1. R4 김슬기 /prof 김병호 Eric Lawitz, Jay P Lalezari, Tarek Hassanein, Kris V Kowdley, Fred F Poordad

2. Background  Protease inhibitors (Telaprevir, boceprevir: NS3/4A PI)  Restriction:Dosing, Resistance, Drug interactions, Side-effects  Sofosbuvir - Uridine nucleotide analogue Inhibitor of NS5B-directed HCV RNA replication in vitro. Prodrug of 2 ′ -deoxy-2 ′ -fluoro-2 ′ -C-methyluridine monophosphate that is converted within hepatocytes to its active uridine triphosphate form Causing chain termination during replication of the viral genome  We assessed the safety and efficacy of sofosbuvir, a uridine nucleotide analogue, in tr eatment-naive patients with genotype 1–3 HCV infection

3. Methods Two-cohort, phase 2 trial HCV genotype 1 (cohort A) -Sofosbuvir 200 mg, sofosbuvir 400 mg, placebo (2:2:1) for 12 weeks in combination with peginterferon (180 μ g per week) and ribavirin (1000–1200 mg daily) -continued peginterferon and ribavirin for an additional 12 weeks or 36 weeks (depending on viral response) HCV genotypes 2 or 3 (cohort B) -sofosbuvir 400 mg plus peginterferon and ribavirin for 12 weeks  primary outcomes :safety and tolerability  Secondary outcomes : Efficacy - RVR (HCV RNA <15 IU/mL at week 4 of treatment) - eRVR (HCV RNA <15 IU/mL from weeks 4–12 ) - SVR12/24(HCV RNA ≤ 15 IU/mL at 12 /24weeks after completion of treatment )

4. Study design and participants Treatment-naive patients with HCV genotypes 1–3 from 22 centres,USA Aug 16, 2010, and Dec 13, 2010 Age:18–70 years old HCV RNA concentration ≥50 000 IU/mL No cirrhosis. Inclusion criteria : Neutrophil count of 1·5 × 10 9 /L (or ≥1·25 × 10 9 /L for black patients) Haemoglobin concentration ≥ 11 g/dL (women) or ≥ 12 g/dL (men) Platelet count ≥ 90 × 10 9 /L Total bilirubin ≤ two times ULN(21 μ mol/L) Albumin ≤ 3.0 g/dL Exclusion: HBV, HIV, psychiatric illness, pulmonary or cardiac disease, seizure disorder, other serious comorbid disorders

5. Randomisation and masking We randomly assigned patients (2:2:1) with HCV-1 infection (cohort A) computer-generated randomisation sequence Randomisation was stratified by - -IL28B rs12979860 single nucleotide polymorphism genotype (CC or non-CC) - -Baseline HCV RNA (<800 000 IU/mL or ≥800 000 IU/mL) All patients concurrently received open-label peginterferon and ribavirin. Investigators and patients were masked to HCV RNA results and treatment allocation until week 12. All patients who achieved eRVR were unmasked before their visit at week 24 to ensure that any patients allocated to placebo were scheduled to continue treatment until week 48 unless stopping criteria were met Cohort B- non-randomised, open label rs8099917(T/G): TT vs TG/GG rs12979860(C/T):CC vs CT/TT

6. Procedures Peginterferon 180 μ g per week s.c Ribavirin dose according to weight (patients <75 kg received 1000 mg and those ≥75 kg received 1200 mg ) HCV RNA measuring : COBAS AmpliPrep/COBAS Taqman HCV test (Roche; Indianapolis, IN, USA) with a limit of detection of 15 IU/mL. All laboratory testing : Cenetron Laboratories (Austin, TX, USA). Resistance monitoring : Breakthrough, Relapse -Breakthrough :HCV RNA ≥15 IU/mL on treatment after having previously had HCV RNA <15 IU/mL on treatment, confirmed with two consecutive values or last available measurement; -Relapse :HCV RNA ≥15 IU/mL during the post-treatment period having achieved HCV RNA <15 IU/mL at end of treatment, confirmed with two consecutive values or last available measurement Use of erythropoietin-stimulating agents or granulocyte colony-stimulating factor -only after the 12 weeks of sofosbuvir or placebo dosing.

7. eRVR  12 additional weeks of peginterferon and ribavirin Reduction in HCV RNA ≥ 2 log 10 by week 12, but was not below the limit of detection  continued their treatment until week 24. Not achieve an eRVR, receiving placebo  additional 36 weeks of treatment with peginterferon and ribavirin. Reduction in HCV RNA ≤ 2 log 10 at week 12  discontinued patients’ treatment HCV RNA detectable at week 24  discontinued treatment with peginterferon and ribavirin. Genotype 2 or 3 in which all patients received open-label sofosbuvir 400 mg with peginterferon and ribavirin for 12 weeks, with no response-guided treatment.

8. Result

9. (4%)(6%)(12%)

10. Base line characteristics

11. <

13. Figure 2: Mean concentrations of hepatitis C virus RNA during the 12 weeks of sofosbuvir treatment

14. baseline HCV RNA >800 000 IU/mL CT IL28B allele. protease inhibitors vs peginterferon and ribavirin control telaprevir (75% vs 44%) and boceprevir (67–68% vs 40%).

15. Conclusion  Our findings lend support to the further assessment, in phase 2 and 3 trials, of sofosbuvir 400 mg plus peginterferon and ribavirin for 12 weeks in treatment- naive patients with HCV genotype-1.