TY - JOUR
T1 - Retreatment of patients with treatment failure of directacting antivirals
T2 - Focus on hepatitis C virus genotype 1b
AU - Kanda, Tatsuo
AU - Nirei, Kazushige
AU - Matsumoto, Naoki
AU - Higuchi, Teruhisa
AU - Nakamura, Hitomi
AU - Yamagami, Hiroaki
AU - Matsuoka, Shunichi
AU - Moriyama, Mitsuhiko
N1 - Publisher Copyright:
© The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved.
PY - 2017/12/14
Y1 - 2017/12/14
N2 - The recent development of direct-Acting antiviral agents (DAAs) against hepatitis C virus (HCV) infection could lead to higher sustained virological response (SVR) rates, with shorter treatment durations and fewer adverse events compared with regimens that include interferon. However, a relatively small proportion of patients cannot achieve SVR in the first treatment, including DAAs with or without peginterferon and/or ribavirin. Although retreatment with a combination of DAAs should be conducted for these patients, it is more difficult to achieve SVR when retreating these patients because of resistance-Associated substitutions (RASs) or treatment-emergent substitutions. In Japan, HCV genotype 1b (GT1b) is founded in 70% of HCVinfected individuals. In this minireview, we summarize the retreatment regimens and their SVR rates for HCV GT1b. It is important to avoid drugs that target the regions targeted by initial drugs, but next-generation combinations of DAAs, such as sofosbuvir/velpatasvir/ voxilaprevir for 12 wk or glecaprevir/pibrentasvir for 12 wk, are proposed to be potential solution for the HCV GT1b-infected patients with treatment failure, mainly on a basis of targeting distinctive regions. Clinicians should follow the new information and resources for DAAs and select the proper combination of DAAs for the retreatment of HCV GT1b-infected patients with treatment failure.
AB - The recent development of direct-Acting antiviral agents (DAAs) against hepatitis C virus (HCV) infection could lead to higher sustained virological response (SVR) rates, with shorter treatment durations and fewer adverse events compared with regimens that include interferon. However, a relatively small proportion of patients cannot achieve SVR in the first treatment, including DAAs with or without peginterferon and/or ribavirin. Although retreatment with a combination of DAAs should be conducted for these patients, it is more difficult to achieve SVR when retreating these patients because of resistance-Associated substitutions (RASs) or treatment-emergent substitutions. In Japan, HCV genotype 1b (GT1b) is founded in 70% of HCVinfected individuals. In this minireview, we summarize the retreatment regimens and their SVR rates for HCV GT1b. It is important to avoid drugs that target the regions targeted by initial drugs, but next-generation combinations of DAAs, such as sofosbuvir/velpatasvir/ voxilaprevir for 12 wk or glecaprevir/pibrentasvir for 12 wk, are proposed to be potential solution for the HCV GT1b-infected patients with treatment failure, mainly on a basis of targeting distinctive regions. Clinicians should follow the new information and resources for DAAs and select the proper combination of DAAs for the retreatment of HCV GT1b-infected patients with treatment failure.
KW - Direct-Acting antiviral agent
KW - Genotype 1b
KW - Hepatitis c virus
KW - Resistance-Associated substitutions
UR - http://www.scopus.com/inward/record.url?scp=85038439237&partnerID=8YFLogxK
U2 - 10.3748/wjg.v23.i46.8120
DO - 10.3748/wjg.v23.i46.8120
M3 - Review article
C2 - 29290649
AN - SCOPUS:85038439237
SN - 1007-9327
VL - 23
SP - 8120
EP - 8127
JO - World Journal of Gastroenterology
JF - World Journal of Gastroenterology
IS - 46
ER -