Peginterferon alfa-2b plus ribavirin for treatment of chronic hepatitis C in previously untreated patients infected with HCV genotypes 2 or 3*1, *2

التفاصيل البيبلوغرافية
العنوان: Peginterferon alfa-2b plus ribavirin for treatment of chronic hepatitis C in previously untreated patients infected with HCV genotypes 2 or 3*1, *2
المؤلفون: Janice K. Albrecht, Patrick Marcellin, Joann Harvey, José María Sánchez-Tapias, Clifford A. Brass, Tobias Goeser, Christoph Sarrazin, Rolf Hultcrantz, Stefan Zeuzem, Marc Bourlière
المصدر: Journal of Hepatology. 40:993-999
بيانات النشر: Elsevier BV, 2004.
سنة النشر: 2004
مصطلحات موضوعية: medicine.medical_specialty, Hepacivirus, Hepatitis C virus, Population, medicine.disease_cause, Gastroenterology, chemistry.chemical_compound, Pegylated interferon, Internal medicine, medicine, education, education.field_of_study, Hepatology, biology, business.industry, Ribavirin, virus diseases, Hepatitis C, medicine.disease, biology.organism_classification, digestive system diseases, Discontinuation, chemistry, Immunology, Peginterferon alfa-2b, business, medicine.drug
الوصف: Background/Aims Treatment duration in patients with chronic hepatitis C in the era of standard interferon-α plus ribavirin was tailored according to hepatitis C virus (HCV) genotype: patients infected with HCV-1 were treated for 48 weeks, patients infected with HCV-2/3 for 24 weeks. The aim of the present study was to investigate this schedule for HCV-2/3 infected patients in the era of pegylated interferon-α plus ribavirin. Methods Patients chronically infected with HCV-2 ( n =42) or HCV-3 ( n =182) were treated with peginterferon alfa-2b 1.5 μg/kg subcutaneously once weekly plus ribavirin 800–1400 mg/day based on body weight for 24 weeks. Results The end of treatment (EOT) and sustained virologic response (SVR) was higher in patients infected with HCV-2 (100 and 93%, respectively) than in patients infected with HCV-3 (93 and 79%, respectively). Baseline viremia ( P =0.020), treatment duration >16 weeks ( P P =0.015) were significant independent predictors of SVR. Adverse events resulted in discontinuation in 5% and dose reduction in 22% of patients. Conclusions Treatment for 24 weeks with peginterferon alfa-2b and ribavirin is sufficient in HCV 2 or 3 infected patients. The lower SVR in patients infected with HCV-3 compared with HCV-2 infected patients may be related to higher levels of steatosis in this population.
تدمد: 0168-8278
DOI: 10.1016/j.jhep.2004.02.007
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::73f741a43c9aba230b6685a440aa8c8d
https://doi.org/10.1016/j.jhep.2004.02.007
Rights: CLOSED
رقم الانضمام: edsair.doi...........73f741a43c9aba230b6685a440aa8c8d
قاعدة البيانات: OpenAIRE
الوصف
تدمد:01688278
DOI:10.1016/j.jhep.2004.02.007