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Virologic response rates of weight-based taribavirin versus ribavirin in treatment-naive patients with genotype 1 chronic hepatitis C.
Poordad, Fred; Lawitz, Eric; Shiffman, Mitchell L; Hassanein, Tarek; Muir, Andrew J; Bacon, Bruce R; Heise, Jamie; Halliman, Deanine; Chun, Eric; Hammond, Janet.
Afiliación
  • Poordad F; Hepatology and Liver Transplantation, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA. fred.poordad@cshs.org
Hepatology ; 52(4): 1208-15, 2010 Oct.
Article en En | MEDLINE | ID: mdl-20721883
ABSTRACT
UNLABELLED Ribavirin-induced hemolytic anemia can prompt dose reductions and lower sustained virologic response (SVR) rates in the treatment of patients with chronic hepatitis C. The study aimed to determine if weight-based dosing of taribavirin (TBV), an oral prodrug of ribavirin (RBV), demonstrated efficacy comparable to RBV while maintaining its previously demonstrated anemia advantage with fixed dose administration. A U.S. phase 2b randomized, open-label, active-controlled, parallel-group study was conducted in 278 treatment-naive patients infected with genotype 1 who were stratified by body weight and baseline viral load. Patients were randomized 1111 to receive TBV (20, 25, or 30 mg/kg/day) or RBV (800-1400 mg/day) with pegylated interferon alfa-2b for 48 weeks. The SVR rates in this difficult-to-cure patient demographics (mean age, 49 years; 61% male; 30% African American or Latino; high viral load; advanced fibrosis; and mean weight, 82 kg) were 28.4%, 24.3%, 20.6%, and 21.4% in the 20, 25, and 30 mg/kg TBV groups and the RBV group, respectively. There were no statistical differences in the efficacy analyses. Anemia rates were significantly lower (P < 0.05) in the 20 and 25 mg/kg/day TBV treatment groups (13.4% and 15.7%, respectively) compared to RBV (32.9%). The most common adverse events in all groups were fatigue, diarrhea, and insomnia. Diarrhea, reported in 38% of TBV patients versus 21% of RBV patients, was generally mild and not dose-limiting.

CONCLUSION:

All TBV doses demonstrated efficacy and tolerability comparable to that of RBV; however, the 25 mg/kg dose demonstrated the optimal balance of safety and efficacy. Anemia rates were significantly lower for TBV given at 20-25 mg/kg than RBV. These data suggest weight-based dosing with TBV provides a safe and effective treatment alternative to RBV for chronic hepatitis C. American Association for the Study of Liver Diseases.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ribavirina / Hepatitis C Crónica Tipo de estudio: Clinical_trials Idioma: En Revista: Hepatology Año: 2010 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ribavirina / Hepatitis C Crónica Tipo de estudio: Clinical_trials Idioma: En Revista: Hepatology Año: 2010 Tipo del documento: Article