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
  • [21] Impact of HCV eradication following direct-acting antivirals on liver stiffness measurement: a prospective longitudinal study
    Ahmed El Ray
    Laurent Castera
    Ahmed Al-Ashry
    Sameh Ghali
    Egyptian Liver Journal, 13
  • [22] Peripheral neuropathy after viral eradication with direct-acting antivirals in chronic HCV hepatitis: A prospective study
    Zanone, Maria M.
    Marinucci, Claudia
    Ciancio, Alessia
    Cocito, Dario
    Zardo, Federica
    Spagone, Emanuela
    Ferrero, Bruno
    Cerruti, Cristina
    Charrier, Lorena
    Cavallo, Franco
    Saracco, Giorgio M.
    Porta, Massimo
    LIVER INTERNATIONAL, 2021, 41 (11) : 2611 - 2621
  • [23] Impact of HCV eradication following direct-acting antivirals on liver stiffness measurement: a prospective longitudinal study
    El Ray, Ahmed
    Castera, Laurent
    Al-Ashry, Ahmed
    Ghali, Sameh
    EGYPTIAN LIVER JOURNAL, 2023, 13 (01)
  • [24] The 'Viennese epidemic' of acute HCV in the era of direct-acting antivirals
    Chromy, David
    Bauer, David Jm
    Simbrunner, Benedikt
    Jachs, Mathias
    Hartl, Lukas
    Schwabl, Philipp
    Schwarz, Caroline
    Rieger, Armin
    Grabmeier-Pfistershammer, Katharina
    Mandorfer, Mattias
    Trauner, Michael
    Ferenci, Peter
    Gschwantler, Michael
    Reiberger, Thomas
    JOURNAL OF HEPATOLOGY, 2022, 77 : S555 - S555
  • [25] Letter: HBV/HCV coinfection in the era of direct-acting antivirals
    Hsu, C. -S.
    Wang, P. -C.
    Li, C. -H.
    Lin, H. H.
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2017, 46 (02) : 211 - 211
  • [26] NEW BLACK BOX WARNING FOR DIRECT-ACTING ANTIVIRALS FOR HCV
    Aschenbrenner, Diane S.
    AMERICAN JOURNAL OF NURSING, 2017, 117 (02) : 21 - 21
  • [27] The 'Viennese epidemic' of acute HCV in the era of direct-acting antivirals
    Chromy, David
    Bauer, David J. M.
    Simbrunner, Benedikt
    Jachs, Matthias
    Hartl, Lukas
    Schwabl, Philipp
    Schwarz, Caroline
    Rieger, Armin
    Grabmeier-Pfistershammer, Katharina
    Trauner, Michael
    Ferenci, Peter
    Mandorfer, Mattias
    Gschwantler, Michael
    Reiberger, Thomas
    JOURNAL OF VIRAL HEPATITIS, 2022, 29 (05) : 385 - 394
  • [28] Short duration of direct-acting antivirals for acute HCV infection
    Yu, Ming-Lung
    LANCET INFECTIOUS DISEASES, 2017, 17 (05): : 481 - 482
  • [29] Fibrosis improvement in patients with HCV treated with direct-acting antivirals
    McPhail, James
    Sims, Omar T.
    Guo, Yuqi
    Wooten, David
    Herndon, John S.
    Massoud, Omar I.
    EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2021, 33 (07) : 996 - 1000
  • [30] Direct-acting antivirals for RSV treatment, a review
    Bonneux, Brecht
    Jacoby, Edgar
    Ceconi, Martina
    Stobbelaar, Kim
    Delputte, Peter
    Herschke, Florence
    ANTIVIRAL RESEARCH, 2024, 229