Peginterferon plus adefovir versus either drug alone for hepatitis delta

dc.contributor.authorWedemeyer, Heiner
dc.contributor.authorYurdaydın, Cihan
dc.contributor.authorDalekos, George N.
dc.contributor.authorErhardt, Andreas
dc.contributor.authorÇakaloğlu, Yılmaz
dc.contributor.authorDeğertekin, Halil
dc.contributor.authorZeuzern, Stefan
dc.contributor.authorZachou, Kalliopi
dc.contributor.authorBozkaya, Hakan
dc.contributor.authorKoch, Armin
dc.contributor.authorBock, Thomas
dc.contributor.authorDienes, Hans Peter
dc.contributor.authorManns, Michael P.
dc.contributor.buuauthorGürel, Selim
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi.tr_TR
dc.contributor.scopusid7003706434tr_TR
dc.date.accessioned2021-10-20T12:18:51Z
dc.date.available2021-10-20T12:18:51Z
dc.date.issued2011-01-27
dc.description.abstractBACKGROUND Chronic infection with hepatitis B virus and hepatitis delta virus (HDV) results in the most severe form of viral hepatitis. There is no currently approved treatment. We investigated the safety and efficacy of 48 weeks of treatment with peginterferon alfa-2a plus adefovir dipivoxil, peginterferon alfa-2a alone, and adefovir dipivoxil alone. METHODS We conducted a randomized trial in which 31 patients with HDV infection received treatment with 180 mu g of peginterferon alfa-2a weekly plus 10 mg of adefovir daily, 29 received 180 mu g of peginterferon alfa-2a weekly plus placebo, and 30 received 10 mg of adefovir alone weekly for 48 weeks. Follow-up was conducted for an additional 24 weeks. Efficacy end points included clearance of HDV RNA, normalization of alanine aminotransferase levels, and a decline in levels of hepatitis B surface antigen (HBsAg). RESULTS The primary end point - normalization of alanine aminotransferase levels and clearance of HDV RNA at week 48 - was achieved in two patients in the group receiving peginterferon alfa-2a plus adefovir and two patients in the group receiving peginterferon alfa-2a plus placebo but in none of the patients in the group receiving adefovir alone. At week 48, the test for HDV RNA was negative in 23% of patients in the first group, 24% of patients in the second, and none of those in the third (P=0.006 for the comparison of the first and third groups; P=0.004 for the comparison of the second and third). The efficacy of peginterferon alfa-2a was sustained for 24 weeks after treatment, with 28% of the patients receiving peginterferon alfa-2a plus adefovir or peginterferon alfa-2a alone having negative results on HDV-RNA tests; none of the patients receiving adefovir alone had negative results. A decline in HBsAg levels of more than 1 log(10) IU per milliliter from baseline to week 48 was observed in 10 patients in the first group, 2 in the second, and none in the third (P<0.001 for the comparison of the first and third groups and P=0.01 for the comparison of the first and second). CONCLUSIONS Treatment with peginterferon alfa-2a for 48 weeks, with or without adefovir, resulted in sustained HDV RNA clearance in about one quarter of patients with HDV infection.tr_TR
dc.description.sponsorshipGerman Ministry for Education and Research, BMBF-Forderkennzeichenen_US
dc.description.sponsorshipHoffmann-La Rocheen_US
dc.description.sponsorshipGilead Sciencesen_US
dc.identifier.citationWedemeyer, H. vd. (2011). "Peginterferon plus adefovir versus either drug alone for hepatitis delta". New England Journal of Medicine, 364(4), 322-331.en_US
dc.identifier.endpage331tr_TR
dc.identifier.issn0028-4793
dc.identifier.issn1533-4406
dc.identifier.issue4tr_TR
dc.identifier.pubmed21268724tr_TR
dc.identifier.scopus2-s2.0-79251490096tr_TR
dc.identifier.startpage322tr_TR
dc.identifier.urihttps://doi.org/10.1056/NEJMoa0912696
dc.identifier.urihttps://www.nejm.org/doi/full/10.1056/NEJMoa0912696
dc.identifier.urihttp://hdl.handle.net/11452/22422
dc.identifier.volume364tr_TR
dc.identifier.wos000286592600007tr_TR
dc.indexed.pubmedPubmeden_US
dc.indexed.scopusScopusen_US
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherMassachusetts Medical Socen_US
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.relation.collaborationSanayitr_TR
dc.relation.journalNew England Journal of Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectD virus infectionen_US
dc.subjectB virusen_US
dc.subjectCombination therapyen_US
dc.subjectVanishing diseaseen_US
dc.subjectInterferonen_US
dc.subjectLamivudineen_US
dc.subjectRibavirinen_US
dc.subjectHbeagen_US
dc.subjectPrevalenceen_US
dc.subjectDipivoxilen_US
dc.subject.emtreeAdefoviren_US
dc.subject.emtreeAlanine aminotransferaseen_US
dc.subject.emtreeHepatitis B surface antigenen_US
dc.subject.emtreePeginterferon alpha2aen_US
dc.subject.emtreePlaceboen_US
dc.subject.emtreeVirus RNAen_US
dc.subject.emtreeAbdominal painen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAlanine aminotransferase blood levelen_US
dc.subject.emtreeAnorexiaen_US
dc.subject.emtreeAntigen detectionen_US
dc.subject.emtreeArthralgiaen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeClinical articleen_US
dc.subject.emtreeCoughingen_US
dc.subject.emtreeDecompensated liver cirrhosisen_US
dc.subject.emtreeDelta agent hepatitisen_US
dc.subject.emtreeDizzinessen_US
dc.subject.emtreeDrug efficacyen_US
dc.subject.emtreeDrug eruptionen_US
dc.subject.emtreeDrug feveren_US
dc.subject.emtreeDrug induced headacheen_US
dc.subject.emtreeDrug safetyen_US
dc.subject.emtreeDrug withdrawalen_US
dc.subject.emtreeFatigueen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFlu like syndromeen_US
dc.subject.emtreeFollow upen_US
dc.subject.emtreeHair lossen_US
dc.subject.emtreeHemoperitoneumen_US
dc.subject.emtreeHistopathologyen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHumantTissueen_US
dc.subject.emtreeİnsomniaen_US
dc.subject.emtreeLiver cell carcinomaen_US
dc.subject.emtreeMalaiseen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMyalgiaen_US
dc.subject.emtreeNauseaen_US
dc.subject.emtreeNeutropeniaen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreePruritusen_US
dc.subject.emtreeRandomized controlled trialen_US
dc.subject.emtreeThrombocytopeniaen_US
dc.subject.emtreeTreatment outcomeen_US
dc.subject.emtreeXerostomiaen_US
dc.subject.scopusHepatitis Delta Virus; Chronic Hepatitis D; Lonafarniben_US
dc.subject.wosMedicine, general & internalen_US
dc.titlePeginterferon plus adefovir versus either drug alone for hepatitis deltaen_US
dc.typeArticle
dc.wos.quartileQ1en_US

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