Based on the first decade of research on alpha interferon and improving hepatic histology. The discovery and characterization of the hepatitis C virus (HCV) led to reanalysis of in viral hepatitis, one can conclude that up to 40% of patients with compensated chronic hepatitis C and elevated alanine
Optimal therapy of hepatitis C
β Scribed by Adrian M. Di Bisceglie; Jay H. Hoofnagle
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 745 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
β¦ Synopsis
The highest response rates to antiviral therapy for the treatment of chronic hepatitis C have been achieved using the combination of peginterferon and ribavirin. Recently completed controlled trials have reported rates of sustained virological response (SVR) between 50% and 60% in patients treated with higher doses of peginterferon and ribavirin, which was 5% to 10% higher with standard doses of interferon alfa and ribavirin. The major determinant of outcome of therapy is hepatitis C virus (HCV) genotype. With the combination of peginterferon and ribavirin, patients with genotype I achieve response rates of 40% to 45%, compared with rates approaching 80% with genotypes 2 or 3. Importantly, patients with HCV genotype I achieve higher rates of response with 48 weeks than with 24 weeks of therapy, whereas patients with genotypes 2 and 3 are adequately treated with a 24-week course. Furthermore, patients with genotypes 2 and 3 require only 800 mg of ribavirin daily to achieve optimal response rates, whereas 1,000 to 1,200 mg daily is needed for patients with genotype I . Future studies should focus on optimizing the dose of peginterferon and ribavirin by patient characteristics, particularly on resolving the issue of weight-based dosing. For patients with good prognostic factors, a lower dose and shorter course of peginterferon may be adequate for full effect. Importantly, research is needed to show how treatment regimens can best be applied to other patient groups with hepatitis C, such as patients with acute hepatitis, human immunodeficiency virus coinfection, renal disease, solid-organ transplant, neuropyschiatric disease, autoimmunity, and alcohol or substance abuse. (HEPATOLOGY 2002;36:S121-S127.) 0 nly recently have effective therapies become available for the treatment of hepatitis C. The beneficial effects of interferon alfa in hepatitis C were first reported in 1986, and subsequent studies led to its approval for use in hepatitis C by the U.S. Food and Drug Administration in 1990. At the time of the first Consensus Development Conference in 1997, the Consensus panel recommended a course of interferon alfa at a ~~~~~ Abbreviations: SVR, sustained virological response: HCK hepatitis C virus.
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