New England Journal of Medicine· 2014Q1
Ledipasvir and Sofosbuvir for Previously Treated HCV Genotype 1 Infection
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- Q1SCImago
- 2014year
Short summary
A 12-week regimen of ledipasvir-sofosbuvir achieved a 94% sustained virologic response rate in patients with HCV genotype 1 who failed prior interferon-based therapy.
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Key points
- Ledipasvir-sofosbuvir achieved a 94% sustained virologic response (SVR) at 12 weeks post-treatment in patients with HCV genotype 1 who failed prior therapy.
- SVR rates increased to 99% with a 24-week treatment duration of ledipasvir-sofosbuvir.
- Adding ribavirin to ledipasvir-sofosbuvir did not significantly improve SVR rates (96% for 12 weeks, 99% for 24 weeks).
- No patients discontinued treatment due to adverse events, with fatigue, headache, and nausea being the most common side effects.
AI-generated from the title and abstract; the full text is not read.
Abstract
BACKGROUND: Effective treatment for hepatitis C virus (HCV) genotype 1 infection in patients who have not had a sustained virologic response to prior interferon-based therapy represents an unmet medical need. METHODS: We conducted a phase 3, randomized, open-label study involving patients infected with HCV genotype 1 who had not had a sustained virologic response after treatment with peginterferon and ribavirin, with or without a protease inhibitor. Patients were randomly assigned to receive the NS5A inhibitor ledipasvir and the nucleotide polymerase inhibitor sofosbuvir in a once-daily, fixed-dose combination tablet for 12 weeks, ledipasvir-sofosbuvir plus ribavirin for 12 weeks, ledipasvir-sofosbuvir for 24 weeks, or ledipasvir-sofosbuvir plus ribavirin for 24 weeks. The primary end point was a sustained virologic response at 12 weeks after the end of therapy. RESULTS: Among the 440 patients who underwent randomization and were treated, 20% had cirrhosis and 79% had HCV genotype 1a infection. The rates of sustained virologic response were high in all treatment groups: 94% (95% confidence interval [CI], 87 to 97) in the group that received 12 weeks of ledipasvir-sofosbuvir; 96% (95% CI, 91 to 99) in the group that received 12 weeks of ledipasvir-sofosbuvir and ribavirin; 99% (95% CI, 95 to 100) in the group that received 24 weeks of ledipasvir-sofosbuvir; and 99% (95% CI, 95 to 100) in the group that received 24 weeks of ledipasvir-sofosbuvir and ribavirin. No patient discontinued treatment owing to an adverse event. The most common adverse events were fatigue, headache, and nausea. CONCLUSIONS: Treatment with a once-daily, single-tablet regimen of ledipasvir and sofosbuvir resulted in high rates of sustained virologic response among patients with HCV genotype 1 infection who had not had a sustained virologic response to prior interferon-based treatment. (Funded by Gilead Sciences; ION-2 ClinicalTrials.gov number, NCT01768286.).
The authors' abstract, as published at the source. New England Journal of Medicine, 2014 · DOI ↗
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Field: Hepatology
HepatologyMedicine