34 108

Cited 51 times in

Risk score model for the development of hepatocellular carcinoma in treatment-naïve patients receiving oral antiviral treatment for chronic hepatitis B

DC Field Value Language
dc.contributor.author이정일-
dc.date.accessioned2023-08-09T02:35:42Z-
dc.date.available2023-08-09T02:35:42Z-
dc.date.issued2017-06-
dc.identifier.issn2287-2728-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/195660-
dc.description.abstractBackground/aims: This study aimed to develop and validate a risk prediction model for the development of hepatocellular carcinoma (HCC) in treatment-naïve patients receiving oral antiviral treatment for chronic hepatitis B (CHB). Methods: We investigated 2,061 Korean treatment-naïve patients with CHB treated with entecavir as an initial therapy. A risk score model for HCC development was developed based on multivariable Cox regression model in a single center (n=990) and was validated using the time-dependent area under the receiver operating characteristic curve (AUROC) in three other centers (n=1,071). The difference of HCC development among risk groups (low, intermediate, and high) categorized by risk score was also investigated. Results: The cumulative incidence rates of HCC at 5 years were 11.2% and 8.9% in the testing and validation cohorts, respectively. HCC-Risk Estimating Score in CHB patients Under Entecavir (HCC-RESCUE) is formulated as (age+15×gender [female=0 / male=1]+23×cirrhosis [absence=0 / presence=1]). The AUROCs at 1 year, 3 years, and 5 years were 0.82, 0.81, and 0.81, respectively, in the validation cohort. A significant difference of HCC development in each risk group was determined by the 5-year HCC risk score in the validation cohort (low risk group, 2.1%; intermediate risk group, 9.3%; high risk group, 41.2%, p<0.001). Conclusions: The study presents a new risk score model with a good ability to predict HCC development and determine high risk patients for HCC development consisting of readily available clinical factors in treatment-naïve CHB patients receiving entecavir.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherKorean Association for the Study of the Liver-
dc.relation.isPartOfCLINICAL AND MOLECULAR HEPATOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdministration, Oral-
dc.subject.MESHAdult-
dc.subject.MESHAntiviral Agents / therapeutic use*-
dc.subject.MESHArea Under Curve-
dc.subject.MESHCarcinoma, Hepatocellular / diagnosis*-
dc.subject.MESHCarcinoma, Hepatocellular / epidemiology-
dc.subject.MESHCarcinoma, Hepatocellular / etiology-
dc.subject.MESHDNA, Viral / blood-
dc.subject.MESHDNA, Viral / genetics-
dc.subject.MESHDNA, Viral / metabolism-
dc.subject.MESHFemale-
dc.subject.MESHGuanine / analogs & derivatives*-
dc.subject.MESHGuanine / therapeutic use-
dc.subject.MESHHepatitis B e Antigens / blood-
dc.subject.MESHHepatitis B virus / isolation & purification-
dc.subject.MESHHepatitis B, Chronic / complications-
dc.subject.MESHHepatitis B, Chronic / drug therapy*-
dc.subject.MESHHepatitis B, Chronic / virology-
dc.subject.MESHHumans-
dc.subject.MESHIncidence-
dc.subject.MESHLiver Neoplasms / diagnosis*-
dc.subject.MESHLiver Neoplasms / epidemiology-
dc.subject.MESHLiver Neoplasms / etiology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHProportional Hazards Models-
dc.subject.MESHROC Curve-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHRisk Factors-
dc.titleRisk score model for the development of hepatocellular carcinoma in treatment-naïve patients receiving oral antiviral treatment for chronic hepatitis B-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorWon Sohn-
dc.contributor.googleauthorJu-Yeon Cho-
dc.contributor.googleauthorJi Hoon Kim-
dc.contributor.googleauthorJung Il Lee-
dc.contributor.googleauthorHyung Joon Kim-
dc.contributor.googleauthorMin-Ah Woo-
dc.contributor.googleauthorSin-Ho Jung-
dc.contributor.googleauthorYong-Han Paik-
dc.identifier.doi10.3350/cmh.2016.0086-
dc.contributor.localIdA03122-
dc.relation.journalcodeJ00557-
dc.identifier.eissn2287-285X-
dc.identifier.pmid28506056-
dc.subject.keywordAntiviral drugs-
dc.subject.keywordAssessment, Risk-
dc.subject.keywordChronic hepatitis B-
dc.subject.keywordHepatocellular carcinoma-
dc.contributor.alternativeNameLee, Jung Il-
dc.contributor.affiliatedAuthor이정일-
dc.citation.volume23-
dc.citation.number2-
dc.citation.startPage170-
dc.citation.endPage178-
dc.identifier.bibliographicCitationCLINICAL AND MOLECULAR HEPATOLOGY, Vol.23(2) : 170-178, 2017-06-
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.