Moore M J, Erlichman C, Thiessen J J, Bunting P S, Hardy R, Kerr I, Soldin S
Department of Medicine, Princess Margaret Hospital, University of Toronto, Ontario, Canada.
Cancer Chemother Pharmacol. 1994;33(6):472-6. doi: 10.1007/BF00686503.
A total of 23 women with stage II breast cancer receiving adjuvant cyclophosphamide, methotrexate and 5-fluorouracil had detailed pharmacokinetic monitoring performed on the first and third courses of therapy. The area under the concentration time curve (AUC) of each of these three drugs varied by a factor of 3-4 among patients. No systematic change in pharmacokinetics between the first and third courses was seen for cyclophosphamide, methotrexate or 5-fluorouracil, and the mean AUC for each of the three drugs did not change. However, significant intrapatient variability in drug pharmacokinetics was observed for all three drugs such that the AUC, clearance and half-life in an individual on the third course could not be reliably predicted from data generated on the first course. On the basis of these results, cyclophosphamide, methotrexate, and 5-fluorouracil pharmacokinetic data from one treatment would not be useful information from which the doses of subsequent courses could be determined.
共有23名接受辅助性环磷酰胺、甲氨蝶呤和5-氟尿嘧啶治疗的II期乳腺癌女性患者在治疗的第一疗程和第三疗程进行了详细的药代动力学监测。这三种药物中每种药物的浓度-时间曲线下面积(AUC)在患者之间相差3至4倍。环磷酰胺、甲氨蝶呤或5-氟尿嘧啶在第一疗程和第三疗程之间未观察到药代动力学的系统性变化,且这三种药物各自的平均AUC没有改变。然而,所有三种药物均观察到显著的患者内药代动力学变异性,以至于无法根据第一疗程产生的数据可靠地预测个体在第三疗程时的AUC、清除率和半衰期。基于这些结果,来自一个疗程的环磷酰胺、甲氨蝶呤和5-氟尿嘧啶药代动力学数据对于确定后续疗程的剂量而言并非有用信息。