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本文引用的文献

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[ON THE ACTIVATION OF CYCLOPHOSPHAMIDE IN VIVO AND IN VITRO].[关于环磷酰胺在体内和体外的活化作用]
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Intrasubject variation in children of ifosfamide pharmacokinetics and metabolism during repeated administration.
Cancer Chemother Pharmacol. 1996;38(2):147-54. doi: 10.1007/s002800050463.
3
Activation of the anti-cancer drug ifosphamide by rat liver microsomal P450 enzymes.大鼠肝脏微粒体P450酶对抗癌药物异环磷酰胺的激活作用。
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A randomised study of bolus vs continuous pump infusion of ifosfamide and doxorubicin with oral etoposide for small cell lung cancer.一项关于大剂量注射与持续泵注异环磷酰胺和多柔比星联合口服依托泊苷治疗小细胞肺癌的随机研究。
Br J Cancer. 1993 Jun;67(6):1385-90. doi: 10.1038/bjc.1993.256.
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Pharmacokinetics and metabolism of ifosfamide administered as a continuous infusion in children.
Cancer Res. 1993 Aug 15;53(16):3758-64.
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The analysis of ifosfamide and its metabolites (review).异环磷酰胺及其代谢物的分析(综述)
Anticancer Res. 1993 Sep-Oct;13(5A):1311-24.
7
Metabolism of ifosfamide during a 3 day infusion.异环磷酰胺在3天输注期间的代谢情况。
Br J Cancer. 1994 May;69(5):931-6. doi: 10.1038/bjc.1994.180.
8
Identification of the major human hepatic cytochrome P450 involved in activation and N-dechloroethylation of ifosfamide.参与异环磷酰胺活化和N-去氯乙基化的主要人肝细胞色素P450的鉴定。
Biochem Pharmacol. 1994 Mar 29;47(7):1157-63. doi: 10.1016/0006-2952(94)90387-5.
9
Competitive inhibition of human liver microsomal cytochrome P450 3A-dependent steroid 6 beta-hydroxylation activity by cyclophosphamide and ifosfamide in vitro.体外环磷酰胺和异环磷酰胺对人肝微粒体细胞色素P450 3A依赖性甾体6β-羟化活性的竞争性抑制作用。
J Pharmacol Exp Ther. 1994 Aug;270(2):645-9.
10
Ifosfamide clinical pharmacokinetics.异环磷酰胺的临床药代动力学。
Clin Pharmacokinet. 1994 Jun;26(6):439-56. doi: 10.2165/00003088-199426060-00003.

大剂量推注和静脉滴注异环磷酰胺时的药代动力学和代谢:一项随机交叉研究。

The pharmacokinetics and metabolism of ifosfamide during bolus and infusional administration: a randomized cross-over study.

作者信息

Singer J M, Hartley J M, Brennan C, Nicholson P W, Souhami R L

机构信息

Department of Oncology, University College, London, UK.

出版信息

Br J Cancer. 1998 Mar;77(6):978-84. doi: 10.1038/bjc.1998.161.

DOI:10.1038/bjc.1998.161
PMID:9528844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2150089/
Abstract

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.

摘要

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。