Back to Search Start Over

Sustained virological response with telaprevir in 1078 patients with advanced hepatitis C: The international telaprevir access program

Authors :
Colombo, Massimo
Iraqi, Wafae
DeMasi, Ralph
Hill, Andrew
Lonjon-Domanec, Isabelle
Wedemeyer, Heiner
Strasser, Simone
Moreno, Christophe
Ferreira, Paulo Abrao
Urbanek, Petr
Fernández, Inmaculada
Abdurakmonov, Djamal
Streinu-Cercel, Adrian
Verheyen, Anke
Colombo, Massimo
Iraqi, Wafae
DeMasi, Ralph
Hill, Andrew
Lonjon-Domanec, Isabelle
Wedemeyer, Heiner
Strasser, Simone
Moreno, Christophe
Ferreira, Paulo Abrao
Urbanek, Petr
Fernández, Inmaculada
Abdurakmonov, Djamal
Streinu-Cercel, Adrian
Verheyen, Anke
Source :
Journal of hepatology, 61 (5
Publication Year :
2014

Abstract

Background & Aims: There is little information regarding the extent to which difficult to cure patients with advanced liver fibrosis, due to hepatitis C virus genotype-1 (HCV-1) can successfully and safely be treated with triple therapy with telaprevir (TVR), pegylated interferon alpha (P) and ribavirin (R). In the TVR early access program HEP3002 we aimed to explore treatment safety and efficacy, and identify predictors of sustained virological response at week 24 (SVR24). Methods: 1078 patients with bridging fibrosis (n = 552) or cirrhosis (n = 526) diagnosed by either liver biopsy or non-invasive markers, with compensated bone marrow (neutrophils >1500/ mm3, Hb >12/13 g/dl) and liver function (Albumin >3.3 g/dl, Platelets >90,000/ml) received TVR PR for 12 weeks, followed by a PR tail according to label. Results: Overall, 614 (57%) achieved SVR24 by intention-to-treat analysis. The SVR24 rate was 68% in 221 treatment naïve patients (62.8% F4), 72% in 356 prior relapsers (64.4% F4), 55% in 139 partial responders (53.2% F4), and 34% in 294 null responders (28.6% F4). The SVR24 rate to response-guided therapy (24 weeks treatment duration if undetectable viremia at weeks 4 and 12) was 84% in 222 naïve/relapser F3 patients. Independent predictors of response were: (A) F3 (odds ratio (OR) = 1.51, 95% CI 1.31- 2.00, p = 0.005), (B) subtype 1b (OR = 1.63, 95% CI 1.18-2.24, p = 0.0029), (C) alpha-fetoprotein <10 ng/ml (OR = 2.50, 95% CI 1.87-3.36, p <0.0001) and (D) any prior response other than null (OR = 3.29, 95% CI 2.40-4.52, p <0.0001). SVR24 rose for patients who had more of these predictive factors: 6/32 (19%) for none, 38/139 (27%) for 1, 129/260 (50%) for 2, 202/329 (61%) for 3, and 194/235 (83%) for 4 factors. Grade 2-4 treatment-related adverse events (AE) were experienced by 719 (67%) patients; 169 (16%) discontinued therapy for AE and 7 (0.6%) died during the PR tail. Conclusions: Naïve and experienced patients with advanced fibrosis or cirrhosis d<br />SCOPUS: ar.j<br />info:eu-repo/semantics/published

Details

Database :
OAIster
Journal :
Journal of hepatology, 61 (5
Notes :
1 full-text file(s): application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.ocn922574335
Document Type :
Electronic Resource