Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/6730
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dc.contributor.authorSimonović Babić J.en
dc.contributor.authorBojović K.en
dc.contributor.authorFabri M.en
dc.contributor.authorKostić, Vladimiren
dc.contributor.authorJovanović, Markoen
dc.contributor.authorMijailović Ž.en
dc.contributor.authorSvorcan P.en
dc.contributor.authorJanković G.en
dc.date.accessioned2019-09-30T08:57:04Z-
dc.date.available2019-09-30T08:57:04Z-
dc.date.issued2015-01-01en
dc.identifier.issn03708179en
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/6730-
dc.description.abstract© 2015 Serbia Medical Society. All rightsreserved. Introduction The triple therapy which consists of one of the protease inhibitor plus pegylated interferon and ribavirin (P/R) is the standard of care for the treatment of chronic hepatitis C virus (HCV) genotype 1(G1) infection both in treatment-naive and experienced patients. Objective The aim of this study was to analyze the efficacy and tolerability of this regime in hospital practice in Serbia. Methods From July 2012 to October 2012, 20 previously treated patients with advanced fibrosis and HCV G1 infection were included in the triple antiviral regimen in six referral centers in Serbia. All patients were treated with response guide therapy (RGT) regime according to the boceprevir treatment protocol. During the 4-week lead-in period all patients received peginterferon plus ribavirin. After the lead-in period boceprevir was added in the dosage of 800 mg three times a day orally. The subsequent treatment varied according to virologic response and fibrosis. During the therapy HCV RNA level was measured at week 4, 8, 12, 24 of the treatment for the assessment of virologic response profile. All patients who completed therapy were assessed at the end of the treatment and at the end of an additional 24-week treatment-free period for a sustained virologic response (SVR). Results The total of 20 patients with advanced fibrosis was treated. Among patients with an undetectable HCV RNA level at week 8 the rate of SVR was 100%. No patient with decrease in the HCV RNA level <1 log 10 IU/ml at treatment week 4 achieved SVR. The overall rate of SVR was 55%. The safety profile of the treatment regimen was good. Anemia was reported in 25% of patients. There was no life-threatening treatment adverse event. Conclusion Boceprevir in combination with P/R achieved fairly good SVR rates in patients that were "most difficult to treat" who failed on dual therapy and was effective among patients with cirrhosis.en
dc.relation.ispartofSrpski Arhiv za Celokupno Lekarstvoen
dc.titleBoceprevir in genotype 1 chronic hepatitis C: First experiences in Serbiaen
dc.typeJournal/Magazine Articleen
dc.identifier.doi10.2298/SARH1502035Sen
dc.identifier.pmid143en
dc.identifier.scopus2-s2.0-84924414905en
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84924414905en
dc.relation.lastpage41en
dc.relation.firstpage35en
dc.relation.issue1-2en
dc.relation.volume143en
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptPrirodno-matematički fakultet, Departman za matematiku i informatiku-
crisitem.author.parentorgPrirodno-matematički fakultet-
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