Bruno R, Iliadis A, Favre R, Lena N, Imbert A M, Cano J P
Cancer Drug Deliv. 1985 Fall;2(4):277-83. doi: 10.1089/cdd.1985.2.277.
Population pharmacokinetics of methotrexate (MTX) was evaluated from intravenous test-dose (TD) data (n = 20 corresponding to 174 measured samples). Bayesian prediction of MTX clearance from TD experiments combining population data with measured levels (at times 0.5 and 6 h) was found to be feasible in routine situations with good performance (root mean squared error : rmse (precision) = 1.14 1.h-1 (11.2%) and mean error : me (bias) = 0.06 1.h-1 (NS) relatively to weighted least-square estimates, n = 50). The precision of Bayesian prediction was comparable to that of the model independent which is used in routine practice and involves 9 measured levels over 30 h, (rmse = 1.35 1.h-1 (10.9%), n = 50). However, the routine method presented a significative bias (me = -0.81 1.h-1, n = 50).
从静脉注射试验剂量(TD)数据(n = 20,对应174个测量样本)评估了甲氨蝶呤(MTX)的群体药代动力学。发现在常规情况下,将群体数据与测量水平(在0.5小时和6小时)相结合,通过TD实验对MTX清除率进行贝叶斯预测是可行的,且性能良好(均方根误差:rmse(精密度)= 1.14 l·h⁻¹(11.2%),平均误差:me(偏差)= 0.06 l·h⁻¹(无显著性差异),相对于加权最小二乘法估计值,n = 50)。贝叶斯预测的精密度与常规实践中使用的独立模型相当,该独立模型在30小时内涉及9个测量水平(rmse = 1.35 l·h⁻¹(10.9%),n = 50)。然而,常规方法存在显著偏差(me = -0.81 l·h⁻¹,n = 50)。