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dc.contributor.author Hunyady, Béla
dc.contributor.author Abonyi, Margit
dc.contributor.author Csefko K
dc.contributor.author Gervain J
dc.contributor.author Haragh A
dc.contributor.author Horvath G
dc.contributor.author Jancsik V
dc.contributor.author Makkai E
dc.contributor.author Muller Z
dc.contributor.author Ribiczey P
dc.contributor.author Sipos B
dc.contributor.author Szabo O
dc.contributor.author Szalay, Ferenc
dc.contributor.author Szentgyorgyi L
dc.contributor.author Tornai I
dc.contributor.author Ujhelyi E
dc.contributor.author Varga M
dc.contributor.author Weisz G
dc.contributor.author Makara M
dc.date.accessioned 2018-09-24T09:29:38Z
dc.date.available 2018-09-24T09:29:38Z
dc.date.issued 2016
dc.identifier 84983339896
dc.identifier.citation pagination=1366-1374; journalVolume=157; journalIssueNumber=34; journalTitle=ORVOSI HETILAP;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/5867
dc.identifier.uri doi:10.1556/650.2016.30538
dc.description.abstract INTRODUCTION: During 2011 and 2013, 155 Hungarian hepatitis C genotype 1 infected patients, mostly with advanced liver fibrosis, who did not respond to prior peginterferon + ribavirin dual therapy, started boceprevir based triple therapy in an early access program. AIM AND METHOD: Efficacy and safety of the therapy was retrospectively assessed based on sustained virologic responses, as well as on frequency and type of serious adverse events and of those leading to therapy discontinuation. RESULTS: In an intent-to-treat analysis 39.4% patients (61/155) reached sustained virologic response. Amongst pervious relapsers, partial responders and null-responders 59.5%, 41.4 % and 22.9% (p<0.05 compared to the other two categories) reached sustained virologic response, respectively, while amongst non-cirrhotics and cirrhotics 52.5% and 31.3% (p<0.05 compared to the non-cirrhotics) achieved sutained virologic response, respectively. Six out of the 33 most difficult to cure patients (previous null responder and cirrhotic) have reached sustained virologic response (18.2%). Frequency of early discontinuations due to insufficient virologic response was 31.1%, while due to adverse event 10.3%. Reported frequency of serious adverse event was 9.8%. These events represented anemia, diarrhoea, depression, agranulocytosis, elevated aminotransferases, generalized dermatitis and severe gingivitis with loss of teeth, prolonged QT interval on ECG, generalized oedema and severe dyspnoea, uroinfection, exacerbation of Crohn's disease, Campylobacter pylori infection and unacceptable weakness and fatigue. Eight patients received transfusion, 4 patients erythropoietin and 1 granulocyte colony stimulating factor during therapy. No death has been reported. CONCLUSIONS: With boceprevir based triple therapy, one of the bests available in 2011-2013 in Hungary, a relevant proportion of hepatitis C infected patients with advanced liver fibrosis achieved sustained viral response. In this cohort, side-effects resembled those reported in registration studies, and resulted in therapy discontinuation with consequent treatment failure in a relevant number of patients. Efficacy and tolerability of boceprevir-based triple therapy are suboptimal, particularly in the most difficult to cure patient population. Orv. Hetil., 2016, 157(34), 1366-1374.
dc.relation.ispartof urn:issn:0030-6002
dc.title Bocepreviralapú hármas kezelés hatékonyságának és biztonságosságának retrospektív elemzése előrehaladott fibrosisstádiumú, hepatitis C-vírus 1-es genotípussal fertőzött, korábban sikertelenül kezelt magyar betegeknél
dc.type Journal Article
dc.date.updated 2018-07-17T10:03:43Z
dc.language.rfc3066 hu
dc.identifier.mtmt 3105007
dc.identifier.wos 000382796700006
dc.identifier.pubmed 27546804
dc.contributor.department SE/AOK/K/I. Sz. Belgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem
dc.mtmt.swordnote


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