Sustained virologic response of 100% in HCV genotype 1b patients with cirrhosis receiving ombitasvir/paritaprevir/r and dasabuvir for 12 weeks

被引:123
作者
Feld, Jordan J. [1 ]
Moreno, Christophe [2 ]
Trinh, Roger [3 ]
Tam, Edward [4 ]
Bourgeois, Stefan [5 ]
Horsmans, Yves [6 ]
Elkhashab, Magdy [7 ]
Bernstein, David E. [8 ]
Younes, Ziad [9 ]
Reindollar, Robert W. [10 ]
Larsen, Lois [3 ]
Fu, Bo [3 ]
Howieson, Kevin [3 ]
Polepally, Akshanth R. [3 ]
Pangerl, Andreas [3 ]
Shulman, Nancy S. [3 ]
Poordad, Fred [11 ]
机构
[1] Univ Toronto, Toronto Ctr Liver Dis, Toronto, ON, Canada
[2] Univ Libre Bruxelles, CUB Hop Erasme, Brussels, Belgium
[3] AbbVie Inc, N Chicago, IL USA
[4] LAIR Ctr, Vancouver, BC, Canada
[5] ZNA Stuivenberg, Antwerp, Belgium
[6] Catholic Univ Louvain, B-1200 Brussels, Belgium
[7] Toronto Liver Ctr, Toronto, ON, Canada
[8] N Shore Univ Hosp, Manhasset, NY USA
[9] GastroOne, Germantown, TN USA
[10] Piedmont Healthcare Carolinas Ctr Liver Dis, Statesville, NC USA
[11] Univ Texas Hlth Sci Ctr San Antonio, Texas Liver Inst, San Antonio, TX 78229 USA
关键词
Cirrhosis; Direct-acting antivirals; 3D; TURQUOISE-III; HEPATITIS-C; OPEN-LABEL; PEGYLATED INTERFERON; EXPERIENCED PATIENTS; GRAZOPREVIR MK-5172; ELBASVIR MK-8742; PLUS SOFOSBUVIR; TREATMENT-NAIVE; RIBAVIRIN; INFECTION;
D O I
10.1016/j.jhep.2015.10.005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background & Aims: Patients with chronic hepatitis C virus (HCV) infection and cirrhosis have a higher risk for liver-related complications and have historically been more difficult to cure than patients without cirrhosis. We evaluated the safety and efficacy of ombitasvir/paritaprevir/ritonavir and dasabuvir, without ribavirin, for 12 weeks in patients with HCV genotype 1b infection and compensated cirrhosis. Methods: Treatment-naive and peginterferon/ribavirin treatment-experienced patients received 12 weeks of ombitasvir/paritaprevir/ritonavir (25/150/100 mg once daily) and dasabuvir (250 mg twice daily). Key inclusion criteria were hemoglobin >= 10 g/dl, albumin >= 2.8 g/dl, platelet count >= 25 x 10(9)/L, creatinine clearance >= 30 ml/min, and Child-Pugh score <= 6. Efficacy was assessed by the percentage of patients achieving SVR (HCV RNA <25 IU/ml) 12 weeks post-treatment (SVR12). Efficacy and safety were assessed in all patients receiving study drug. Results: Sixty patients with HCV genotype 1b infection and cirrhosis received treatment. The study population comprised 62% male, 55% treatment-experienced, 83% with IL28B non-CC genotype, 22% with platelet count <90 x 10(9)/L, and 17% with albumin <3.5 g/dl. All 60 patients completed treatment, and SVR12 was achieved in 100% (95% CI, 94.0-100%) of patients. The most common adverse events were fatigue (22%), diarrhea (20%), and headache (18%). Only one patient (1.7%) experienced a serious adverse event. Laboratory abnormalities were infrequently observed and not clinically significant. Conclusions: The HCV regimen of ombitasvir/paritaprevir/ritonavir and dasabuvir without ribavirin for 12 weeks achieved 100% SVR12 and was well tolerated in HCV genotype 1b-infected patients with cirrhosis, suggesting that this 12-week ribavirin-free regimen is sufficient in this population. (C) 2015 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:301 / 307
页数:7
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