Randomized Clinical Trial
Copyright ©The Author(s) 2018.
World J Gastroenterol. Mar 28, 2018; 24(12): 1361-1372
Published online Mar 28, 2018. doi: 10.3748/wjg.v24.i12.1361
Figure 1
Figure 1 SVR12 in the immediate treatment arm. 1Includes the patient with genotype 1a infection; 2On-treatment HCV RNA ≥ LLOQ after < LLOQ, or increased > 1 log10 over nadir; 3Posttreatment HCV RNA ≥ LLOQ after < LLOQ without detectable target at EOT. EOT: End of treatment; HCV: Hepatitis C virus; LLOQ: Lower limit of quantitation; SVR12: Sustained virologic response at post-treatment week 12.
Figure 2
Figure 2 SVR12 according to selected baseline characteristics in the immediate treatment arm. HCV: Hepatitis C virus; SVR12: Sustained virologic response at posttreatment week 12.
Figure 3
Figure 3 SVR12 in the placebo-deferred treatment arm. 1On-treatment HCV RNA ≥ LLOQ after < LLOQ, or increased >1 log10 over nadir; 2HCV RNA < LLOQ (TND) at EOT followed by HCV RNA ≥ LLOQ at any follow-up visit; 3Other nonresponders included patients who had HCV RNA < LLOQ (TND) at EOT, but with missing posttreatment week 12 data; 4Death, not considered related to study therapy (stab wound). EOT: End of treatment; HCV: Hepatitis C virus; LLOQ: Lower limit of quantitation; SVR12, Sustained virologic response at post-treatment week 12.
Figure 4
Figure 4 SVR12 according to selected baseline characteristics in the placebo-deferred treatment arm1. 1Reasons for patients not achieving SVR12 included virologic breakthrough (n = 7), relapse (n = 1) or other (n = 1; death, not considered related to study therapy). HCV: Hepatitis C virus; SVR12: Sustained virologic response at post-treatment week 12.