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Copyright: ©Author(s) 2026.
World J Virol. Mar 25, 2026; 15(1): 114321
Published online Mar 25, 2026. doi: 10.5501/wjv.v15.i1.114321
Table 2 Efficacy of directly acting antiviral based therapy in patients with hepatitis c virus related decompensated cirrhosis
Ref.
Patient population
SVR rates
Additional comments
Premkumar et al[44], 20241152 patients with DC (87% GT-3)82%-90% with sofosbuvir + velpatasvir + ribavirin or sofosbuvir + daclatasvir + ribavirinProbably the largest study showing effect of directly acting antivirals in DC and GT-3
Belperio et al[45], 2019243 patients with GT-3 related DC87.5%-100% in various arms with sofosbuvir + daclatasvir/velpatasvir with or without ribavirinHigher SVR (up to 92%) in patients with compensated cirrhosis
Lim et al[46], 2018667 patients with GT-1, 231 non-transplanted GT87.5%-100% with ledipasvir + sofosbuvir with or without ribavirinHigher SVR with compensated cirrhosis and in patients having normal bilirubin with high albumin
Manns et al[47], 2016333 patients with DC, with GT-1 and 4CTP-B: 87%-96%, CTP-C: 78%-85%17 patients died during the study period
Poordad et al[48], 201660 patients with advanced cirrhosisCTP-A: 93%, CTP-B: 93%, CTP-C: 56%, regimen used-sofosbuvir + daclatasvir + ribavirinPresence of DC was a negative predictor of SVR
Reddy et al[49], 2017240 patients with model for end stage liver disease score more than 1035%-84% with sofosbuvir + simeprevir + ribavirin or sosfosbuvir + ribavirinLow SVR rates with GT-1a; SVR only 35% with GT-3
Curry et al[50], 2015267 patients with DC, GT-3: 13%, GT-1: 75%Sofosbuvir + velpatasvir-24 weeks (86%), sofosbuvir + velpatasvir-12 weeks (83%), sofosbuvir + velpatasvir + ribavirin (94%)Serious adverse events in 16%-19%
Charlton et al[51], 2015337 DC patients with GT-186%-89% with sofosbuvir + ledipasvir + ribavirin for 12-24 weeksAll but 1 patient with GT-1


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