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YM881(制癌菌素斯替马兰)混悬液经肝动脉灌注的I期研究。YM881动脉内灌注治疗研究组

[Phase I study of YM881 (zinostatin stimalamer) suspension by hepatic arterial infusion. Research Group for Intra-arterial Infusion Therapy with YM881].

作者信息

Taguchi T, Saito T, Ota J, Nakao I, Ohashi K, Nakamura H, Konno T

机构信息

Dept. of Oncologic Surgery, Research Institute for Microbial Diseases, Osaka University, Suita, Japan.

出版信息

Gan To Kagaku Ryoho. 1991 Aug;18(10):1657-63.

PMID:1651686
Abstract

A phase I study of YM-881 (zinostatin stimalamer), neocarzinostatin combined with butylesterified styrene maleate, suspended in iodized poppy oil ethyl ester, was conducted in patients with hepatocellular carcinoma by giving single intra-arterial infusions via catheters inserted by Seldinger's method. Four dose levels, 2, 4, 6, and 8 mg, were tested. Major adverse reactions were fever, anorexia, nausea, vomiting, and abnormal hepatic function. Both the incidence and severity of adverse reactions tended to increase with the 8 mg dose. Tumor regression of 50% or more occurred in one receiving 2 mg and one receiving 4 mg. The results of the study suggest that doses of 6 mg or less may be appropriate for the phase II studies.

摘要

一项关于YM - 881(链黑菌素司他莫司)的I期研究开展,该药物是将新制癌菌素与丁酯化苯乙烯马来酸酯结合,并悬浮于碘化罂粟油乙酯中,通过经Seldinger法插入的导管对肝细胞癌患者进行单次动脉内输注给药。测试了四个剂量水平,即2毫克、4毫克、6毫克和8毫克。主要不良反应为发热、厌食、恶心、呕吐及肝功能异常。不良反应的发生率和严重程度均倾向于随8毫克剂量而增加。接受2毫克和4毫克剂量的各有一名患者出现50%或更高的肿瘤消退。该研究结果表明,6毫克或更低剂量可能适合II期研究。

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