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首页> 外文期刊>Clinical Pharmacology and Therapeutics >Ribavirin dosing in chronic hepatitis C: Application of population pharmacokinetic-pharmacodynamic models.
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Ribavirin dosing in chronic hepatitis C: Application of population pharmacokinetic-pharmacodynamic models.

机译:利巴韦林在慢性丙型肝炎中的剂量:人群药代动力学-药效学模型的应用。

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BACKGROUND: Combination therapy of ribavirin with interferon alfa-2b and pegylated interferon alfa-2b is currently approved for the treatment of chronic hepatitis C. Approved ribavirin dosages vary from a fixed dosage of 800 mg/d to as much as 1200 mg/d on the basis of body weight. OBJECTIVE: Our objective was to evaluate ribavirin dosing strategies by comparison of their relative efficacy and toxicity profiles. METHODS: Three models were developed on the basis of data collected from a large phase III trial. A population pharmacokinetic model was used to describe the ribavirin dose-concentration relationship and the influence of covariates. Logistic regression models were developed for both sustained virologic response and hematologic toxicity. Ribavirin concentration was an important explanatory variable for both response and toxicity. Simulations of these models were developed for different ribavirin doses to obtain efficacy and toxicity profiles across the various dosing strategies. These strategies included a fixed 800-mg/d dose, empiric weight-adjusted doses (ie, 1000 mg/d for patients who weighed 75 kg [1000/1200 mg/d on the basis of body weights 75 kg] and 800 mg/d for patients who weighed <65 kg, 1000 mg/d for patients who weighed from 65 to 85 kg, and 1200 mg/d for patients who weighed >85 kg [800/1000/1200 mg/d on the basis of body weights <65/65-85/>85 kg]), a dose of 13 mg/kg per day, and other per-body weight doses between 9 and 16 mg/kg per day. RESULTS: Simulation results showed that both efficacy and toxicity increased as the milligrams-per-kilogram dose of ribavirin increased. The body weight-based 800/1000/1200-mg/d dose had overall response and toxicity rates that were 6.3% and 2.5% higher than those of the fixed 800-mg/d dose. In particular, patients with genotype-1 disease had a 7.4% increase in response rate. There were no differences in response and toxicity rates between the 800/1000/1200-mg/d and 13-mg/kg per day dose groups. CONCLUSIONS: This simulation suggests that ribavirin dosage (in combination with pegylated interferon alfa-2b) for patients with chronic hepatitis C should be based on body weight.
机译:背景:利巴韦林与干扰素α-2b和聚乙二醇化干扰素α-2b的联合治疗目前已被批准用于治疗慢性丙型肝炎。利巴韦林的批准剂量范围从固定剂量800毫克/天到1200毫克/天不等。体重的基础。目的:我们的目的是通过比较利巴韦林的相对疗效和毒性概况来评估利巴韦林的给药策略。方法:根据从大型III期试验收集的数据开发了三种模型。群体药代动力学模型用于描述利巴韦林的剂量-浓度关系和协变量的影响。为持续的病毒学应答和血液学毒性开发了逻辑回归模型。利巴韦林浓度是反应和毒性的重要解释变量。针对不同的利巴韦林剂量开发了这些模型的仿真,以在各种给药策略中获得功效和毒性概况。这些策略包括固定的800 mg / d剂量,经验性的体重调整剂量(即,对于≤75 kg的患者为10​​00 mg / d,对于大于75 kg的患者为1200 mg / d [1000/1200 mg / d(基于体重 75 kg],体重<65 kg的患者为800 mg / d,体重65至85 kg的患者为10​​00 mg / d,体重> 85千克[以体重<65 / 65-85 /> 85千克为基础的800/1000/1200毫克/天],每天13毫克/千克的剂量以及其他每体重的患者剂量介于每天9到16 mg / kg之间。结果:模拟结果表明,随着病毒唑每公斤毫克剂量的增加,功效和毒性均增加。基于体重的800/1000 / 1200-mg / d剂量的总反应和毒性率比固定的800-mg / d分别高6.3%和2.5%。特别是,患有基因型1疾病的患者的缓解率提高了7.4%。每天800/1000 / 1200-mg / d和13-mg / kg剂量组之间的应答和毒性率无差异。结论:该模拟表明对于慢性丙型肝炎患者,利巴韦林的剂量(与聚乙二醇化干扰素α-2b联合使用)应基于体重。

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