Skip to main content
. 2019 May 10;35(3):559–565. doi: 10.3904/kjim.2018.338

Table 4.

Summary of studies related to sofosbuvir-based regimens in patients with severe renal impairment including cohorts with HCV GT2-infected patients

Regimens (%) GT (%) SVR12, % No. of HD SVR12 or SVR24 in HD Pts AEs in HD Pts Reference
SOF/SMV (17) 1 (90) 83 12 GT1 81.8% Anemia Desnoyer et al. (2016) [15]
SOF/LDV (8) 2 (10)
SOF/DCV (33)
SOF TIW/DCV (33)
SOF TIW/RBV (8)
SOF/PEG/RBV (18) 1 (72) 88 5 100% Anemia Saxena et al. (2016) [18]
SOF/RBV (30) 2 (16) GT is not available
SOF/SMV (40) 3 (9)
SOF/SMV/RBV (11) Other (3)
SOF/LDV (62) 1 (72) 97 20 95% Anemia Cox-North et al. (2017) [19]
SOF/LDV/RBV (7) 2 (7) GT is not available
SOF/DCV (21) 3 (17)
SOF/DCV/RBV (3) Other (4)
SOF/RBV (7)
SOF/RBV (63) 1 (65) 95.2 62 GT1 97.5% Anemia Agarwal et al. (2017)[20]
SOF AD/RBV (3) 2 (2) GT3 94.4% Dyspepsia
SOF/DCV (10) 3 (29)
SOF AD/RBV (24) Other (4)

HCV, hepatitis C virus; GT, genotype; SVR, sustained virological response; HD, hemodialysis; Pts, patients; AE, adverse event; SOF, sofosbuvir; SMV, simeprevir; LDV, ledipasvir; DCV, daclatasvir; TIW, three times a week; RBV, ribavirin; PEG, pegylated interferon; AD, alternate day.