Early prediction of response in interferon monotherapy and in interferon-ribavirin combination therapy for chronic hepatitis C: HCV RNA at 4 weeks versus ALT

1999 ◽  
Vol 30 (2) ◽  
pp. 192-198 ◽  
Author(s):  
Johannes T. Brouwer ◽  
Bettina E. Hansen ◽  
Hubert G.M. Niesters ◽  
Solko W. Schalm
2000 ◽  
Vol 95 (10) ◽  
pp. 2928-2935 ◽  
Author(s):  
Mitchell L. Shiffman ◽  
Charlotte M. Hofmann ◽  
Joubin Gabbay ◽  
Velimir A. Luketic ◽  
Richard K. Sterling ◽  
...  

2001 ◽  
Vol 15 (7) ◽  
pp. 953-958 ◽  
Author(s):  
V. Di Marco ◽  
A. Vaccaro ◽  
D. Ferraro ◽  
G. Alaimo ◽  
V. Rodolico ◽  
...  

1997 ◽  
Vol 11 (4) ◽  
pp. 294-297 ◽  
Author(s):  
Frank H Anderson ◽  
Lecheng Zeng ◽  
Eric M Yoshida ◽  
Natalie R Rock

Preliminary reports suggest that patients with interferon (IFN)-resistant chronic hepatitis C respond better to a combination of IFN-α and nonsteroidal anti-inflammatory drugs than to IFN alone. The efficacy of IFN combined with ketoprofen in the treatment of patients with IFN-resistant chronic hepatitis C was evaluated. Seventeen patients, nonresponsive after at least six months of treatment with IFN-α2b and subsequently treated with the combination of IFN-α2b plus ketoprofen for four months, were studied. Serum aminotransferases (alanine aminotransferase [ALT] and aspartate aminotransferase [AST]) and serum hepatitis C virus (HCV) RNA were analyzed before and throughout treatment. No patient normalized serum aminotransferases after combination therapy. There were no significant differences in mean serum ALT and AST levels before and after ketoprofen intervention. Serum HCV RNA became undetectable after treatment in only one patient, but was detectable again three months after treatment cessation. These results provide no convincing evidence that the combination of IFN-α2b with ketoprofen improves the response to IFN in patients nonresponsive to IFN alone.


Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 3219-3219
Author(s):  
Maria E. Mancuso ◽  
Elena Santagostino ◽  
Maria G. Rumi ◽  
Silvia Linari ◽  
Antonio Coppola ◽  
...  

Abstract Pegylated interferon (Peg-IFN) plus ribavirin is the standard treatment for patients with chronic hepatitis C. In a multicenter open trial, we assessed the efficacy and tolerability of this treatment in 78 HIV negative hemophiliacs (age: 20–64 years) with persistently high transaminase values. Sixty-four were naïve and 14 were relapsers to IFN monotherapy. Cirrhosis was clinically detected in 12 patients (15%). HCV genotype was 1 in 69%, 2a/c in 14%, 3a in 14% and 4 in 3%. Peg-IFN alpha-2b was given subcutaneously at doses of 1.5 mcg/Kg/week for 48 weeks in genotypes 1 and 4 and for 24 weeks in genotypes 2 and 3; oral ribavirin at 800–1200 mg/day based on body weight. Treatment was stopped in patients with polymerase chain reaction positive HCV-RNA at month 6. Results: 11 patients (14%) withdrew for side effects (4) or non-compliance (7). Neutropenia (<500 cells/mmc), decompensated diabetes, ALT flares, and vomiting not responding to antiemetic drugs were reasons for treatment discontinuation. The median fall in hemoglobin levels was 3.1 g/dL. Weight loss (38%), fatigue (33%) and cephalalgia (15%) were frequent side effects. Thirty-two patients (41%) required dose reduction of ribavirin (23, 29%) or Peg-IFN (20, 26%). At the end of the 6-month follow-up, sustained virological response (SVR) was achieved in 43 patients (55%): 40/64 naïve (63%) and 3/14 relapsers (21%, p = 0.007). Five patients (6%), all relapsers to IFN monotherapy, had a virological breakthrough during treatment and 4 (5%) relapsed during the post-treatment follow-up period. SVR was obtained in 86% genotypes 2/3 and 43% genotypes 1/4 (p = 0.001). Predictors of SVR were evaluated by univariate analysis in the 64 naïve patients. SVR was significantly associated with HCV infection type 2 and 3 (86% vs 50% in HCV type 1 and 4; p = 0.008), absence of cirrhosis (97.5% vs 75% in non-responders; p = 0.02) and higher pre-treatment serum ALT levels (111 vs 75 IU/L in non-responders; p = 0.02). SVR rates did not differ in relation to patient’s age, pretreatment HCV viremia, median disease duration and compliance to full-dose treatment. Conclusions: combination therapy with Peg-IFN plus ribavirin is the recommended therapeutic option for hemophiliacs with hepatitis C chronic infection. Relapsers to IFN monotherapy may benefit of re-treatment with Peg-IFN plus ribavirin achieving at least 20% SVR. Genotype 2 and 3 infection is the most significant predictor of SVR.


