![]() |
3rd International AIDS Society Conference on HIV Pathogenesis and TreatmentRio de Janeiro - July 24 - 27, 2005 |
EFFICACY OF ACUTE HCV TREATMENT WITH PEG-INTERFERON α-2B AND RIBAVIRIN IN HIV INFECTED PATIENTS
IAS Conf HIV Pathog Treat 2005 Jul 24-27;3rd: Abstract No. TuPe1.1C01
Kruk A.
Peoples Friendship University of Russia, Moscow, Russian Federation
INTRODUCTION: Mortality and morbidity associated with Hepatitis C (HCV) is increasingly affecting the HIV/HCV co-infected population. It's essential to perform clinical studies to identify the efficacy, safety and tolerability of interferon and ribavirin in the co-infected population.
METHODS: Efficacy, safety and tolerability of peg-interferon α-2b 1.5mcg/kg/weekly and ribavirin 800-1000mg/d for 24 weeks was assessed in a prospective open labeled study in HIV-infected patients with acute HCV-infection. Quantitative HCV RNA, HIV RNA and CD4 count as well as blood count and liver enzymes were assessed at baseline and at weeks 4, 12, 24, 48. All patients had a CD4 count >200×10/ml and HIV viral load <200 cp/ml. Recruitment of patients is ongoing with 17 patients enrolled to date.
RESULTS: Infection was predominantly acquired through intravenous drug usage (87%). Other groups were heterosexuals (8%) and homosexuals (5%). The majority was virologically stable on HAART (53%); the rest didn't require HAART. 31% patients were infected with genotype 1/4 and 69% with genotype 2/3. 79% were male and mean age was 29 years (range 19-39). At 4 weeks early biochemical and virological response (normalization of liver transaminases and negative HCV RNA) was observed in 11 (65%) patients, and at 12 weeks 15 (88%) patients were HCV RNA negative. 2 patients (12%) didn't complete therapy up to 3 months due to severe depression. At the end of treatment 15 (88%) patients were still HCV RNA negative, and 9 (53%) patients who overcame 48 weeks are always HCV RNA negative.
CONCLUSIONS: After 24 weeks of acute HCV treatment with peg-interferon α-2b and ribavirin 15 (88%) of treated patients were HCV RNA negative. Peg-interferon and ribavirin show good antiviral efficacy in HIV/HCV co-infected patients. Discontinuation rate is low, but depression is a major problem in this cohort with a high proportion of drug users.
Download PDF of this abstract.
050724
Clinical | TuPe1.1C01 | Alexey Kruk
Hepatitis viruses
Copyright © 2005 - International AIDS Society (IAS). All information and content relating to the abstracts from the 3rd International AIDS Society Conference on HIV Pathogenesis and Treatment, such as text, graphics, logos, button icons, images, audio clips, and software is protected by copyright. Permission is hereby granted for the non-commercial use or reproduction of the information on this web site, provided that the use of such information is accompanied by an acknowledgement that IAS is the source of the information and the name of the author of the article.
AEGiS is made possible through unrestricted funding from Boehringer Ingelheim, Bridgestone/Firestone Charitable Trust, Bristol-Myers Squibb Company, Elton John AIDS Foundation, the National Library of Medicine, and donations from users like you. Always watch for outdated information. This article first appeared in 2005. This material is designed to support, not replace, the relationship that exists between you and your doctor.
AEGiS presents published material, reprinted with permission and neither endorses nor opposes any material. All information contained on this website, including information relating to health conditions, products, and treatments, is for informational purposes only. It is often presented in summary or aggregate form. It is not meant to be a substitute for the advice provided by your own physician or other medical professionals. Always discuss treatment options with a doctor who specializes in treating HIV.
Copyright ©1980, 2005. AEGiS. All materials appearing on AEGiS are protected by copyright as a collective work or compilation under U.S. copyright and other laws and are the property of AEGiS, or the party credited as the provider of the content. Permission is hereby granted for the non-commercial use or reproduction of the information herein, provided that the use of such information is accompanied by an acknowledgement that IAS is the source of the information and the name of the author of the article.