Sofosbuvir for hepatitis C genotype 2 or 3 in patients without treatment options.
By I. Jacobson, S. Gordon, Kris V. Kowdley, Eric M. Yoshida, M. Rodríguez-Torres, M. Sulkowski, M. Shiffman, E. Lawitz, G. Everson, M. Bennett and 13 more. New England Journal of Medicine, 2013
1,172 citations recorded by the source corpus.
Subfields: Emergency Medicine, Genetics, Hepatology
View Paper: https://www.semanticscholar.org/paper/22e8bafa516f1f0a449da3468e796ecf3d1838a6
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Citations in the corpus
- Sofosbuvir and ribavirin in HCV genotypes 2 and 3. (2014, neutral): “No response†† 18 (21) 10 (14) 4 (36) 41 (16)”
- EASL Recommendations on Treatment of Hepatitis C 2016. (2017, methodology): “When comparing 12 and 16 weeks of therapy in the FUSION trial [31], SVR was achieved in 82% (32/39) and 89% (31/35) of cases, respectively, 60% (6/10) and 78% (7/9) in patients with cirrhosis, respectively.”
- Hepatitis C Guidance 2019 Update: AASLD-IDSA Recommendations for Testing, Managing, and Treating Hepatitis C Virus Infection (2019, methodology): “(286) The use of sofosbuvir plus ribavirin is further supported by clinical trial data involving adolescents(287) and adults with genotype 2 or 3 infection.(288-291) At the time of manuscript preparation, sofosbuvir (plus ribavirin) remained the only FDA-approved DAA for children 3-11 years with gen”
- All-Oral 12-Week Treatment With Daclatasvir Plus Sofosbuvir in Patients With Hepatitis C Virus Genotype 3 Infection: ALLY-3 Phase III Study (2015, methodology): “The all-oral combination of SOF plus RBV requires 24 weeks of treatment because 12- and 16-week treatment durations were associated with lower response rates (30%-61% and 62%, respectively) in genotype 3– infected patients.(7,13,14) With 24-week treatment, lower response rates were observed in genot”
- Global Distribution and Prevalence of Hepatitis C Virus Genotypes (2014, background): “Genotype 3, however, which accounts for 30% of global infections, is not susceptible to the first generation of DAA protease inhibitors, and also appears less susceptible than other genotypes to sofosbuvir, the most advanced second-generation DAA therapy to date.(33,34) Ultimately, should DAA therap”
- EASL Recommendations on Treatment of Hepatitis C 2018. (2018, methodology): “When comparing 12 and 16 weeks of therapy in the FUSION trial [31], SVR was achieved in 82% (32/39) and 89% (31/35) of cases, respectively, 60% (6/10) and 78% (7/9) in patients with cirrhosis, respectively.”
- Ledipasvir and sofosbuvir for untreated HCV genotype 1 infection. (2014, neutral): “Insomnia 17 (8) 45 (21) 26 (12) 47 (22)”
- EASL Recommendations on Treatment of Hepatitis C 2015. (2015, methodology): “When comparing 12 and 16 weeks of therapy in the FUSION trial [46], SVR was achieved in 30% (19/64) and 62% (39/63) of cases, respectively, 19% (5/26) and 61% (14/23) in patients with cirrhosis, respectively.”