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Early hepatitis C viral kinetics correlate with long-term outcome in patients receiving high dose induction followed by combination interferon and ribavirin therapy
- Source :
- Journal of Hepatology. 37:124-130
- Publication Year :
- 2002
- Publisher :
- Elsevier BV, 2002.
-
Abstract
- Background/Aims : The majority of patients with genotype 1 do not respond to interferon (IFN) plus ribavirin. Limited data exist on the use of induction followed by combination therapy. Methods : In this prospective study of 28 patients infected with genotype 1, randomization involved either daily or twice daily high dose IFN for 6 weeks, followed by standard therapy of 3 million units three times a week in combination with ribavirin for an additional 42 weeks. Hepatitis C virus (HCV) RNA was quantitated before and frequently during treatment. Results : The best correlate of response was δ (the infected cell loss rate). Sixteen patients continued on the study because they had at least a 2 log drop in their HCV RNA levels by week 12; all but one were PCR negative for HCV RNA at 48 weeks, and 14 of these 16 patients continued to be PCR negative at 72 weeks. Both African-Americans in our trial failed to respond to therapy, and differences were evident during the induction phase. Conclusions : This randomized study of induction IFN therapy followed by combination IFN plus ribavirin yielded the highest rate of sustained response (50%) reported to date in chronically HCV-infected patients with genotype 1. The predictive value of the infected cell loss rate needs to be evaluated prospectively in larger studies, particularly in patients receiving pegylated IFN.
- Subjects :
- medicine.medical_specialty
Hepatology
biology
Combination therapy
business.industry
Ribavirin
Hepacivirus
Hepatitis C virus
Hepatitis C
biology.organism_classification
medicine.disease
medicine.disease_cause
Gastroenterology
chemistry.chemical_compound
Pharmacotherapy
chemistry
Interferon
Internal medicine
Immunology
medicine
business
Prospective cohort study
medicine.drug
Subjects
Details
- ISSN :
- 01688278
- Volume :
- 37
- Database :
- OpenAIRE
- Journal :
- Journal of Hepatology
- Accession number :
- edsair.doi...........f43ba62e5deca52ac6097de0cea95024