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癌症患者中短时间和长时间静脉输注异环磷酰胺的药代动力学。

The pharmacokinetics of ifosfamide given as short and long intravenous infusions in cancer patients.

作者信息

Lewis L D, Fitzgerald D L, Mohan P, Thatcher N, Harper P G, Rogers H J

机构信息

Division of Clinical Pharmacology, United Medical School, Guy's Hospital, London.

出版信息

Br J Clin Pharmacol. 1991 Jan;31(1):77-82. doi: 10.1111/j.1365-2125.1991.tb03860.x.

Abstract
  1. We investigated the pharmacokinetics of ifosfamide 5 g m-2 given by two regimens. Six patients (one female), median age 55 (range 40-71) years, all with lung cancer received 5 g m-2 ifosfamide (median ifosfamide dose 8.95 g) as an intravenous infusion over 0.5 h with mesna. Four other cancer patients (all male) of median age 52.5 (range 23-72) years were studied on seven treatment occasions with 5 g m-2 ifosfamide (median ifosfamide dose 8.88 g) as a 24 h intravenous infusion with mesna. Plasma was assayed for ifosfamide by gas liquid chromatography and for alkylating activity by the nitrobenzylpyridine method. 2. After ifosfamide 5 g m-2 infused over 0.5 h, the decay of the plasma ifosfamide concentration was monoexponential with a median (range) t1/2,z of 5.4 h (3.6-10.4 h). The median clearance was 60 ml min-1 (47-104) and the median volume of distribution was 388 (329-783) ml kg-1. Plasma nitrobenzylpyridine alkylating activity showed a biexponential decay in four patients and a monoexponential decay in two, with a median AUC of 102 (24-177) nmol nor nitrogen mustard eq h ml-1. 3. When ifosfamide 5 g m-2 was given as a 24 h infusion, the decay of the plasma ifosfamide concentration was monoexponential, the median (range) t1/2,z was 4.5 (3.4-6.1), the median volume of distribution was 563 (292-818) ml kg-1 and the median clearance was 79 (59-116) ml min-1. Plasma nitrobenzylpyridine alkylating activity decayed monoexponentially and the median AUC was 49 (45-131) nmol nor nitrogen mustard eq ml-1 h.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 我们研究了两种给药方案给予5 g/m²异环磷酰胺的药代动力学。6例患者(1例女性),中位年龄55岁(范围40 - 71岁),均为肺癌患者,接受5 g/m²异环磷酰胺(中位异环磷酰胺剂量8.95 g)静脉输注0.5小时,并同时给予美司钠。另外4例癌症患者(均为男性),中位年龄52.5岁(范围23 - 72岁),在7个治疗周期中接受5 g/m²异环磷酰胺(中位异环磷酰胺剂量8.88 g)24小时静脉输注,并同时给予美司钠。采用气相色谱法测定血浆中的异环磷酰胺,采用硝基苄吡啶法测定烷基化活性。2. 5 g/m²异环磷酰胺经0.5小时输注后,血浆异环磷酰胺浓度呈单指数衰减,中位(范围)t1/2,z为5.4小时(3.6 - 10.4小时)。中位清除率为60 ml/min(47 - 104),中位分布容积为388(329 - 783)ml/kg。4例患者血浆硝基苄吡啶烷基化活性呈双指数衰减,2例呈单指数衰减,中位AUC为102(24 - 177)nmol/氮芥当量·小时·ml⁻¹。3. 当5 g/m²异环磷酰胺采用24小时输注时,血浆异环磷酰胺浓度呈单指数衰减,中位(范围)t1/2,z为4.5(3.4 - 6.1),中位分布容积为563(292 - 818)ml/kg,中位清除率为79(59 - 116)ml/min。血浆硝基苄吡啶烷基化活性呈单指数衰减,中位AUC为49(45 - 131)nmol/氮芥当量·ml⁻¹·小时。(摘要截选至250字)

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