Hénin E, You B, VanCutsem E, Hoff P M, Cassidy J, Twelves C, Zuideveld K P, Sirzen F, Dartois C, Freyer G, Tod M, Girard P
Université de Lyon, Lyon, France.
Clin Pharmacol Ther. 2009 Apr;85(4):418-25. doi: 10.1038/clpt.2008.220. Epub 2008 Dec 10.
For the purpose of developing a longitudinal model to predict hand-and-foot syndrome (HFS) dynamics in patients receiving capecitabine, data from two large phase III studies were used. Of 595 patients in the capecitabine arms, 400 patients were randomly selected to build the model, and the other 195 were assigned for model validation. A score for risk of developing HFS was modeled using the proportional odds model, a sigmoidal maximum effect model driven by capecitabine accumulation as estimated through a kinetic-pharmacodynamic model and a Markov process. The lower the calculated creatinine clearance value at inclusion, the higher was the risk of HFS. Model validation was performed by visual and statistical predictive checks. The predictive dynamic model of HFS in patients receiving capecitabine allows the prediction of toxicity risk based on cumulative capecitabine dose and previous HFS grade. This dose-toxicity model will be useful in developing Bayesian individual treatment adaptations and may be of use in the clinic.
为了建立一个纵向模型来预测接受卡培他滨治疗的患者的手足综合征(HFS)动态变化,使用了两项大型III期研究的数据。在卡培他滨治疗组的595例患者中,随机选择400例患者建立模型,另外195例患者用于模型验证。使用比例优势模型建立HFS发生风险评分模型,该模型是一种由通过动力学-药效学模型和马尔可夫过程估计的卡培他滨蓄积驱动的S形最大效应模型。纳入时计算的肌酐清除率值越低,HFS风险越高。通过视觉和统计预测检查进行模型验证。接受卡培他滨治疗的患者的HFS预测动态模型能够根据卡培他滨累积剂量和既往HFS分级预测毒性风险。这种剂量-毒性模型将有助于开发贝叶斯个体化治疗方案,并且可能在临床中有用。