University of Wisconsin, Madison, Wisconsin, USA.
Antimicrob Agents Chemother. 2013 Nov;57(11):5642-8. doi: 10.1128/AAC.01354-13. Epub 2013 Sep 3.
Pharmacodynamic (PD) studies with triazoles in the neutropenic murine disseminated candidiasis model have been performed extensively for Candida albicans. They have consistently shown that the pharmacodynamic index most closely correlated with efficacy is the ratio of the 24-h area under the concentration-time curve (AUC) to the MIC, and a target 24-h free-drug AUC/MIC ratio near 25 is associated with 50% of maximal microbiologic efficacy. We utilized this model to investigate the pharmacodynamics of isavuconazole. Isavuconazole pharmacokinetics were linear over the dose range studied. Oral-gastric doses of 640, 160, 40, and 10 mg of prodrug/kg of body weight produced peak levels of 0.51 to 25.4 mg/liter, an elimination half-life of 1 to 5 h, and an AUC from 0 h to infinity (AUC0-∞) of 0.9 to 287 mg · h/liter. The AUC/MIC ratio was the pharmacodynamic index that correlated best with efficacy (R(2), 0.84). Pharmacodynamic target studies were performed using 4 C. albicans isolates with both a 24-h and a 96-h treatment duration. The strains were chosen to include previously characterized fluconazole-resistant strains. The mean 50% effective doses (ED50) (expressed in mg/kg of body weight/12 h) and associated 24-h free-drug AUC/MIC ratios were 89.3 ± 46.7 and 67.7 ± 35 for the 24-h treatment and 59.6 ± 22 and 33.3 ± 25.5 for the 96-h treatment. These differences were not statistically significant. Pharmacodynamic targets for two non-albicans Candida species were also explored. The mean ED50 (expressed in mg/kg/12 h) and associated 24-h free-drug AUC/MIC ratios were 31.2 and 6.2 for Candida tropicalis (n = 1) and 50.5 and 1.6 for Candida glabrata (n = 2). These PD targets were significantly different from C. albicans targets (P, 0.04). Isavuconazole PD targets for C. albicans are similar to those observed in this model with other triazoles. However, the PD targets for non-albicans Candida species were more than 10-fold lower than those for C. albicans (P, 0.04). This difference is similar to the species-specific PD relationships for the echinocandins. The lower PD targets for these species in this model will be important to consider in the analysis of clinical trial data and during the development of susceptibility breakpoints.
已针对白色念珠菌在中性粒细胞减少的播散性念珠菌病啮齿动物模型中进行了广泛的三唑类药物药效学 (PD) 研究。这些研究一致表明,与疗效最密切相关的药效学指标是 24 小时浓度-时间曲线下面积 (AUC) 与 MIC 的比值,并且接近 25 的目标 24 小时游离药物 AUC/MIC 比值与最大微生物疗效的 50%相关。我们利用该模型研究了伊曲康唑的药效学。伊曲康唑的药代动力学在研究的剂量范围内呈线性。口服胃饲 640、160、40 和 10 mg 前药/kg 体重,可使峰浓度达到 0.51 至 25.4 mg/L,消除半衰期为 1 至 5 小时,0 至无穷时 AUC(AUC0-∞)为 0.9 至 287 mg·h/L。AUC/MIC 比值是与疗效相关性最好的药效学指标(R(2),0.84)。使用 4 株白色念珠菌分离株进行了 24 小时和 96 小时治疗持续时间的药效学目标研究。选择这些菌株包括先前已确定的氟康唑耐药菌株。50%有效剂量(ED50)的平均值(以 mg/kg 体重/12 h 表示)和相关的 24 小时游离药物 AUC/MIC 比值分别为 89.3 ± 46.7 和 67.7 ± 35,用于 24 小时治疗,59.6 ± 22 和 33.3 ± 25.5 用于 96 小时治疗。这些差异无统计学意义。还探讨了两种非白色念珠菌属的念珠菌的药效学目标。C.热带念珠菌(n = 1)的平均 ED50(以 mg/kg/12 h 表示)和相关的 24 小时游离药物 AUC/MIC 比值为 31.2 和 6.2,C.光滑念珠菌(n = 2)的平均 ED50(以 mg/kg/12 h 表示)和相关的 24 小时游离药物 AUC/MIC 比值为 50.5 和 1.6。这些 PD 目标与白色念珠菌目标有显著差异(P,0.04)。伊曲康唑对白色念珠菌的 PD 目标与该模型中其他三唑类药物观察到的目标相似。然而,非白色念珠菌的 PD 目标比白色念珠菌低 10 多倍(P,0.04)。这种差异类似于棘白菌素的种间 PD 关系。在该模型中,这些种的较低 PD 目标在分析临床试验数据和开发药敏折点时将非常重要。