Literature DB >> 17410285

Efficacy, tolerability and predictive factors for early and sustained virologic response in patients treated with weight-based dosing regimen of PegIFN alpha-2b ribavirin in real-life healthcare setting.

Liana Gheorghe1, Speranta Iacob, Ioan Sporea, Mircea Grigorescu, Roxana Sirli, Dana Damian, Cristian Gheorghe, Razvan Iacob.   

Abstract

BACKGROUND AND AIM: Increasing evidence to date highlights that individualized treatment regimens with pegylated interferon (PegIFN) and ribavirin represent a better approach for patients nowadays showing negative predictive factors for sustained virological response. The aims of this study were to assess the rate of early (EVR) and sustained virological response (SVR), tolerability and baseline predictive factors associated with EVR and SVR in patients with chronic hepatitis C treated with individualized weight-based dosing regimen for both PegIFN alpha-2b and ribavirin.
METHODS: The observational analysis included 234 consecutive patients with chronic hepatitis C genotype 1 treated with PegIFN alpha-2b and ribavirin on an out-patient basis between January 2003-March 2006.
RESULTS: The mean age of the study group was 49.5 years, and 35% were male patients; the group was slightly overweight (mean BMI=26.5 kg/sq.m). EVR was achieved in 84.6% (198/234 patients). The end-of-treatment and sustained biochemical responses were 76.3% and 66.1%, respectively. At the end of follow-up, an overall intent-to-treat SVR was achieved by 71 of 127 patients (in 55.9%). Lower baseline (< 1,000 000 IU/mL) HCV viral load was the only predictive factor associated with EVR (p=0.04); absent or mild fibrosis (F0-1) and a low histological activity (HAI < 8) were independently associated with SVR. Side effects resulted in PegIFN and ribavirin dose reductions in 9.4% and, respectively, 18.1%, but definitive discontinuation of therapy was necessary only in 8.7% of patients.
CONCLUSION: PegIFN alpha-2b and ribavirin can be safe and successful when using a weight-based dosing regimen, leading to high response rates even in overweight patients.

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Year:  2007        PMID: 17410285     DOI: 10.1007/s11749-007-0047-9

Source DB:  PubMed          Journal:  J Gastrointestin Liver Dis        ISSN: 1841-8724            Impact factor:   2.008


  9 in total

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6.  Interleukin-28B (rs12979860) gene variation and treatment outcome after peginterferon plus ribavirin therapy in patients with genotype 1 of hepatitis C virus.

Authors:  Hamid Kalantari; Tahmine Tavakoli; Bahram Bagherpour; Shahram Honarmand
Journal:  J Res Med Sci       Date:  2014-11       Impact factor: 1.852

7.  The interleukin 28B gene polymorphism, rs8099917, in patients with chronic hepatitis C and response to the treatment with pegylated interferon and ribavirin.

Authors:  Hamid Kalantari; Bahram Bagherpour; Tahmine Tavakoli; Mahsa Khodadoostan; Seyed Mehdi Hejazi; Alireza Saadatmand
Journal:  J Res Med Sci       Date:  2019-02-25       Impact factor: 1.852

8.  Factors associated with rapid and early virologic response to peginterferon alfa-2a/ribavirin treatment in HCV genotype 1 patients representative of the general chronic hepatitis C population.

Authors:  M Rodriguez-Torres; M S Sulkowski; R T Chung; F M Hamzeh; D M Jensen
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9.  Weight loss, leukopenia and thrombocytopenia associated with sustained virologic response to Hepatitis C treatment.

Authors:  Nuntra Suwantarat; Alan D Tice; Thana Khawcharoenporn; Dominic C Chow
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  9 in total

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