Singer J M, Hartley J M, Brennan C, Nicholson P W, Souhami R L
Department of Oncology, University College, London, UK.
Br J Cancer. 1998 Mar;77(6):978-84. doi: 10.1038/bjc.1998.161.
In a randomized cross-over trial, 11 patients received ifosfamide (IFOS) in 21-day cycles, which alternated between 3 g m(-2) x (2 or 3) days given as a 1-h bolus doses, or the same total dose as a continuous infusion. Patients who received four or more cycles also alternated between two cycles on dexamethasone 4 mg 8 hourly for 3 days starting 8 h before IFOS, and two cycles off dexamethasone. A total of 34 patient cycles were studied and serum and urinary levels of IFOS, 2 dechloroethylifosfamide (2DC), 3 dechloroethylifosfamide (3DC), carboxyifosfamide (CX) and isophosphoramide mustard (IPM) were measured by thin-layer chromatography. No significant differences could be detected in the areas under the curve (AUCs) of serum concentration, nor in the proportion of IFOS or its metabolites found in the urine. There was no significant effect of dexamethasone on IFOS metabolism. These results indicate that there is no identifiable pharmacokinetic basis for insistence on either bolus or infusional methods of IFOS administration.
在一项随机交叉试验中,11名患者接受异环磷酰胺(IFOS)治疗,给药周期为21天,两种给药方式交替进行,一种是3g/m²×(2或3)天,以1小时静脉推注给药,另一种是相同总剂量持续输注。接受四个或更多周期治疗的患者,在两个周期中也交替进行:一个周期在IFOS给药前8小时开始,给予地塞米松4mg,每8小时一次,共3天;另一个周期不使用地塞米松。共研究了34个患者周期,通过薄层色谱法测定血清和尿液中IFOS、2-去氯乙基异环磷酰胺(2DC)、3-去氯乙基异环磷酰胺(3DC)、羧基异环磷酰胺(CX)和异磷酰胺氮芥(IPM)的水平。血清浓度曲线下面积(AUCs)以及尿液中IFOS或其代谢产物的比例均未检测到显著差异。地塞米松对IFOS代谢没有显著影响。这些结果表明,坚持IFOS给药的推注或输注方法没有可识别的药代动力学依据。