HIVandHepatitis.com Highlights from the
56th Annual AASLD Conference

 November 11 - 15, 2005 San Francisco, California

HIVandHepatitis.com
HOME Page

HOME   Hepatitis B Main Section   Hepatitis C Main Section   HIV and AIDS Main Section
56th AASLD
Main Page

Short-term Treatment Duration for HCV Genotypes 2 and 3 Patients

It is well known that HCV genotypes 2 and 3 patients have significantly higher sustained response rates (SVR) to treatment compared to genotypes 1 and 4 patients. Prior studies have also demonstrated that 12-14 weeks treatment is effective in genotype 2 or 3 HCV patients who become HCV undetectable after 4 weeks of therapy rapid virologic response (RVR) or “Super Responders (SR)”.

In this retrospective study, 2 data sets of patients from Italy and Norway were pooled with the objective of identifying predictors of sustained virological response (SVR), RVR and relapse after short term treatment (12-14 weeks or 24 weeks) with peginterferon alfa-2b (PegIntron) (1.0, n=281 or 1.5 μg/kg, n=122) plus ribavirin (800-1200 mg). Dosing depended on negative or positive HCV RNA at week 4.

The primary endpoint was undetectable HCV-RNA 24 weeks after therapy (SVR).

Results

SVR was obtained in 313/403 patients (78%).

SVR differed between cases with or without RVR (85% vs 62%), mild or bridging fibrosis/cirrhosis (82% vs 67%), absent/mild or moderate/severe steatosis (84% vs 72%), HCV-2 or -3 (81% vs 73%) low or high viremia (80% vs 67%).

RVR, mild fibrosis, and HCV-2 were independent predictors of SVR.

RVR was obtained in 274/403 (68%) patients, 163/242 (67%) HCV2, and 111/161 (69%) HCV-3.

Patients with RVR had, as compared to those without RVR, more frequently low grade steatosis (72% vs 64%), mild fibrosis (70% vs 63%, and high PegIFN dose (78% vs 64%).

RVR was independent of viral load.

absence of severe fibrosis independently predicted RVR.

In RVR patients, SVR was achieved in 85% of both HCV-2 and HCV-3.

Virologic relapse was observed in 29/274 RVR patients (10.6%), and was more frequently observed among those with low ALT levels (14% vs 5%), high viremia (14% vs 6%), and severe fibrosis (18% vs 8%).

Peg-IFN dose, steatosis and genotype were not associated with risk of relapse.

Severe fibrosis and low ALT were independent predictors of relapse.

In conclusion, the authors write, “In HCV-2 or -3, the HCV RNA status after 4 weeks of therapy may guide treatment duration. Short treatment duration is effective in both HCV-2 and -3 patients with RVR, but those with severe fibrosis are less likely to experience both RVR and SVR, and more frequently relapse off therapy.”

11/18/05

Reference
A Andriulli and others. SHORT-TERM TREATMENT DURATION FOR HCV-2 AND HCV-3 INFECTED PATIENTS WITH CHRONIC HEPATITIS. Abstract 1234. Abstracts of the annual meeting of the American Association for the Study of Liver Diseases (56th AASLD). November 11-15, 2005. San Francisco, CA.