Publication: High treatment modification rates with lamivudine therapy in HBV-infected patients with low baseline viremia and early virological response: A multicenter study
| dc.contributor.author | GÜNDÜZ, FEYZA | |
| dc.contributor.authors | Gonen, Can; Gunduz, Feyza; Doganay, Levent; Enc, Feruze Y.; Yegin, Ender G.; Ahishali, Emel; Erdem, Emrullah; Sokmen, Mehmet; Tuncer, Ilyas; Ozdogan, Osman | |
| dc.date.accessioned | 2022-03-12T20:26:52Z | |
| dc.date.available | 2022-03-12T20:26:52Z | |
| dc.date.issued | 2015 | |
| dc.description.abstract | ObjectiveLow baseline viremia and an early treatment response predict the best outcomes in hepatitis B virus (HBV)-infected patients treated with nucleoside analogues with low barriers to resistance. The aim of this study was to assess the long-term results and effectiveness of lamivudine in patients with low baseline viremia and early virological treatment response. MethodsIn this multicenter, real-life setting study, 111 antiviral-naive patients with low baseline viremia (HBV DNA <10(7) copies/mL) plus an early virological response (HBV DNA <300 copies/mL at week 24) treated with lamivudine were enrolled. The primary end-point was treatment failure, defined as the re-emergence of detectable viremia or at least a 1 log increase in HBV DNA, resulting in a titer of 300 copies/mL with lamivudine treatment after week 24, which required treatment modification. ResultsAltogether 111 patients, including 78 non-cirrhotic and 33 cirrhotic patients, were included in the study. Treatment failure occurred in 30.8% of the non-cirrhotic patients over a median follow-up period of 32.5 months, and the 1-, 2-, 3-, 4- and 5-year treatment failure rates were 6.5%, 14.0%, 31.4%, 39.6% and 43.1%, respectively. Treatment failure occurred in 28.8% of the whole group. There were no differences between the cirrhotic and non-cirrhotic patients. ConclusionsLamivudine treatment had a high treatment modification rate in patients with low baseline viremia and early virological response over a long-term follow-up in a real-life setting. The pretreatment and on-treatment favorable characteristics found in the studies with telbivudine appeared to be inapplicable to lamivudine. | |
| dc.identifier.doi | 10.1111/1751-2980.12237 | |
| dc.identifier.eissn | 1751-2980 | |
| dc.identifier.issn | 1751-2972 | |
| dc.identifier.pubmed | 25708813 | |
| dc.identifier.uri | https://hdl.handle.net/11424/233575 | |
| dc.identifier.wos | WOS:000355284300006 | |
| dc.language.iso | eng | |
| dc.publisher | WILEY | |
| dc.relation.ispartof | JOURNAL OF DIGESTIVE DISEASES | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | early response | |
| dc.subject | hepatitis B virus | |
| dc.subject | lamivudine | |
| dc.subject | resistance | |
| dc.subject | viral load | |
| dc.subject | CHRONIC HEPATITIS-B | |
| dc.subject | SURFACE-ANTIGEN | |
| dc.subject | VIRUS-DNA | |
| dc.subject | BREAKTHROUGH | |
| dc.title | High treatment modification rates with lamivudine therapy in HBV-infected patients with low baseline viremia and early virological response: A multicenter study | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| local.avesis.id | b8376ba6-77aa-4df0-b1a9-998654bfa7a3 | |
| local.import.package | SS17 | |
| local.indexed.at | WOS | |
| local.indexed.at | SCOPUS | |
| local.indexed.at | PUBMED | |
| local.journal.numberofpages | 7 | |
| oaire.citation.endPage | 292 | |
| oaire.citation.issue | 5 | |
| oaire.citation.startPage | 286 | |
| oaire.citation.title | JOURNAL OF DIGESTIVE DISEASES | |
| oaire.citation.volume | 16 | |
| relation.isAuthorOfPublication | d48af87b-516f-4788-b8af-58d60d712c5e | |
| relation.isAuthorOfPublication.latestForDiscovery | d48af87b-516f-4788-b8af-58d60d712c5e |