Phase II evaluation of metoprine in patients with non-small-cell lung carcinoma.

Cancer clinical trials Pub Date : 1981-01-01
G R Lynch, R J Gralla, D P Kelsen, E S Casper, M B Stoopler, R B Golbey
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引用次数: 0

Abstract

A phase II study of metoprine in low dose and in high dose with citrovorum rescue was conducted in patients with non-small-cell lung carcinoma. There were no responses observed in the 36 patients studied, yielding a predicted true response rate of less than 9%. Thrombocytopenia was the dose-limiting toxicity of the low-dose regimen; there was also one episode of leukopenia and sepsis in this group. Although citrovorum rescue obviated hematologic toxicity in the high-dose regimen, mild to moderate neurological toxicity occurred at this dose. Metoprine does not appear to be a useful agent in non-small-cell lung carcinoma when used in the dose schedule employed in this study.

美托普林在非小细胞肺癌患者中的II期评价。
在非小细胞肺癌患者中进行了一项低剂量和高剂量的美托林与citrovorum抢救的II期研究。在研究的36例患者中没有观察到应答,因此预测的真实应答率低于9%。血小板减少是低剂量方案的剂量限制性毒性;该组还发生过一次白细胞减少和脓毒症。虽然在高剂量方案中,citrovorum可避免血液学毒性,但在高剂量方案中出现轻度至中度神经毒性。在本研究中使用的剂量表中,美托林似乎不是治疗非小细胞肺癌的有效药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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