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萘呋胺酯:针对人类恶性肿瘤活性的体外克隆形成评估

Nafazatrom: clonogenic in-vitro assessment of activity against human malignancies.

作者信息

Haas C D, Kyle G W, Crissman J D, Schaldenbrand M F

出版信息

Invest New Drugs. 1984;2(1):7-11. doi: 10.1007/BF00173781.

Abstract

Nafazatrom was tested against a variety of human malignancies with the human tumor stem cell assay at one or more of the following concentrations: 1, 10, 25, and 100 micrograms/ml X 1 h or 0.05, 0.5, or 5 micrograms/ml by continuous exposure. Major (greater than or equal to 70%) inhibition was noted in 7/52 adenocarcinomas, in 0/9 squamous carcinomas, and 1/17 other malignancies. Intermediate levels of inhibition (50 to 69%) were noted in 7/52, 4/9, and 6/17 of these respective subtypes. No clear trend toward superiority of any dose-schedule was noted. Since nafazatrom has proven non-toxic in our nearly completed Phase I study, and since this study suggests activity against several human cancers, Phase II level testing is warranted.

摘要

在人肿瘤干细胞试验中,以以下一种或多种浓度对萘呋胺酯进行了针对多种人类恶性肿瘤的测试:1、10、25和100微克/毫升×1小时,或通过持续暴露给予0.05、0.5或5微克/毫升。在52例腺癌中有7例、9例鳞状细胞癌中有0例、17例其他恶性肿瘤中有1例出现了主要(大于或等于70%)抑制。在这些相应亚型中,分别有7/52、4/9和6/17出现了中等程度的抑制(50%至69%)。未观察到任何剂量方案具有明显优势的趋势。由于萘呋胺酯在我们即将完成的I期研究中已证明无毒,且该研究表明其对多种人类癌症具有活性,因此有必要进行II期水平测试。

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