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
相关论文
共 50 条
  • [41] Systematic Review of Modelling Approaches for the Cost Effectiveness of Hepatitis C Treatment with Direct-Acting Antivirals
    Chhatwal, Jagpreet
    He, Tianhua
    Lopez-Olivo, Maria A.
    PHARMACOECONOMICS, 2016, 34 (06) : 551 - 567
  • [42] Predictors of long-term cryoglobulinemic vasculitis outcomes after HCV eradication with direct-acting antivirals in the real-life
    Gragnani, Laura
    Lorini, Serena
    Marri, Silvia
    Vacchi, Caterina
    Madia, Francesco
    Monti, Monica
    Ferri, Clodoveo
    Zignego, Anna Linda
    AUTOIMMUNITY REVIEWS, 2022, 21 (01)
  • [43] HCV treatment with direct acting antivirals improves the insulin sensitivity
    Alsebaey, Ayman
    Elhelbawy, Mostafa
    Abdel-Razek, Wael
    Hashim, Mohammed
    Elshenawy, Hassan
    Waked, Imam
    EXPERT REVIEW OF ANTI-INFECTIVE THERAPY, 2019, 17 (09) : 749 - 754
  • [44] Liver Fibrosis and Body Mass Index Predict Hepatocarcinogenesis following Eradication of Hepatitis C Virus RNA by Direct-Acting Antivirals
    Akuta, Norio
    Kobayashi, Masahiro
    Suzuki, Fumitaka
    Sezaki, Hitomi
    Fujiyama, Shunichiro
    Kawamura, Yusuke
    Hosaka, Tetsuya
    Kobayashi, Mariko
    Saitoh, Satoshi
    Suzuki, Yoshiyuki
    Arase, Yasuji
    Ikeda, Kenji
    Kumada, Hiromitsu
    ONCOLOGY, 2016, 91 (06) : 341 - 347
  • [45] Treatment rate for HCV in the direct-acting antivirals era in HIV co-infected patients: data from an Italian cohort
    Cuomo, Gianluca
    Puzzolante, Cinzia
    Lazzaretti, Claudia
    Guaraldi, Giovanni
    Borghi, Vanni
    Mussini, Cristina
    MINERVA MEDICA, 2018, 109 (03) : 203 - 210
  • [46] Interferon free therapy with direct acting antivirals for HCV
    Asselah, Tarik
    Marcellin, Patrick
    LIVER INTERNATIONAL, 2013, 33 : 93 - 104
  • [47] HCV RNA Viral Load Assessments in the Era of Direct-Acting Antivirals
    Cobb, Bryan
    Pockros, Paul J.
    Vilchez, Regis A.
    Vierling, John M.
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2013, 108 (04) : 471 - 475
  • [48] Prioritization of HCV treatment in the direct-acting antiviral era: An economic evaluation
    Martin, Natasha K.
    Vickerman, Peter
    Dore, Gregory J.
    Grebely, Jason
    Miners, Alec
    Cairns, John
    Foster, Graham R.
    Hutchinson, Sharon J.
    Goldberg, David J.
    Martin, Thomas C. S.
    Ramsay, Mary
    Hickman, Matthew
    JOURNAL OF HEPATOLOGY, 2016, 65 (01) : 17 - 25
  • [49] Direct-Acting Antivirals for the Treatment of Chronic Hepatitis C: Open Issues and Future Perspectives
    Chae, Hee Bok
    Park, Seon Mee
    Youn, Sei Jin
    SCIENTIFIC WORLD JOURNAL, 2013,
  • [50] Effectiveness of direct-acting antivirals in Hepatitis C virus infection in haemodialysis patients
    Abad, Soraya
    Vega, Almudena
    Rincon, Diego
    Hernandez, Eduardo
    Merida, Evangelina
    Macias, Nicolas
    Munoz, Raquel
    Milla, Monica
    Luno, Jose
    Manuel Lopez-Gomez, Juan
    NEFROLOGIA, 2017, 37 (02): : 158 - 163