Weight-based high- and low-dose ribavirin in combination with peginterferon α-2b therapy for genotype 2 chronic hepatitis C: A randomized trial

Aim:  The optimal ribavirin dose in the treatment of patients infected with hepatitis C virus (HCV) genotype 2 remains to be elucidated. We aimed to seek the optimal ribavirin dose required for this genotype in a randomized trial. Methods:  We compared the efficacy and tolerability of the 24‐week pe...

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Veröffentlicht in:Hepatology research 2012-04, Vol.42 (4), p.351-358
Hauptverfasser: Kagawa, Tatehiro, Kojima, Sei-ichiro, Shiraishi, Koichi, Takashimizu, Shinji, Nagata, Naruhiko, Shiozawa, Hirokazu, Nishizaki, Yasuhiro, Ikeda, Akihiko, Tei, Yoshihiro, Atsukawa, Kazuhiro, Kamochi, Jun-ichiro, Wasada, Mitsuru, Numata, Makoto, Arase, Yoshitaka, Hirose, Shunji, Yamada, Takuji, Hata, Yasuo, Watanabe, Norihito, Morizane, Toshio, Mine, Tetsuya
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Sprache:eng
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Zusammenfassung:Aim:  The optimal ribavirin dose in the treatment of patients infected with hepatitis C virus (HCV) genotype 2 remains to be elucidated. We aimed to seek the optimal ribavirin dose required for this genotype in a randomized trial. Methods:  We compared the efficacy and tolerability of the 24‐week peginterferon α‐2b (1.5 µg/kg/week) therapy in combination with a weight‐based higher dose (600–1000 mg) and lower dose (400–800 mg) of ribavirin for genotype 2 patients. Noninferior margin was set at 10%. Results:  A total of 120 patients were randomized to a higher‐dose or a lower‐dose group. Sustained virological response (SVR) by intention‐to‐treat analysis was achieved in 47/58 (81.0%, 90% confidential interval [CI]: 72.6–89.5) patients in the higher‐dose group and 41/60 (68.3%, 90% CI: 58.5–78.2) patients in the lower‐dose group (difference, −12.7%; 90% CI, −25.7 to 0.3). Relapse rates were 10% and 21.6% in the higher‐dose and the lower‐dose groups, respectively. Multiple logistic regression analysis showed that ribavirin dose/kg body weight was the only significant predictor of SVR (≥9.5 mg/kg per day vs
ISSN:1386-6346
1872-034X
DOI:10.1111/j.1872-034X.2011.00944.x