HIVandHepatitis.com Highlights from the
56th Annual AASLD Conference

 November 11 - 15, 2005 San Francisco, California

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Treatment of Acute HCV Infection with Pegylated Interferon

By Marina Nunez, MD

In a study conducted in Seattle, subjects with a positive anti-HCV test having tested negative with the past 12 months were treated with 6 months of pegylated interferon (pegIFN) monotherapy to determine the efficacy of this drug in acute HCV infection. The brand of pegIFN used in the study is not specified.

Patients were recruited from a longitudinal study of HIV and HCV seronegative injection drug users (IDU) who are followed for 1 year to measure the incidence of HIV and HCV infections. Thirty IDU seroconverters were randomized to receive no treatment or to receive pegIFN for 6 months. The lag time between the diagnosis and the initiation of therapy is not clear

Only 9 patients started pegIFN treatment (6 HCV-1 and 3 HCV-2/3), and 12 subjects remained untreated as controls (8 HCV-1 and 4 HCV-2/3). The treatment was concluded by 7 individuals, 6 of whom achieved sustained virological response (87%). Out of the 12 controls, only 2 cleared the virus (17%) spontaneously.

During the study period, two serious adverse events occurred, both in the treatment arm (1 suicidal ideation and 1 death due to alcohol/heroin overdose). In addition, 3 of 21 (14%) subjects demonstrated reinfection with a different viral strain from the original infected strain.

There are missed pieces of information to interpret these data, but in line with previous studies, they suggest that pegIFN is effective for the treatment of acute HCV infection. Questions arise regarding the appropriateness of treating IDU given the substantial losses and occurrence of reinfections during treatment.

More articles on Acute HCV Infection

11/28/05

Reference
C Wang and others. Randomized trial of pegylated interferon for the treatment of acute HCV in Seattle injection drug users. Abstract 1210. 56th annual meeting of the American Association for the Study of Liver Diseases. November 11-15, 2005. San Francisco, CA.