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别嘌醇对间歇性大剂量推注5-氟尿嘧啶毒性的影响。

Effect of allopurinol on the toxicity of high-dose 5-fluorouracil administered by intermittent bolus injection.

作者信息

Howell S B, Pfeifle C E, Wung W E

出版信息

Cancer. 1983 Jan 15;51(2):220-5. doi: 10.1002/1097-0142(19830115)51:2<220::aid-cncr2820510209>3.0.co;2-w.

Abstract

The effect of allopurinol pretreatment on the toxicity of 5-fluorouracil (5-FU) was examined in a clinical trial. Twenty-three patients were given bolus infusions of 5-FU every two weeks in doses that produced mild toxicity (0.8-1.9 g/m2). On alternate courses patients were pretreated with allopurinol either 300 mg two hours prior to and 10 hours after 5-FU, or 300 mg every 8 hours for 4 doses starting 24 hours before 5-FU. Seventeen and 20 pairs of courses were evaluable from the 2- and 24-hour pretreatment groups, respectively. Allopurinol did not produce a significant degree of protection against 5-FU-induced myelosuppression or mucositis on either dose schedule. Neurotoxicity manifesting as both cerebellar and encephalopathic signs and symptoms was the most important toxicity encountered and was dose-limiting for 5-FU on this schedule. Mean oxipurinol serum concentrations at the time of 5-FU administration were 24 microM and 104 microM for the 2- and 24-hour allopurinol pretreatment schedules respectively. Allopurinol increased the T 1/2 of 5-FU by a mean of 67% in three of the four patients studied. Pretreatment with allopurinol did not reduce the toxicity of 5-FU administered as an intravenous bolus.

摘要

在一项临床试验中,研究了别嘌醇预处理对5-氟尿嘧啶(5-FU)毒性的影响。23例患者每两周接受一次5-FU大剂量静脉输注,剂量为产生轻度毒性的剂量(0.8-1.9 g/m²)。在交替疗程中,患者在5-FU给药前2小时及给药后10小时接受300 mg别嘌醇预处理,或在5-FU给药前24小时开始每8小时服用300 mg,共4剂。分别从2小时和24小时预处理组获得了17对和20对可评估疗程。两种给药方案下,别嘌醇均未对5-FU诱导的骨髓抑制或粘膜炎产生显著程度的保护作用。表现为小脑和脑病体征及症状的神经毒性是所遇到的最重要的毒性,并且是该给药方案下5-FU的剂量限制性毒性。在5-FU给药时,2小时和24小时别嘌醇预处理方案的平均氧嘌呤醇血清浓度分别为24 μM和104 μM。在所研究的4例患者中的3例中,别嘌醇使5-FU的T1/2平均增加了67%。别嘌醇预处理并未降低静脉推注5-FU的毒性。

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