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急性淋巴细胞白血病患儿中剂量甲氨蝶呤的处置情况

Disposition of intermediate-dose methotrexate in children with acute lymphocytic leukemia.

作者信息

Evans W E, Stewart C F, Hutson P R, Cairnes D A, Bowman W P, Yee G C, Crom W R

出版信息

Drug Intell Clin Pharm. 1982 Nov;16(11):839-42. doi: 10.1177/106002808201601105.

Abstract

Intermediate-dose methotrexate (MTX 200 mg/m2 iv in a bolus dose, followed by 800 mg/m2 iv, infused over 24 hours) is being used as a component of therapy for children with acute lymphocytic leukemia. To define the extent of interpatient variability in MTX disposition, with this dosage and schedule, the systemic clearance of MTX was measured in 69 children (total doses, 717; median, 10 doses per patient). The mean (+/- SD) systemic clearance was 91.6 (+/- 25.2) ml/min/m2 and ranged from 50-161 ml/min/m2. Renal clearance was measured in 16 of these patients and averaged 50.7 (+/- 14) ml/min/m2 during the MTX infusion (0-24 h), at which time mean systemic clearance was 8.7 (+/- 19) and nonrenal clearance was 31.1 (+/- 11.8) ml/min/m2. Measurement of 7-hydroxy-methotrexate in serum and urine was consistent with the substantial amount of nonrenal (metabolic) clearance observed in these patients. Cerebrospinal fluid MTX concentrations, measured at 24 hours, were 0.26 (+/- 0.1) microM when only the intravenous MTX was given and 1.08 (+/- 0.8) microM when an intrathecal dose (12 mg/m2) was also given at the start of the 24-hour infusion. This study establishes that there is substantial interpatient variability in MTX disposition in children and suggests a possible cause of variable patient response to MTX.

摘要

中等剂量甲氨蝶呤(MTX,200mg/m²静脉推注,随后800mg/m²静脉滴注,持续24小时)被用作急性淋巴细胞白血病患儿治疗方案的一部分。为确定采用此剂量和给药方案时患者间MTX处置的变异性程度,对69名儿童(共717次给药;中位数为每名患者10次给药)的MTX全身清除率进行了测量。平均(±标准差)全身清除率为91.6(±25.2)ml/min/m²,范围为50 - 161ml/min/m²。对其中16名患者测量了肾清除率,在MTX输注期间(0 - 24小时)平均为50.7(±14)ml/min/m²,此时平均全身清除率为8.7(±19),非肾清除率为31.1(±11.8)ml/min/m²。血清和尿液中7 - 羟基甲氨蝶呤的测量结果与这些患者中观察到的大量非肾(代谢)清除一致。在24小时时测量的脑脊液MTX浓度,仅给予静脉MTX时为0.26(±0.1)μM,在24小时输注开始时同时给予鞘内剂量(12mg/m²)时为1.08(±0.8)μM。本研究证实儿童MTX处置存在显著的患者间变异性,并提示了患者对MTX反应不同的可能原因。

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