Combination therapy of interferon-alpha [PDferon and B®] ribavirin for chronic hepatitis C
Hepatitis Monthly. 2004; 4 (6): 13-16
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EMRO
Introduction: the addition of ribavirin [RIBA] to the standard treatment with interferon [IFN] alpha led to an improvement in sustained virologic response [SVR] from less than 20% with IFN monotherapy to 40-45% in combination therapy. The aim of this study is to assess the therapeutic efficacy and safety of IFN alpha [PDferon B®] in combination with RIBA on Iranian patients with chronic hepatitis C [CHC]
Methods: 48 naive patients aged 18 years or more with CHC were enrolled and treated with 3 mega units [MU] IFN alpha-2b three times a week plus 800-1000 mg RIBA per day for 48 weeks. Follow-up after therapy was 6 months. The efficacy was evident at the end of treatment and at the end of follow-up in terms of sustained normalization of alanine aminotransferase and sustained serum HCV-RNA loss
Results: the rate of sustained biochemical and virologic response were 68.3% and 78%, respectively. Virologic response was 80.9% and 86.4% at weeks 12 and 48 as well. Any patient didn't have serious complication
Conclusion: although we had no control group who used standard IFN, our preliminary finding showed acceptable and promising response rate of PDferon. On the other hand, it seems that adverse events with PDferon are as like as other standard IFNs
Methods: 48 naive patients aged 18 years or more with CHC were enrolled and treated with 3 mega units [MU] IFN alpha-2b three times a week plus 800-1000 mg RIBA per day for 48 weeks. Follow-up after therapy was 6 months. The efficacy was evident at the end of treatment and at the end of follow-up in terms of sustained normalization of alanine aminotransferase and sustained serum HCV-RNA loss
Results: the rate of sustained biochemical and virologic response were 68.3% and 78%, respectively. Virologic response was 80.9% and 86.4% at weeks 12 and 48 as well. Any patient didn't have serious complication
Conclusion: although we had no control group who used standard IFN, our preliminary finding showed acceptable and promising response rate of PDferon. On the other hand, it seems that adverse events with PDferon are as like as other standard IFNs
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Índice:
IMEMR
Idioma:
En
Revista:
Hepat. Monthly
Ano de publicação:
2004