2006 ◽  
Vol 19 (5) ◽  
pp. 265-274
Author(s):  
Yousef S. Khader ◽  
Anmar Dweek ◽  
Ahmad Alkafajei ◽  
Atallah Z. Rabi'

This meta-analysis was conducted to assess the efficacy and safety of interferon and ribavirin combination therapy (CT) versus interferon monotherapy (IMT) in inducing sustained response in interferon-naïve, relapser, and nonresponder chronic hepatitis C patients. A literature search was performed using the MEDLINE database for clinical trials published in the period between 1995 and 2003. A total of 31 randomized trials and 7 nonrandomized trials comparing CT with interferon alone or comparing different dose regimens of CT were included in this meta-analysis. The primary outcome measure was sustained virological response. The summary estimate of the odds ratio was obtained using the random effect model. The study showed that sustained virological response rate was significantly higher in interferon-naïve, relapser, and nonrespondent chronic hepatitis C patients who were on CT compared to IMT (odds ratio = 3.23, 17.65, and 4.71, respectively). There was no statistically significant difference in virological and biochemical responses between different dose regimens of CT. Side effects, dose reduction, and treatment discontinuation rates were significantly higher in patients receiving CT compared with IMT. Treatment with interferon plus ribavirin has a significant benefit on the virological and biochemical response in patients with chronic hepatitis C irrespective to the previous treatment, and it should be considered the treatment of choice in naïve, relapser, and nonrespondent chronic hepatitis C patients.


2012 ◽  
Vol 140 (9-10) ◽  
pp. 612-618
Author(s):  
Dragan Delic ◽  
Nikola Mitrovic ◽  
Natasa Popovic ◽  
Aleksandar Urosevic ◽  
Ivana Pesic ◽  
...  

Introduction. Chronic hepatitis C virus (HCV) infection can progress to liver cirrhosis that causes bleeding from the gastrointestinal tract, liver failure and primary hepatocellular carcinoma. Use of standard therapeutic option consists of recombinant pegylated interferon alpha 2a/b with ribavirin in order to eradicate virus and prevent complications. Objective. The aim of investigation was to evaluate efficiency of combination therapy (pegylated interferon alpha 2a/b plus ribavirin) in patients with chronic HCV infection and to estimate predictive factors for successful treatment. Methods. A total of 387 patients with confirmed diagnosis of hepatitis C were evaluated (aged 18-65 years of both genders). Patients were treated with pegylated interferon alpha 2a/b and ribavirin according to a standard regimen lasting 24 or 48 weeks, dependent on virus genotype. Results. Negative HCV RNA (PCR assay) was recorded in 79.7% of patients at the end of treatment. Six months after completed therapy, negative HCV RNA, i.e. stained virologic response (SVR) was assessed in 70.5% of patients. Statistical summary of our results concerning SVR confirmed better efficiency of combination therapy for the following parameters compared to other investigated variables: age ?40 (84.3% vs. 59.l%; p<0.0005), absence of cirrhosis (75.6% vs. 58.3%; p=0.003), lack of genotype 1 (86.6% vs. 61.8%; p<0.0005), and in patients who received full doses of pegylated interferon alpha 2a (78.3% vs. 63.3%; p=0.002). Conclusion. Combination therapy of recombinant pegylated interferon alpha 2a with ribavirin leads to SVR in the majority of treated patients (70.5%). Successful treatment depends on a variety of host and virus factors.


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