Telaprevir- and boceprevir-based tritherapies in real practice for F3-F4 pretreated hepatitis C virus patients

被引:13
|
作者
Bonnet, Delphine [1 ]
Guivarch, Matthieu [1 ]
Berard, Emilie [2 ,3 ]
Combis, Jean-Marc [4 ]
Remy, Andre Jean [5 ]
Glibert, Andre [6 ]
Payen, Jean-Louis [7 ]
Metivier, Sophie [8 ]
Barange, Karl [8 ]
Desmorat, Herve [9 ]
Palacin, Anais [1 ]
Nicot, Florence [10 ]
Abravanel, Florence [10 ]
Alric, Laurent [1 ,11 ]
机构
[1] Purpan Univ Hosp, Internal Med Digest Dept, F-31059 Toulouse 9, France
[2] Toulouse Univ Hosp, Dept Epidemiol Hlth Econ & Publ Hlth, F-31073 Toulouse, France
[3] Toulouse III Univ, UMR 1027, INSERM, F-31062 Toulouse, France
[4] Clin Ambroise Pare, F-31300 Toulouse, France
[5] Perpignan Gen Hosp, F-66000 Perpignan, France
[6] Tarbes Gen Hosp, F-65000 Tarbes, France
[7] Montauban Gen Hosp, F-82000 Montauban, France
[8] Purpan Univ Hosp, Hepatogastroenterol Digest Dept, F-31059 Toulouse 9, France
[9] Clin Parc, F-31078 Toulouse 4, France
[10] INSERM, U1043, Virol Unit, F-310599 Toulouse 9, France
[11] Toulouse III Univ, UMR152, IRD, F-31400 Toulouse, France
关键词
Hepatitis C virus; Hepatitis C; Antiviral therapy; Protease inhibitors; Fibroscan; Liver stiffness; Cirrhosis; Boceprevir; Telaprevir; Ribavirin;
D O I
10.4254/wjh.v6.i9.660
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To assess, in a routine practice setting, the sustained virologic response (SVR) to telaprevir (TPV) or boceprevir (BOC) in hepatitis C virus (HCV) nullresponders or relapsers with severe liver fibrosis. METHODS: One hundred twenty-five patients were treated prospectively for 48 wk with TPV or BOC + pegylated-interferon (peg-INF) alpha 2a + ribavirin (PR) according to standard treatment schedules without randomization. These patients were treated in routine practice settings in 10 public or private health care centers, and the data were prospectively collected. Only patients with severe liver fibrosis (Metavir scores of F3 or F4 upon liver biopsy or liver stiffness assessed by elastography), genotype 1 HCV and who were null-responders or relapsers to prior PR combination therapy were included in this study. RESULTS: The Metavir fibrosis scores were F3 in 35 (28%) and F4 in 90 (72%) of the patients. In total, 62.9% of the patients were null-responders and 37.1% relapsers to the previous PR therapy. The overall SVR rate at 24 wk post-treatment withdrawal was 59.8%. The SVR was 65.9% in the TPV group and 44.1% in the BOC group. Independent predictive factors of an SVR included a response to previous treatment, relapsers vs null-responders [OR = 3.9; (1.4, 10.6), P = 0.0084], a rapid virological response (RVR) [OR 6.9 (2.6, 18.2), P = 0.001] and liver stiffness lower than 21.3 kPa [OR = 8.2 (2.3, 29.5), P = 0.001]. During treatment, 63 patients (50.8%) had at least one severe adverse event (SAE) of grade 3 or 4. A multivariate analysis identified two factors associated with SAEs: female gender [OR = 2.4 (1.1, 5.6), P = 0.037] and a platelet count below 150 x 103/mm(3) [OR = 5.3 (2.3, 12.4), P = 0.001]. CONCLUSION: More than half of these difficult-totreat patients achieved an SVR and had SAEs in an actual practice setting. The SVR rate was influenced by the response to previous PR treatment, the RVR and liver stiffness. (C) 2014 Baishideng Publishing Group Inc. All rights reserved.
引用
收藏
页码:660 / 669
页数:10
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