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Copyright ©2014 Baishideng Publishing Group Inc.
World J Gastroenterol. Jul 28, 2014; 20(28): 9253-9260
Published online Jul 28, 2014. doi: 10.3748/wjg.v20.i28.9253
Table 2 Available data from the studies in extenso on the use of direct-acting antiviral agents in the post-liver transplantation setting
Pungpapong et al[44]Coilly et al[45]Werner et al[46]Werner et al[48]
Patients (n)6037914
Baseline characteristics
Regimen (n)
TLV3519914
BCV251800
Four-week lead-in phase100%100%0%0%
IS therapy (n)
TAC31546
CSA652246
SIR1012
Fibrosis stage (n)
FO-F2312067
F3-F4381737
Cholestatic hepatitis (n)NA61NA
Results
HCV-RNA negative
Week 4NA51% (19/37)44% (4/9)43% (6/14)
Week 8NANANANA
Week 1291% (55/60)73% (27/37)89% (8/9)71% (10/14)
Week 2456% (24/43)NANA57% (8/14)
Week 48NA61% (17/28)NA50% (7/14)
Adverse events
Hematological AEs
Anemia93%92%66%71%
Leukopenia77%40%22%36%
Thrombocytopenia12%32%44%64%
Infectious complication12%27%11%14%
Renal insufficiency38%13%11%7%
Acute rejection5%NA0%7%
Dermatological toxicity10%5%33%NA
Hepatic decompensation12%NA0%7%
Death3%8%0%7%