Grazoprevir and elbasvir plus ribavirin for chronic HCV genotype-1 infection after failure of combination therapy containing a direct-acting antiviral agent

被引:120
作者
Forns, Xavier [1 ,2 ]
Gordon, Stuart C. [3 ]
Zuckerman, Eli [4 ]
Lawitz, Eric [5 ]
Calleja, Jose L. [6 ]
Hofer, Harald [7 ]
Gilbert, Christopher [8 ]
Palcza, John [8 ]
Howe, Anita Y. M. [8 ]
DiNubile, Mark J. [8 ]
Robertson, Michael N. [8 ]
Wahl, Janice [8 ]
Barr, Eliav [8 ]
Buti, Maria [2 ,9 ]
机构
[1] Hosp Clin Barcelona, Liver Unit, IDIBAPS, E-08036 Barcelona, Spain
[2] CIBEREHD, Barcelona, Spain
[3] Henry Ford Hlth Syst, Detroit, MI USA
[4] Carmel Hosp, Haifa, Israel
[5] Univ Texas Hlth Sci Ctr San Antonio, Texas Liver Inst, San Antonio, TX 78229 USA
[6] Univ Autonoma Madrid, Hosp Univ Puerta de Hierro, Serv Gastroenterol & Hepatol, Madrid, Spain
[7] Med Univ Vienna, Div Gastroenterol & Hepatol, Vienna, Austria
[8] Merck & Co Inc, Kenilworth, NJ USA
[9] Hosp Univ Valle Hebron, Barcelona, Spain
关键词
C-SALVAGE; HCV genotype-1; Grazoprevir; Elbasvir; Direct-acting antiviral agents; HEPATITIS-C VIRUS; TREATMENT-NAIVE PATIENTS; CLINICAL-RELEVANCE; RESISTANT VARIANTS; SOFOSBUVIR; ABT-450/R-OMBITASVIR; NONRESPONDERS; BOCEPREVIR; LEDIPASVIR; DASABUVIR;
D O I
10.1016/j.jhep.2015.04.009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: The Phase-2 C-SALVAGE study evaluated an investigational interferon-free combination of grazoprevir (a NS3/4A protease inhibitor) and elbasvir (a NS5A inhibitor) with ribavirin for patients with chronic HCV genotype-1 infection who had failed licensed DAA-containing therapy. Methods: C-SALVAGE was an open-label study of grazoprevir 100 mg and elbasvir 50 mg QD with weight-based ribavirin BID for 12 weeks in cirrhotic and non-cirrhotic patients with chronic HCV genotype-1 infection who had not attained SVR after >= 4 weeks of peginterferon and ribavirin plus either boceprevir, telaprevir, or simeprevir. Exclusion criteria included decompensated liver disease, hepatocellular carcinoma, and HIV or HBV co-infection. The primary efficacy outcome was SVR12 defined as a HCV RNA level below the assay limit of quantification 12 weeks after the end of treatment. Results: Of the 79 patients treated with >= 1 dose of study drug, 66 (84%) patients had a history of virologic failure on a regimen containing a NS3/4A protease inhibitor; 12 of the other 13 patients discontinued prior treatment because of adverse experiences. At entry, 34 (43.6%) of 78 evaluable patients harbored NS3 RAVs. SVR12 rates were 76/79 (96.2%) overall, including 28/30 (93.3%) patients with genotype 1a infection, 63/66 (95.5%) patients with prior virologic failure, 43/43 (100%) patients without baseline RAVs, 31/34 (91.2%) patients with baseline NS3 RAVs, 6/8 (75.0%) patients with baseline NS5A RAVs, 4/6 66.7%) patients with both baseline NS3 and RAVs, and 32/34 (94.1%) cirrhotic patients. None of the five reported serious adverse events were considered drug-related. Conclusions: Grazoprevir and elbasvir plus ribavirin for 12 weeks provides a promising new treatment option for patients after failure of triple therapy containing an earlier-generation protease inhibitor. (C) 2015 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:564 / 572
页数:9
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