Short‐duration treatment for chronic hepatitis C virus with daclatasvir, asunaprevir, beclabuvir and sofosbuvir ( FOUR FOUR ward study)

摘要

Abstract Background & Aims The phase 2, FOUR ward study ( NCT 02175966) investigated short‐duration therapy (4/6?weeks) with four direct‐acting antivirals ( DAA s) with distinct mechanisms of action in patients infected with hepatitis C virus ( HCV ) genotype‐1. Methods Non‐cirrhotic patients were randomized 1:1 to DCV ‐ TRIO (fixed‐dose daclatasvir 30?mg, asunaprevir 200?mg and beclabuvir 75?mg) twice‐daily?+?sofosbuvir 400?mg once‐daily for 4 or 6?weeks. The primary endpoint was sustained virological response at post‐treatment Week 12 ( SVR 12). Patients without SVR 12 were offered retreatment based on the DAA resistance profile at failure; patients with resistance to ≤1 DCV ‐ TRIO component received DCV ‐ TRIO ?+? RBV for 12?weeks. Results Twenty‐eight patients with HCV genotype‐1 were enrolled; 79% had genotype‐1a infection and median baseline HCV ‐ RNA levels were high (9?×?10 6 ? IU / mL ). Most patients had undetectable HCV ‐ RNA at end of treatment (96% [n=27/28]); however, relapse occurred in 77% (n=10/13) and 43% (n=6/14) treated for 4 and 6 weeks, leading to SVR 12 rates of 29% (n=4/14) and 57% (n=8/14) respectively. SVR 12 was higher in patients with lower baseline HCV ‐ RNA (2?million IU / mL , 71% [n=5/7]; ≥2?million IU / mL , 33% [n=7/21]). None of the 16 non‐ SVR 12 patients had NS 3 or NS 5B resistance‐associated substitutions ( RAS ) detected at failure. All 15 patients retreated with DCV ‐ TRIO ?+? RBV for 12?weeks achieved SVR 12. All regimens were well tolerated. Conclusions Short‐duration treatment with four DAA s with distinct mechanisms of action was insufficient for most patients with genotype‐1 infection and high baseline viraemia. Non‐ SVR 12 was not associated with emergence of NS 3 or NS 5B RAS and retreatment with DCV ‐ TRIO ?+? RBV for 12?weeks led to SVR in all patients.