van Warmerdam L J, Rodenhuis S, van Tellingen O, Maes R A, Beijnen J H
Department of Medical Oncology, Antoni van Leeuwenhoek Hospital/Netherlands Cancer Institute, Amsterdam.
Cancer Chemother Pharmacol. 1994;35(2):179-81. doi: 10.1007/BF00686644.
A limited sampling model for the estimation of the carboplatin area under the concentration versus time curve (AUC), as developed by Sørensen et al., was validated prospectively for the use in a high-dose combination chemotherapy schedule. The model allows an estimation of the AUC on the basis of only one timed plasma drug concentration, sampled at exactly 2.75 h after a 1-h carboplatin infusion. Pharmacokinetic curves were obtained from nine patients receiving carboplatin (400 mg/m2 per day) combined with cyclophosphamide (1500 mg/m2 per day), thiotepa (120 mg/m2 per day), and mesna (3 g/day) for 4 consecutive days. Peripheral blood stem-cell transplantation (PBSCT) was performed 3 days later to restore hematopoiesis. Using this combination of high doses, the model proved to be unbiased (MPE -3.40%; SE, 1.22%) and highly precise [root mean squared prediction error (RMSE), 5.15%; SE, 0.17%] for estimation of the AUC during 4 consecutive days. The validated limited sampling model provides a starting point for future pharmacokinetic studies in a larger population of patients, which might lead to more insight into the relationships with the pharmacodynamic outcome of carboplatin and may help in achieving more rational dosing of patients on the basis of an AUC determination.
由索伦森等人开发的用于估算卡铂浓度-时间曲线下面积(AUC)的有限采样模型,在高剂量联合化疗方案中的应用得到了前瞻性验证。该模型仅根据一次定时血浆药物浓度即可估算AUC,该浓度在1小时卡铂输注后恰好2.75小时采集。从9名接受卡铂(每天400mg/m²)联合环磷酰胺(每天1500mg/m²)、噻替派(每天120mg/m²)和美司钠(每天3g)连续4天治疗的患者中获得药代动力学曲线。3天后进行外周血干细胞移植(PBSCT)以恢复造血功能。使用这种高剂量组合,该模型在连续4天估算AUC时被证明是无偏的(平均预测误差-3.40%;标准误,1.22%)且高度精确[均方根预测误差(RMSE),5.15%;标准误,0.17%]。经过验证的有限采样模型为未来在更多患者群体中进行药代动力学研究提供了一个起点,这可能会更深入地了解与卡铂药效学结果的关系,并可能有助于在AUC测定的基础上实现更合理的患者给药。