Fractionated administration of high-dose cyclophosphamide: influence on dose-dependent changes in pharmacokinetics and metabolism

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作者
Dagmar Busse
Friedrich W. Busch
Eberhard Schweizer
Frank Bohnenstengel
Michel Eichelbaum
Peter Fischer
Kurt Schumacher
Walter E. Aulitzky
Heyo K. Kroemer
机构
[1] Dr. Margarete Fischer-Bosch-Institut für Klinische Pharmakologie,
[2] Auerbachstrasse 112,undefined
[3] D-70376 Stuttgart,undefined
[4] Germany Tel.: +49-711-81013705,undefined
[5] Fax: +49-711-859295,undefined
[6] Robert-Bosch-Krankenhaus,undefined
[7] Zentrum für Innere Medizin,undefined
[8] Abteilung Hämatologie & Onkologie,undefined
[9] Auerbachstrasse 110,undefined
[10] D-70376 Stuttgart,undefined
[11] Germany,undefined
[12] Institut für Organische Chemie und Isotopenforschung,undefined
[13] Universität Stuttgart,undefined
[14] Pfaffenwaldring 55,undefined
[15] 70569 Stuttgart,undefined
[16] Germany,undefined
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Key words Cyclophosphamide; High dose; Pharmacokinetics; Application schedule;
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摘要
Purpose: The alkylating agent cyclophosphamide (CP) is a prodrug that is metabolized to both cytotoxic and inactive compounds. We have previously shown that following dose escalation from conventional-dose (CD) to high-dose (HD) levels; the fraction of the dose cleared by bioactivation is significantly decreased (66% versus 48.5%) in favor of inactivating elimination pathways when the HD is given as a single 1-h infusion. Based on the concept of bioactivating enzyme saturation with increasing doses, we investigated the influence of fractionated application of HD-CP on dose-dependent changes in metabolism. Patients and methods: Plasma concentrations of CP (measured by high-performance liquid chromatography, HPLC) and urinary concentrations of CP and its major metabolites (quantified by [31P]-nuclear magnetic resonance spectroscopy; [31P]-NMR spectroscopy), were determined in four patients with high-risk primary breast cancer who received adjuvant chemotherapy including both CD-CP (500 mg/m2 infused over 1 h) and split HD-CP (50 mg/kg infused over 1 h on each of 2 consecutive days (d): d1 and d2. Results: (Data are given as mean values for CD and d1/d2 of HD, respectively). Systemic clearance (CL) of CP was similar during CD and d1 of HD, but significantly increased on d2 of HD (CL: 83 and 78/115 ml/min; P < 0.01 for d1 versus d2). The latter was translated into an increase in formation CL of both active (+16.4 ml/min) and inactive metabolites (+17.6 ml/min) and reflects autoinduction of metabolism. As compared with CD-CP, no statistically significant decrease was observed in the relative contribution of bioactivation CL to overall CL during both days of HD (63% versus 57%/53%). Recovery of intact CP in 24-h urine corresponded to 24%, 29%, 22% of the dose (P < 0.05 for d1 versus d2 of HD). Conclusions: Following dose escalation of CP, dividing the high dose over 2 days instead of one single infusion may favorably impact the metabolism of CP in terms of bioactivation. In addition, on day 2 of a split regimen, renal elimination of CP is decreased, which implies that more drug is available for metabolism.
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页码:263 / 268
页数:5
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