Aviles P, Falcoz C, San Roman R, Gargallo-Viola D
Glaxo Wellcome S.A., Parque Tecnológico de Madrid, Spain.
Antimicrob Agents Chemother. 2000 Sep;44(9):2333-40. doi: 10.1128/AAC.44.9.2333-2340.2000.
Sordarins are a new class of antifungal agents which selectively inhibit fungal protein synthesis (FPS) by impairing the function of elongation factor 2. The present study investigates possible correlations between sordarin pharmacokinetic (PK) properties and therapeutic efficacy, based on a murine model of invasive systemic candidiasis, and provides a rationale for dose selection in the first study of efficacy in humans. A significant correlation between PK parameters and the in vivo activity of GM 237354, taken as a representative FPS inhibitor, was demonstrated in a murine model of lethal systemic candidiasis. Area under the concentration-time curve (AUC) and maximum concentration of drug in serum (C(max)) over 24 h were determined after a single GM 237354 subcutaneous (s.c.) dose (50 mg/kg of body weight) in healthy animals (no significant PK changes with infection were observed for other sordarin derivatives). These results have been used to simulate PK profiles obtained after several doses and/or schedules in animal therapy. A PK-pharmacodynamic (PD) parameter such as the time that serum drug concentrations remain above the MIC (t > MIC) was also determined. Treatment efficacies were evaluated in terms of the area under the survival time curve (AUSTC), using Kaplan-Meier survival analysis and in terms of kidney fungal burden (log CFU/gram) after s.c. doses of 2.5, 5, 10, 20, and 40 mg/kg every 4, 8, or 12 h (corresponding to total daily doses of 5 to 240 mg/kg). The results show all treatments to significantly prolong survival versus that of infected and nontreated controls (P < 0.05). Relationships between simulated PK and PK-PD parameters and efficacy were explored. A good correlation independent of the dosing interval was observed with AUC (but not C(max) or t > MIC) and both AUSTC and kidney burden. Following repeated dosing every 8 h, AUC(50) (AUC at which 50% of the maximum therapeutic efficacy is obtained) was estimated as 21.7 and 37.1 microg. h/ml (total concentrations) for AUSTC and kidney burden using a sigmoid E(max) and an inhibitory sigmoid E(max) PK-PD model, respectively. For an efficacy target of 90% survival, AUC was predicted as 67 microg. h/ml. We conclude that the PK-PD approach is useful for evaluating relationships between PK parameters and efficacy in antifungal research. Moreover, the results obtained with this approach could be successfully applied to clinical studies.
梭链孢菌素是一类新型抗真菌药物,通过损害延伸因子2的功能来选择性抑制真菌蛋白质合成(FPS)。本研究基于侵袭性系统性念珠菌病小鼠模型,探讨梭链孢菌素药代动力学(PK)特性与治疗效果之间可能的相关性,并为人类首次疗效研究中的剂量选择提供依据。在致死性系统性念珠菌病小鼠模型中,已证明作为代表性FPS抑制剂的GM 237354的PK参数与体内活性之间存在显著相关性。在健康动物中单次皮下(s.c.)注射GM 237354(50 mg/kg体重)后,测定24小时内的血药浓度-时间曲线下面积(AUC)和血清中药物的最大浓度(C(max))(未观察到其他梭链孢菌素衍生物因感染而出现显著的PK变化)。这些结果已用于模拟动物治疗中多次给药和/或给药方案后的PK曲线。还确定了一个PK-药效学(PD)参数,如血清药物浓度保持高于MIC的时间(t > MIC)。使用Kaplan-Meier生存分析,根据生存时间曲线下面积(AUSTC)评估治疗效果,并根据每4、8或12小时皮下注射2.5、5、10、20和40 mg/kg剂量(相当于每日总剂量5至240 mg/kg)后的肾脏真菌负荷(log CFU/克)进行评估。结果显示,与感染且未治疗的对照组相比,所有治疗均显著延长了生存期(P < 0.05)。探讨了模拟PK和PK-PD参数与疗效之间的关系。观察到AUC(而非C(max)或t > MIC)与AUSTC和肾脏负荷之间存在良好的相关性,且与给药间隔无关。每8小时重复给药后,使用S型E(max)和抑制性S型E(max) PK-PD模型分别估计AUSTC和肾脏负荷的AUC(50)(获得最大治疗效果的50%时的AUC)为21.7和37.1 μg·h/ml(总浓度)。对于90%生存率的疗效目标,预测AUC为67 μg·h/ml。我们得出结论,PK-PD方法有助于评估抗真菌研究中PK参数与疗效之间的关系。此外,用该方法获得的结果可成功应用于临床研究。