Schuler U, Ehninger G, Wagner T
Medizinische Universitätsklinik Tübingen, Federal Republic of Germany.
Cancer Chemother Pharmacol. 1987;20(3):248-52. doi: 10.1007/BF00570495.
Blood levels of cyclophosphamide (CP) and activated metabolites were measured in 11 patients undergoing a 2- to 4-day conditioning chemotherapy for bone marrow transplantation. Urinary excretion of CP was determined in five patients. CP half-life decreased after pretreatment from an average of 7.1 h on the 1st day to 5.5 h on the 2nd day (P less than 0.005) and to 4.3 h on the 4th day (P less than 0.005). No characteristic changes in urinary excretion could be observed. At the same time the exposure to non-protein-bound activated metabolites increased from 10.5 to 19.5 and 26.0 nmol x h/ml respectively (P less than 0.005 and P less than 0.04). Thus, in contrast to in vitro and animal studies, no evidence for an inhibition of activating enzymes could be found. On the contrary, pretreatment seems to enhance the production of the cytotoxic metabolites. The possible explanation of these changes by enzyme induction and by the role of saturated protein binding sites is discussed. Exposure to active metabolites might be altered by dose splitting or even by a change in the duration of the infusion.
对11例接受2至4天骨髓移植预处理化疗的患者测定了环磷酰胺(CP)及其活性代谢产物的血药浓度。对其中5例患者测定了CP的尿排泄量。预处理后CP半衰期从第1天的平均7.1小时降至第2天的5.5小时(P<0.005),并在第4天降至4.3小时(P<0.005)。未观察到尿排泄的特征性变化。与此同时,非蛋白结合活性代谢产物的暴露量分别从10.5增加至19.5和26.0 nmol·h/ml(P<0.005和P<0.04)。因此,与体外和动物研究相反,未发现激活酶受抑制的证据。相反,预处理似乎增强了细胞毒性代谢产物的产生。讨论了通过酶诱导以及饱和蛋白结合位点的作用对这些变化的可能解释。活性代谢产物的暴露可能会因剂量分割甚至输注持续时间的改变而改变。