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急性淋巴细胞白血病患儿口服甲氨蝶呤后血清水平不可预测。

Unpredictable serum levels after oral methotrexate in children with acute lymphoblastic leukaemia.

作者信息

Kearney P J, Light P A, Preece A, Mott M G

出版信息

Cancer Chemother Pharmacol. 1979;3(2):117-20. doi: 10.1007/BF00254982.

Abstract

Serum methotrexate levels were measured for 5 h after oral intake in 11 children with acute lymphoblastic leukaemia. The curves obtained with the child's regular dose of methotrexate varied widely, and were independent of the doses used. Peak levels were found in samples taken up to 3h after ingestion, and ranged from 300 to 1250 ng/ml. In the doses used, methotrexate toxicity was present in one of the eleven children, and was associated with a delayed peak and a high 5-h methotrexate level. Individual drug metabolism could be an important factor in the response to treatment, and needs to be evaluated in the assessment of protocols.

摘要

对11名急性淋巴细胞白血病患儿口服甲氨蝶呤后5小时内的血清甲氨蝶呤水平进行了测定。患儿常规剂量甲氨蝶呤所获得的曲线差异很大,且与所用剂量无关。在摄入后3小时内采集的样本中发现了峰值水平,范围为300至1250纳克/毫升。在所使用的剂量中,11名患儿中有1名出现了甲氨蝶呤毒性,且与峰值延迟和5小时甲氨蝶呤高水平有关。个体药物代谢可能是治疗反应中的一个重要因素,在方案评估中需要进行评估。

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