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dc.creatorKeskin O., Wedemeyer H., Tüzün A., Zachou K., Deda X., Dalekos G.N., Heidrich B., Pehlivan S., Zeuzem S., Yalçin K., Gürel S., Tabak F., Idilman R., Bozkaya H., Manns M., Yurdaydin C.en
dc.date.accessioned2023-01-31T08:43:16Z
dc.date.available2023-01-31T08:43:16Z
dc.date.issued2015
dc.identifier10.1016/j.cgh.2015.05.029
dc.identifier.issn15423565
dc.identifier.urihttp://hdl.handle.net/11615/74871
dc.description.abstractBackground & Aims: Interferon is the only effective treatment for chronic hepatitis D virus (HDV) infection. No rules have been set for stopping treatment based on viral kinetics. We analyzed data from an international study of hepatitis D treatment to identify factors associated with outcomes of pegylated interferon treatment, with and without adefovir. Methods: We analyzed data from the Hep-Net-International Delta Hepatitis Intervention Trial on 50 patients with compensated liver disease who tested positive for anti-HDV and HDV RNA. Subjects received pegylated interferon α 2a, with adefovir or placebo, or only adefovir, for 48 weeks. Twenty-four weeks after treatment ended, 41 patients were evaluated for levels of HDV RNA and DNA, liver enzymes, and hepatitis B surface antigen (HBsAg); liver biopsy specimens were analyzed for fibrosis. Response to therapy was defined as end-of-treatment response or post-treatment week 24 virologic response. In both cases virologic response was associated with undetectable HDV RNA levels. Patients with less than a 1 log decrease in HDV RNA at the end of treatment were considered null responders. Results: Based on univariate and multivariate analysis, the level of HDV RNA at week 24 of treatment was associated more strongly with response to therapy than other factors analyzed. The level of HBsAg at week 24 of treatment was associated with a response to therapy only in univariate analysis. Lack of HDV RNA at week 24 of treatment, or end of treatment, identified responders with positive predicted values of 71% and 100%, respectively. At 24 weeks after treatment, a decrease in HDV RNA level of less than 1 log, combined with no decrease in HBsAg level, identified null responders with a positive predictive value of 83%. A decrease in HDV RNA level of more than 2 log at week 24 of treatment identified null responders with a negative predictive value of 95%. Conclusions: Based on an analysis of data from a large clinical trial, the level of HDV RNA at week 24 of treatment with pegylated interferon, with or without adefovir for 48 weeks, can identify patients who will test negative for HDV RNA 24 weeks after the end of treatment. This information can be used to help physicians manage patients receiving therapy for chronic hepatitis D. © 2015.en
dc.language.isoenen
dc.sourceClinical Gastroenterology and Hepatologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84947244327&doi=10.1016%2fj.cgh.2015.05.029&partnerID=40&md5=e9aeced2f3a45e6089f25d86de934891
dc.subjectadefoviren
dc.subjectadefovir dipivoxilen
dc.subjecthepatitis B surface antigenen
dc.subjectliver enzymeen
dc.subjectpeginterferon alpha2aen
dc.subjectplaceboen
dc.subjectvirus DNAen
dc.subjectvirus RNAen
dc.subjectadenineen
dc.subjectalpha interferonen
dc.subjectaminotransferaseen
dc.subjectantivirus agenten
dc.subjecthepatitis B surface antigenen
dc.subjectmacrogol derivativeen
dc.subjectpeginterferon alpha2aen
dc.subjectphosphonic acid derivativeen
dc.subjectplaceboen
dc.subjectrecombinant proteinen
dc.subjectvirus DNAen
dc.subjectvirus RNAen
dc.subjectadulten
dc.subjectArticleen
dc.subjectclinical articleen
dc.subjectcombination chemotherapyen
dc.subjectcontrolled clinical trialen
dc.subjectcontrolled studyen
dc.subjectdelta agent hepatitisen
dc.subjectdisease associationen
dc.subjectdrug efficacyen
dc.subjectfemaleen
dc.subjectfollow upen
dc.subjecthumanen
dc.subjecthuman tissueen
dc.subjectliver biopsyen
dc.subjectliver fibrosisen
dc.subjectmaleen
dc.subjectmonotherapyen
dc.subjectnonhumanen
dc.subjectoutcome assessmenten
dc.subjectpredictive valueen
dc.subjecttreatment durationen
dc.subjecttreatment responseen
dc.subjectanalogs and derivativesen
dc.subjectbiopsyen
dc.subjectblooden
dc.subjectclinical trialen
dc.subjectgeneticsen
dc.subjectHepatitis D, Chronicen
dc.subjectHepatitis delta virusen
dc.subjectisolation and purificationen
dc.subjectliver cirrhosisen
dc.subjectmiddle ageden
dc.subjectpathologyen
dc.subjecttreatment outcomeen
dc.subjectvirus loaden
dc.subjectAdenineen
dc.subjectAdulten
dc.subjectAntiviral Agentsen
dc.subjectBiopsyen
dc.subjectDNA, Viralen
dc.subjectFemaleen
dc.subjectHepatitis B Surface Antigensen
dc.subjectHepatitis D, Chronicen
dc.subjectHepatitis Delta Virusen
dc.subjectHumansen
dc.subjectInterferon-alphaen
dc.subjectLiver Cirrhosisen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectOrganophosphonatesen
dc.subjectPlacebosen
dc.subjectPolyethylene Glycolsen
dc.subjectRecombinant Proteinsen
dc.subjectRNA, Viralen
dc.subjectTransaminasesen
dc.subjectTreatment Outcomeen
dc.subjectViral Loaden
dc.subjectW.B. Saundersen
dc.titleAssociation Between Level of Hepatitis D Virus RNA at Week 24 of Pegylated Interferon Therapy and Outcomeen
dc.typejournalArticleen


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