A revolution in HCV treatment with direct-acting antivirals: From non-response to eradication

被引:6
|
作者
Asselah, Tarik [1 ,2 ]
机构
[1] Univ Paris 07, AP HP, Hepatol Dept, Clichy, France
[2] Beaujon Hosp, INSERM, U773, CRB3, Clichy, France
关键词
Interferon free regimen; NS5A inhibitors; Null response; Protease inhibitors; Immune response; Genotype; 1; REPLICATION COMPLEX INHIBITOR; GENOTYPE; INFECTION; PROTEASE INHIBITOR; BMS-790052; BMS-650032; RIBAVIRIN; THERAPY;
D O I
10.1016/j.jhep.2012.03.005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Patients with chronic hepatitis C virus (HCV) infection who have not had a response to therapy with peginterferon and ribavirin may benefit from the addition of multiple direct-acting antiviral agents to their treatment regimen. Methods: This open-label, phase 2a study included an exploratory cohort of 21 patients with chronic HCV genotype 1 infection who had not had a response to previous therapy (i.e., had not had >= 2 log(10) decline in HCV RNA after >= 12 weeks of treatment with peginterferon and ribavirin). We randomly assigned patients to receive the NS5A replication complex inhibitor daclatasvir (60 mg once daily) and the NS3 protease inhibitor asunaprevir (600 mg twice daily) alone (group A, 11 patients) or in combination with peginterferon alfa-2a and ribavirin (group B, 10 patients) for 24 weeks. The primary end point was the percentage of patients with a sustained virologic response 12 weeks after the end of the treatment period. Results: A total of 4 patients in group A (36%; 2 of 9 with HCV genotype 1 a and 2 of 2 with genotype 1b) had a sustained virologic response at 12 weeks after treatment and also at 24 weeks after treatment. Six patients (all with HCV genotype I a) had viral breakthrough while receiving therapy, and resistance mutations to both antiviral agents were found in all cases; 1 patient had a viral response at the end of treatment but had a relapse after the treatment period. All 10 patients in group B had a sustained virologic response at 12 weeks after treatment, and 9 had a sustained virologic response at 24 weeks after treatment. Diarrhea was the most common adverse event in both groups. Six patients had transient elevations of alanine aminotransferase levels to more than three times the upper limit of the normal range. Conclusions: This preliminary study involving patients with HCV genotype 1 infection who had not had a response to prior therapy showed that a sustained virologic response can be achieved with two direct-acting antiviral agents only. In addition, a high rate of sustained virologic response was achieved when the two direct-acting antiviral agents were combined with peginterferon alfa-2a and ribavirin. (Funded by Bristol-Myers Squibb; ClinicalTrials.gov number, NCT01012895.). (C) 2012 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:455 / 457
页数:3
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