Literature DB >> 17919233

Gamma-glutamyltransferase and rapid virological response as predictors of successful treatment with experimental or standard peginterferon-alpha-2b in chronic hepatitis C non-responders.

Jilling F Bergmann1, Jan M Vrolijk, Peter van der Schaar, Brigitte Vroom, Bart van Hoek, Annet van der Sluys Veer, Richard A de Vries, Elke Verhey, Bettina E Hansen, Johannes T Brouwer, Harry L A Janssen, Solko W Schalm, Robert J de Knegt.   

Abstract

BACKGROUND: High-dose peginterferon-alpha (PegIFN-alpha) induction and prolongation of therapy may be an option to improve sustained virological response (SVR) rates among hepatitis C virus (HCV) non-responders, although a higher and a longer dosing of PegIFN-alpha may intensify side effects.
METHODS: We randomized 53 patients, who previously failed with standard IFN-alpha+/-ribavirin, to a high-dose induction and an extended regimen with PegIFN-alpha-2b [3.0 microg/kg once weekly (q.w.) 12 weeks-->2.0 microg/kg q.w. 12 weeks-->1.5 microg/kg q.w. 48 weeks] or a standard regimen (1.5 microg/kg q.w. 48 weeks). All patients received daily weight-based ribavirin (800-1200 mg/day). The short-form 36 health survey was used to evaluate health-related quality of life (HRQL).
RESULTS: Intention-to-treat analysis showed no significant difference in SVR rate (44% vs. 37%, P=0.62) and relapse rate (9% vs. 31%, P=0.17) between experimental and standard treatment. Overall, 80% of the [positive predictive value (PPV)] patients with rapid virological response (RVR, HCV-RNA negativity at week 4) achieved SVR. No significant dose-related differences in HRQL were seen between both groups. At baseline, genotype 2 or 3 [odds ratio (OR): 7.4, 95% confidence interval (CI): 1.4-33.3, P=0.01] and gamma-glutamyltransferase (GGT) levels <2 x ULN (upper limit of normal) (OR: 6.76, 95% CI: 1.5-31.3, P=0.009) were significantly associated with SVR. Multivariate logistic regression at week 4 showed that only baseline GGT <2 x ULN (OR: 7.3, 95% CI: 1.4-38.5, P=0.01) and RVR (OR: 15.6, 95% CI: 3.2-76.9, P<0.001) were independently predictive for SVR.
CONCLUSION: Retreatment with PegIFN-alpha-2b and ribavirin for a minimum of 48 weeks should be considered in all patients unresponsive to previous IFN-based therapies. Baseline GGT values and RVR are highly predictive for retreatment outcome.

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Year:  2007        PMID: 17919233     DOI: 10.1111/j.1478-3231.2007.01540.x

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   5.828


  8 in total

1.  The determination of GGT is the most reliable predictor of nonresponsiveness to interferon-alpha based therapy in HCV type-1 infection.

Authors:  Viola Weich; Eva Herrmann; Tje Lin Chung; Christoph Sarrazin; Holger Hinrichsen; Peter Buggisch; Tilman Gerlach; Hartwig Klinker; Ulrich Spengler; Alexandra Bergk; Stefan Zeuzem; Thomas Berg
Journal:  J Gastroenterol       Date:  2011-09-13       Impact factor: 7.527

2.  Association of serum gamma-glutamyl transferase with treatment outcome in chronic hepatitis B patients.

Authors:  Rui Huang; Chen-Chen Yang; Yong Liu; Juan Xia; Ran Su; Ya-Li Xiong; Gui-Yang Wang; Zhen-Hua Sun; Xiao-Min Yan; Shan Lu; Chao Wu
Journal:  World J Gastroenterol       Date:  2015-09-14       Impact factor: 5.742

3.  Association of γ-glutamyl transferase (GGT) activity with treatment and clinical outcomes in chronic hepatitis C (HCV).

Authors:  James E Everhart; Elizabeth C Wright
Journal:  Hepatology       Date:  2013-04-05       Impact factor: 17.425

4.  Psychometric evaluation of the hepatitis C virus patient-reported outcomes (HCV-PRO) instrument: validity, responsiveness, and identification of the minimally important difference in a phase 2 clinical trial.

Authors:  Roger T Anderson; Robert W Baran; Pennifer Erickson; Dennis A Revicki; Birgitta Dietz; Katherine Gooch
Journal:  Qual Life Res       Date:  2013-09-14       Impact factor: 4.147

5.  Change in γ-glutamyl transpeptidase activity as a useful tool in identifying a group of patients with elevated risk of hepatocellular carcinoma development after DAA treatment of chronic hepatitis C.

Authors:  Dorota Orzechowska; Katarzyna Klimowicz; Anna Stępień; Tomasz Mikuła; Mariusz Sapuła; Alicja Wiercińska-Drapało
Journal:  Clin Exp Hepatol       Date:  2021-03-15

6.  Differences in clinical outcomes among hepatitis C genotype 1-infected patients treated with peginterferon alpha-2a or peginterferon alpha-2b plus ribavirin: a meta-analysis.

Authors:  Eric Druyts; Edward J Mills; Jean Nachega; Christopher O'Regan; Curtis L Cooper
Journal:  Clin Exp Gastroenterol       Date:  2012-02-14

7.  A lower serum gamma-glutamyltransferase level does not predict a sustained virological response in patients with chronic hepatitis C genotype 1.

Authors:  Fatih Güzelbulut; Mesut Sezikli; Züleyha Akkan Cetinkaya; Selvinaz Ozkara; Can Gönen; Ayşe Oya Kurdaş Ovünç
Journal:  Gut Liver       Date:  2012-11-13       Impact factor: 4.519

8.  A low serum γ-glutamyltransferase level predicts a sustained virological response in patients with chronic hepatitis C genotype 1.

Authors:  Umit Bilge Dogan; Mustafa Salih Akin; Serkan Yalaki
Journal:  Gut Liver       Date:  2014-01-13       Impact factor: 4.519

  8 in total

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