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http://hdl.handle.net/11452/22422
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DC Field | Value | Language |
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dc.contributor.author | Wedemeyer, Heiner | - |
dc.contributor.author | Yurdaydın, Cihan | - |
dc.contributor.author | Dalekos, George N. | - |
dc.contributor.author | Erhardt, Andreas | - |
dc.contributor.author | Çakaloğlu, Yılmaz | - |
dc.contributor.author | Değertekin, Halil | - |
dc.contributor.author | Zeuzern, Stefan | - |
dc.contributor.author | Zachou, Kalliopi | - |
dc.contributor.author | Bozkaya, Hakan | - |
dc.contributor.author | Koch, Armin | - |
dc.contributor.author | Bock, Thomas | - |
dc.contributor.author | Dienes, Hans Peter | - |
dc.contributor.author | Manns, Michael P. | - |
dc.date.accessioned | 2021-10-20T12:18:51Z | - |
dc.date.available | 2021-10-20T12:18:51Z | - |
dc.date.issued | 2011-01-27 | - |
dc.identifier.citation | Wedemeyer, 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.issn | 0028-4793 | - |
dc.identifier.issn | 1533-4406 | - |
dc.identifier.uri | https://doi.org/10.1056/NEJMoa0912696 | - |
dc.identifier.uri | https://www.nejm.org/doi/full/10.1056/NEJMoa0912696 | - |
dc.identifier.uri | http://hdl.handle.net/11452/22422 | - |
dc.description.abstract | BACKGROUND 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.sponsorship | German Ministry for Education and Research, BMBF-Forderkennzeichen | en_US |
dc.description.sponsorship | Hoffmann-La Roche | en_US |
dc.description.sponsorship | Gilead Sciences | en_US |
dc.language.iso | en | en_US |
dc.publisher | Massachusetts Medical Soc | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | D virus infection | en_US |
dc.subject | B virus | en_US |
dc.subject | Combination therapy | en_US |
dc.subject | Vanishing disease | en_US |
dc.subject | Interferon | en_US |
dc.subject | Lamivudine | en_US |
dc.subject | Ribavirin | en_US |
dc.subject | Hbeag | en_US |
dc.subject | Prevalence | en_US |
dc.subject | Dipivoxil | en_US |
dc.title | Peginterferon plus adefovir versus either drug alone for hepatitis delta | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000286592600007 | tr_TR |
dc.identifier.scopus | 2-s2.0-79251490096 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi. | tr_TR |
dc.identifier.startpage | 322 | tr_TR |
dc.identifier.endpage | 331 | tr_TR |
dc.identifier.volume | 364 | tr_TR |
dc.identifier.issue | 4 | tr_TR |
dc.relation.journal | New England Journal of Medicine | en_US |
dc.contributor.buuauthor | Gürel, Selim | - |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.identifier.pubmed | 21268724 | tr_TR |
dc.subject.wos | Medicine, general & internal | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | Pubmed | en_US |
dc.wos.quartile | Q1 | en_US |
dc.contributor.scopusid | 7003706434 | tr_TR |
dc.subject.scopus | Hepatitis Delta Virus; Chronic Hepatitis D; Lonafarnib | en_US |
dc.subject.emtree | Adefovir | en_US |
dc.subject.emtree | Alanine aminotransferase | en_US |
dc.subject.emtree | Hepatitis B surface antigen | en_US |
dc.subject.emtree | Peginterferon alpha2a | en_US |
dc.subject.emtree | Placebo | en_US |
dc.subject.emtree | Virus RNA | en_US |
dc.subject.emtree | Abdominal pain | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Alanine aminotransferase blood level | en_US |
dc.subject.emtree | Anorexia | en_US |
dc.subject.emtree | Antigen detection | en_US |
dc.subject.emtree | Arthralgia | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Clinical article | en_US |
dc.subject.emtree | Coughing | en_US |
dc.subject.emtree | Decompensated liver cirrhosis | en_US |
dc.subject.emtree | Delta agent hepatitis | en_US |
dc.subject.emtree | Dizziness | en_US |
dc.subject.emtree | Drug efficacy | en_US |
dc.subject.emtree | Drug eruption | en_US |
dc.subject.emtree | Drug fever | en_US |
dc.subject.emtree | Drug induced headache | en_US |
dc.subject.emtree | Drug safety | en_US |
dc.subject.emtree | Drug withdrawal | en_US |
dc.subject.emtree | Fatigue | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Flu like syndrome | en_US |
dc.subject.emtree | Follow up | en_US |
dc.subject.emtree | Hair loss | en_US |
dc.subject.emtree | Hemoperitoneum | en_US |
dc.subject.emtree | Histopathology | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | HumantTissue | en_US |
dc.subject.emtree | İnsomnia | en_US |
dc.subject.emtree | Liver cell carcinoma | en_US |
dc.subject.emtree | Malaise | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Myalgia | en_US |
dc.subject.emtree | Nausea | en_US |
dc.subject.emtree | Neutropenia | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Pruritus | en_US |
dc.subject.emtree | Randomized controlled trial | en_US |
dc.subject.emtree | Thrombocytopenia | en_US |
dc.subject.emtree | Treatment outcome | en_US |
dc.subject.emtree | Xerostomia | en_US |
Appears in Collections: | Scopus Web of Science |
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