Re-treatment of chronic hepatitis C virus genotype 1 infection after relapse: an open-label pilot study
Anu Osinusi, Anita Kohli, Miriam M Marti, Amy Nelson, Xiaozhen Zhang, Eric G Meissner, Rachel Silk, Kerry Townsend, Phillip S Pang, G Mani Subramanian, John G McHutchison, Anthony S Fauci, Henry Masur, Shyam Kottilil, Anu Osinusi, Anita Kohli, Miriam M Marti, Amy Nelson, Xiaozhen Zhang, Eric G Meissner, Rachel Silk, Kerry Townsend, Phillip S Pang, G Mani Subramanian, John G McHutchison, Anthony S Fauci, Henry Masur, Shyam Kottilil
Abstract
Background: The interferon (IFN)-free regimen of sofosbuvir and ribavirin for 24 weeks was recently approved to treat chronic hepatitis C virus (HCV) genotype 1 (GT-1) infection for patients ineligible for IFN. However, sofosbuvir plus ribavirin therapy is associated with relapse in 15% to 30% of patients with HCV GT-1. Neither the mechanism of relapse nor the optimal re-treatment strategy for these patients is defined.
Objective: To assess the safety and efficacy of sofosbuvir plus ledipasvir in patients with chronic HCV GT-1 that relapsed after sofosbuvir plus ribavirin therapy.
Design: Phase 2a, open-label study. (ClinicalTrials.gov: NCT01805882).
Setting: Single U.S site.
Patients: 14 patients with HCV GT-1 that relapsed after treatment with sofosbuvir plus ribavirin for 24 weeks were re-treated with sofosbuvir plus ledipasvir for 12 weeks.
Measurements: HCV RNA concentration and population sequencing to detect NS5B S282T mutations.
Results: All 14 patients treated with sofosbuvir plus ledipasvir for 12 weeks achieved a sustained virologic response, including 7 with advanced liver disease (Knodell Histology Activity Index score of 3 or 4) and 1 with a detectable NS5B S282T mutation after sofosbuvir plus ribavirin therapy. Sofosbuvir plus ledipasvir was well-tolerated with few adverse events. Four grade 3 events (elevated serum creatinine in a patient with baseline renal insufficiency, hypercholesterolemia, and hypophosphatemia) occurred. There were no grade 4 events or treatment discontinuations.
Limitation: Small sample size.
Conclusion: The fixed-dose combination of sofosbuvir plus ledipasvir was efficacious in a small cohort of patients with HCV GT-1 that relapsed after sofosbuvir plus ribavirin therapy, even in the setting of advanced liver disease. Larger studies are needed to confirm these preliminary efficacy results.
Primary funding source: National Institute of Allergy and Infectious Diseases, National Institutes of Health, National Cancer Institute, and Gilead Sciences.
Trial registration: ClinicalTrials.gov NCT00047385 NCT01805882 NCT00047385.
Source: PubMed