The practical management of chronic hepatitis C infection in Japan - dual therapy of daclatasvir plus asunaprevir

被引:4
作者
Hayes, C. Nelson [1 ,2 ]
Imamura, Michio [1 ,2 ]
Chayama, Kazuaki [1 ,2 ,3 ]
机构
[1] Hiroshima Univ, Inst Biomed & Hlth Sci, Dept Gastroenterol & Metab, Appl Life Sci,Minami Ku, 1-2-3 Kasumi, Hiroshima 7348551, Japan
[2] Hiroshima Univ, Liver Res Project Ctr, Hiroshima, Japan
[3] RIKEN, Ctr Genom Med, Lab Digest Dis, Hiroshima, Japan
关键词
Direct-acting antiviral agents; interferon-free therapy; NS5A inhibitor; polymerase inhibitor; protease inhibitor; resistance-associated variants; sustained virological response; NS3 PROTEASE INHIBITOR; GENOTYPE 1B INFECTION; SUSTAINED VIROLOGICAL RESPONSE; VIRUS NS5A INHIBITORS; HEPATOCELLULAR-CARCINOMA; HEMODIALYSIS-PATIENTS; COMBINATION THERAPY; RESISTANCE ANALYSIS; DIALYSIS PATIENTS; RANDOMIZED-TRIAL;
D O I
10.1080/17474124.2017.1270205
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction: Without treatment, many of the 200 million people worldwide with chronic hepatitis C virus (HCV) infection will develop cirrhosis or liver cancer. Japan was the first nation to approve an interferon-free therapy for HCV, and sustained viral response (SVR) rates >90% have been achieved with asunaprevir, a protease inhibitor, plus daclatasvir, an inhibitor of the non-structural 5A (NS5A) protein.Areas covered: This review provides an overview of the results from both clinical trials and real world experience with asunaprevir and daclatasvir therapy focused primarily on Japan. A literature search using the keywords asunaprevir,' daclatasvir,' interferon-free therapy,' and direct-acting antiviral drugs' was initially used to select relevant literature for inclusion in the review.Expert commentary: While not approved in the United States, dual therapy with asunaprevir plus daclatasvir has already been successfully used in Japan and throughout East Asia to treat many thousands of patients. Pre-existing or treatment-emergent NS5A-Y93 or -L31 resistance-associated variants (RAVs) may lead to viral breakthrough, and alternative therapies should be considered for these patients, but patients who harbor NS5A RAVs only at low frequency are likely to achieve SVR. The therapy has also been shown to be safe and effective with renal dysfunction or liver cirrhosis.
引用
收藏
页码:103 / 113
页数:11
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