Cited 12 times in

Partial virological response to entecavir in treatment-naive patients with chronic hepatitis B.

DC Field Value Language
dc.contributor.author김도영-
dc.contributor.author김승업-
dc.contributor.author김자경-
dc.contributor.author박준용-
dc.contributor.author안상훈-
dc.contributor.author이관식-
dc.contributor.author전영은-
dc.contributor.author전재윤-
dc.contributor.author최은희-
dc.contributor.author한광협-
dc.date.accessioned2014-12-20T17:10:16Z-
dc.date.available2014-12-20T17:10:16Z-
dc.date.issued2011-
dc.identifier.issn1359-6535-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/94091-
dc.description.abstractBACKGROUND: The proposed definition of a partial virological response (PVR) to nucleos(t)ide analogue therapy in the 2009 European Association for the Study of the Liver (EASL) guidelines is based on limited evidence, especially in terms of the cutoff HBV DNA level and the time point at which to judge it. This study assessed optimal PVR criteria for predicting virological response (VR) at week 96 in treatment-naive patients with chronic hepatitis B (CHB) receiving entecavir (ETV). METHODS: A total of 175 patients (126 men, 49 women) who completed 96 weeks of first-line ETV therapy were prospectively recruited. For predicting VR at week 96, the area under the receiver operating characteristic curve (AUC) was used to find the optimal time point and the Youden index was used to calculate the optimal cutoff HBV DNA level. RESULTS: After 96 weeks of ETV therapy, 139 (79.4%) patients achieved VR. The AUC at week 48 was significantly better than that at week 24 for predicting VR at week 96 (P=0.023). The optimal cutoff HBV DNA level at week 48 was 35 IU/ml. Forty-one (23.4%) patients met this PVR criteria of ETV (HBV DNA level >35 IU/ml at week 48). CONCLUSIONS: An HBV DNA level >35 IU/ml at week 48 is the optimal PVR criteria for predicting non-VR at week 96 in treatment-naive patients with CHB who are receiving ETV. This study supports the proposed EASL PVR for ETV based on scientific evidence.-
dc.description.statementOfResponsibilityopen-
dc.format.extent469~477-
dc.relation.isPartOfANTIVIRAL THERAPY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAntiviral Agents/therapeutic use*-
dc.subject.MESHDNA, Viral/blood*-
dc.subject.MESHFemale-
dc.subject.MESHGuanine/analogs & derivatives*-
dc.subject.MESHGuanine/therapeutic use-
dc.subject.MESHHepatitis B virus/drug effects*-
dc.subject.MESHHepatitis B virus/genetics-
dc.subject.MESHHepatitis B virus/physiology-
dc.subject.MESHHepatitis B, Chronic/drug therapy*-
dc.subject.MESHHepatitis B, Chronic/virology-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPredictive Value of Tests-
dc.subject.MESHTime Factors-
dc.subject.MESHTreatment Outcome-
dc.titlePartial virological response to entecavir in treatment-naive patients with chronic hepatitis B.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Biostatistics (의학통계학)-
dc.contributor.googleauthorYoung Eun Chon-
dc.contributor.googleauthorSeung Up Kim-
dc.contributor.googleauthorChun Kyon Lee-
dc.contributor.googleauthorJeong Heo-
dc.contributor.googleauthorJa Kyung Kim-
dc.contributor.googleauthorKi Tae Yoon3, Mong Cho-
dc.contributor.googleauthorKwan Sik Lee-
dc.contributor.googleauthorDong Hwan Kim-
dc.contributor.googleauthorEun Hee Choi-
dc.contributor.googleauthorJun Yong Park-
dc.contributor.googleauthorDo Young Kim-
dc.contributor.googleauthorChae Yoon Chon-
dc.contributor.googleauthorKwang-Hyub Han-
dc.contributor.googleauthorSang Hoon Ahn-
dc.identifier.doi10.3851/IMP1772-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00654-
dc.contributor.localIdA00852-
dc.contributor.localIdA01675-
dc.contributor.localIdA02226-
dc.contributor.localIdA02666-
dc.contributor.localIdA03532-
dc.contributor.localIdA04163-
dc.contributor.localIdA04268-
dc.contributor.localIdA03544-
dc.contributor.localIdA00385-
dc.relation.journalcodeJ00191-
dc.identifier.eissn2040-2058-
dc.identifier.pmid21685534-
dc.identifier.urlhttp://www.intmedpress.com/journals/avt/article.cfm?id=1772&pid=88&sType=AVT-
dc.contributor.alternativeNameKim, Do Young-
dc.contributor.alternativeNameKim, Seung Up-
dc.contributor.alternativeNameKim, Ja Kyung-
dc.contributor.alternativeNamePark, Jun Yong-
dc.contributor.alternativeNameAhn, Sang Hoon-
dc.contributor.alternativeNameLee, Kwan Sik-
dc.contributor.alternativeNameChon, Young Eun-
dc.contributor.alternativeNameChon, Chae Yoon-
dc.contributor.alternativeNameChoi, Eun Hee-
dc.contributor.alternativeNameHan, Kwang Hyup-
dc.contributor.affiliatedAuthorKim, Seung Up-
dc.contributor.affiliatedAuthorKim, Ja Kyung-
dc.contributor.affiliatedAuthorPark, Jun Yong-
dc.contributor.affiliatedAuthorAhn, Sang Hoon-
dc.contributor.affiliatedAuthorLee, Kwan Sik-
dc.contributor.affiliatedAuthorChon, Young Eun-
dc.contributor.affiliatedAuthorChoi, Eun Hee-
dc.contributor.affiliatedAuthorHan, Kwang Hyup-
dc.contributor.affiliatedAuthorChon, Chae Yoon-
dc.contributor.affiliatedAuthorKim, Do Young-
dc.rights.accessRightsnot free-
dc.citation.volume16-
dc.citation.number4-
dc.citation.startPage469-
dc.citation.endPage477-
dc.identifier.bibliographicCitationANTIVIRAL THERAPY, Vol.16(4) : 469-477, 2011-
dc.identifier.rimsid27231-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Biomedical Systems Informatics (의생명시스템정보학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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