.endPage | 1060 | - |
dc.identifier.bibliographicCitation | Journal of viral hepatitis, 27(10). : 1052-1060, 2020 | - |
dc.embargo.liftdate | 9999-12-31 | - |
dc.embargo.terms | 9999-12-31 | - |
dc.identifier.eissn | 1365-2893 | - |
dc.relation.journalid | J013520504 | - |
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