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大剂量口服甲氨蝶呤与氟尿嘧啶间隔24小时序贯使用:一项临床毒性研究。

Use of high-dose oral methotrexate sequenced at 24 hours with 5-FU: a clinical toxicity study.

作者信息

Benz C, Silverberg M, Cadman E

出版信息

Cancer Treat Rep. 1983 Mar;67(3):297-9.

PMID:6831477
Abstract

Twenty-three patients with advanced carcinoma were treated with 131 courses of high-dose oral methotrexate (MTX), sequenced at 24 hours with 5-FU iv and subsequent leucovorin rescue. The 30% incidence of toxicity was predominantly mild to moderate mucositis and myelosuppression. Trough and peak serum MTX levels demonstrated that micromolar concentrations were sustained greater than 24 hours. Toxicity correlated with shorter re-treatment intervals and not with serum MTX levels. This regimen can be safely and conveniently administered to an outpatient population and deserves further assessment in phase II trials.

摘要

23例晚期癌症患者接受了131个疗程的大剂量口服甲氨蝶呤(MTX)治疗,24小时后静脉注射5-氟尿嘧啶(5-FU)并随后进行亚叶酸钙解救。30%的毒性发生率主要为轻至中度黏膜炎和骨髓抑制。血清MTX谷值和峰值水平显示微摩尔浓度持续超过24小时。毒性与较短的再治疗间隔相关,而与血清MTX水平无关。该方案可安全、方便地应用于门诊患者,值得在II期试验中进一步评估。

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