Efficacy and safety of peginterferon alpha-2a (40 kD) plus ribavirin among patients with chronic hepatitis C and earlier treatment failure to interferon and ribavirin: an open-label study in central and Eastern Europe

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F11%3A00052186" target="_blank" >RIV/00216224:14110/11:00052186 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1097/MEG.0b013e3283458407" target="_blank" >http://dx.doi.org/10.1097/MEG.0b013e3283458407</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1097/MEG.0b013e3283458407" target="_blank" >10.1097/MEG.0b013e3283458407</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Efficacy and safety of peginterferon alpha-2a (40 kD) plus ribavirin among patients with chronic hepatitis C and earlier treatment failure to interferon and ribavirin: an open-label study in central and Eastern Europe

Popis výsledku v původním jazyce

Methods: HCV genotype 1 patients previously treated with conventional interferon with or without ribavirin were assigned to 48 weeks of treatment with peginterferon alfa-2a (40KD) 180 mcg/week plus ribavirin (recommended dose 1000/1200 mg/day) in this open-label trial conducted in Central and Eastern Europe. The primary efficacy endpoint was sustained virological response (SVR, HCV RNA &lt;50 IU/mL) after 24 weeks of untreated follow-up. Early virological response (EVR) was defined as undetectable HCV RNA or minimally 2-log drop at week 12. Results: 154/203 (76%) treatment-experienced genotype 1 patients completed treatment. Overall, 113 patients (56%) achieved an EVR, 107 (53%) had an end-of-treatment response and 63 patients (31%) achieved an SVR (including 38% [40/105] of those with prior breakthrough or relapse and 24% [21/88] of those with prior non-response).

Název v anglickém jazyce

Efficacy and safety of peginterferon alpha-2a (40 kD) plus ribavirin among patients with chronic hepatitis C and earlier treatment failure to interferon and ribavirin: an open-label study in central and Eastern Europe

Popis výsledku anglicky

Methods: HCV genotype 1 patients previously treated with conventional interferon with or without ribavirin were assigned to 48 weeks of treatment with peginterferon alfa-2a (40KD) 180 mcg/week plus ribavirin (recommended dose 1000/1200 mg/day) in this open-label trial conducted in Central and Eastern Europe. The primary efficacy endpoint was sustained virological response (SVR, HCV RNA &lt;50 IU/mL) after 24 weeks of untreated follow-up. Early virological response (EVR) was defined as undetectable HCV RNA or minimally 2-log drop at week 12. Results: 154/203 (76%) treatment-experienced genotype 1 patients completed treatment. Overall, 113 patients (56%) achieved an EVR, 107 (53%) had an end-of-treatment response and 63 patients (31%) achieved an SVR (including 38% [40/105] of those with prior breakthrough or relapse and 24% [21/88] of those with prior non-response).

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FN - Epidemiologie, infekční nemoci a klinická imunologie

OECD FORD obor

—

Projekt

—

Návaznosti

S - Specificky vyzkum na vysokych skolach

Rok uplatnění

2011

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

European Journal of Gastroenterology & Hepatology

ISSN

0954-691X

e-ISSN

—

Svazek periodika

23

Číslo periodika v rámci svazku

5

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

7

Strana od-do

375-381

Kód UT WoS článku

000289506800002

EID výsledku v databázi Scopus

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