As
reported in the August 2007 issue of Hepatology, researchers conducted
a study to determine whether using erythropoietin, or epoetin alpha (EPO), with
or without a higher dose of ribavirin, could enhance sustained
virological response (SVR) rates.
They
randomized 150 treatment-naive patients (36% African-American) with chronic genotype
1 hepatitis C into 3 treatment groups:
In
groups 2 and 3, EPO was started at the onset of therapy in order to maintain hemoglobin
levels between 12 and 15 g/dL. When required, the ribavirin dose was reduced by
200-mg steps.
Results
A significantly smaller percentage of patients in Group 2 compared with Group
1 had a decline in hemoglobin to less than 10 g/dL (9% vs 34%; P < 0.05).
Fewer patients in Group
2 required ribavirin dose reduction (10% vs 40%) compared with Group 1 patients
(P < 0.05).
Despite this, SVR rates
were not significantly different in Group 1 and Group 2 (19% vs 29%).
However, the SVR rate
was significantly greater (49%) in Group 3 (P < 0.05).
This resulted from
a significantly lower HCV relapse rate: 8% in Group 3 vs 38% in Groups 1 and 2
(P < 0.05).
Conclusion
"We
conclude that using EPO in all subjects at the initiation of pegylated interferon
and ribavirin treatment will not enhance SVR given the same starting dose of ribavirin,"
the researchers stated. "In contrast, a higher starting dose of ribavirin
was associated with a lower relapse rate and higher rate of SVR."
08/24/07
Reference ML
Shiffman, J Salvatore, S Hubbard, and others. Treatment of chronic hepatitis C
virus genotype 1 with peginterferon, ribavirin, and epoetin alpha. Hepatology
46(2): 371-379. August 2007.