Does the metabolite uracil arabinoside inhibit cytosine arabinoside (Ara-C) penetration into the cerebrospinal fluid during high-dose Ara-C therapy?

H C van Prooijen, P Muus, J M Roelofs, K Punt
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引用次数: 5

Abstract

A patient with acute leukaemia was treated with i.v. 2-h infusions of Ara-C at a dose of 3.0 g/m2 every 12 h. During 6 d of therapy the concentrations of the metabolite Ara-U in the CSF reached rather high levels of between 60 and 70 mumol/l from d 2-6 due to high levels of Ara-U in the plasma. The concentration of Ara-C in the CSF after the first infusion was 10.8 mumol/l. After repetitive doses on d 2-6 the drug concentrations increased from about 3 mumol/l just before infusion to about 8 mumol/l at the end of infusion, indicating inhibition of Ara-C influx into the CSF during prolonged treatment. We suggest that the high levels of Ara-U in the plasma interfere with Ara-C transport across the blood-brain barrier.

在大剂量阿拉糖糖治疗期间,代谢产物阿糖糖尿嘧啶是否抑制阿糖糖胞嘧啶(阿拉糖糖c)进入脑脊液?
一名急性白血病患者每12小时静脉注射剂量为3.0 g/m2的Ara-C治疗2小时。在治疗的第6天,由于血浆中Ara-U的高水平,脑脊液中代谢物Ara-U的浓度从第2-6天起达到60至70 μ mol/l之间的相当高的水平。第一次给药后脑脊液中Ara-C浓度为10.8 μ mol/l。在第2-6天重复给药后,药物浓度从注射前的约3 μ mol/l增加到注射结束时的约8 μ mol/l,表明在长期治疗期间抑制了Ara-C流入脑脊液。我们认为血浆中高水平的Ara-U干扰了Ara-C通过血脑屏障的运输。
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