Kanzawa F, Matsushima Y, Chiang C D, Nakano H, Nakagawa K, Takahashi H, Morinaga S, Tsuchiya R, Sasaki Y, Eguchi K
Pharmacology Division, National Cancer Center Research Institute, Tokyo, Japan.
Invest New Drugs. 1987 Dec;5(4):339-43. doi: 10.1007/BF00169972.
We have utilized a human tumor clonogenic assay (HTCA), as a disease-oriented drug screening model of new antitumor drugs, to test the antitumor activity of FR66973 and compared the activity with that of its analogous compound, mitomycin C. The overall in vitro response rate (defined as less than 50% survival of tumor colony forming units) for FR66973 against fresh tumor cells obtained from patients with non-small cell lung carcinoma (NSCLC) was 32%, 50% and 89% at 0.1, 1 and 10 micrograms/ml, respectively, which was superior to that of mitomycin C at the corresponding concentration. Our data suggest that FR66973 is a promising new drug against NSCLC. If phase I toxicities are not prohibitive, FR66973 may also have good activity against NSCLC in clinical phase II trial.
我们采用了人肿瘤克隆形成试验(HTCA),作为一种面向疾病的新型抗肿瘤药物筛选模型,来测试FR66973的抗肿瘤活性,并将其活性与其类似化合物丝裂霉素C进行比较。FR66973针对从非小细胞肺癌(NSCLC)患者获取的新鲜肿瘤细胞的总体体外反应率(定义为肿瘤集落形成单位存活率低于50%),在浓度为0.1、1和10微克/毫升时分别为32%、50%和89%,在相应浓度下优于丝裂霉素C。我们的数据表明,FR66973是一种有前景的抗NSCLC新药。如果I期毒性不是禁忌,FR66973在临床II期试验中可能对NSCLC也具有良好活性。