Hepatitis C Articles



Factors That Predict a Rapid Virological Response at Week 4 and a Sustained Virological Response at Week 24

Approximately one third of hepatitis C virus (HCV) genotype 1 patients achieved a sustained virological response (SVR) after 24 weeks of treatment with peginterferon alfa-2a (Pegasys) plus ribavirin in a randomized, multinational trial.

In the present study, researchers aimed to identify factors associated with a rapid virological response (RVR) at week 4 (HCV RNA <50 IU/mL) and a SVR (HCV RNA <50 IU/mL at the end of follow-up) in these patients.

Stepwise multiple logistic regression analysis was used to explore the prognostic factors for a RVR and SVR in genotype 1 patients treated for 24 weeks.

Results

Fifty-one of 216 (24%) genotype 1 patients in the 24-week treatment groups had a RVR.

SVR rates were considerably higher in patients without a RVR (89% vs. 19%, respectively) were more likely to achieve a RVR than those with HCV RNA greater than 600,000 IU/mL.

HCV subtype (1b vs. 1a) was also independently associated with.

RVR and baseline HCV RNA less than 200,000 IU/mL were significant and independent predictors of SVR in patients treated for 24 weeks.

In conclusion, the authors write, “Patients infected with HCV genotype 1 and treated with peginterferon alfa-2a plus ribavirin sustained a RVR 24% of the time. This portends an 89% probability of a SVR after 24 weeks of treatment.”

05/09/06

Reference
D M Jensen, T R Morgan, P Marcellin and others. Early identification of HCV genotype 1 patients responding to 24 weeks peginterferon alfa-2a (40 kd)/ribavirin therapy. Hepatology 43(5): 954-960.


FDA-approved Monotherapies for HCV
Intron A
Roferon

Infergen

Pegasys

PEG-Intron

FDA-approved Combination Therapies for HCV
Pegasys + Copegus
PEG-Intron + Rebetol
Intron A + Rebetol
Roferon A + Ribavirin