医学
限制
拓扑异构酶
最大耐受剂量
心脏毒性
毒性
中性粒细胞减少症
药理学
药品
内科学
胃肠病学
肿瘤科
DNA
机械工程
遗传学
工程类
生物
作者
Carola A.S. Arndt,Mark Krailo,Wen Liu‐Mares,Peter M. Anderson,Gregory H. Reaman
出处
期刊:Cancer
[Wiley]
日期:2001-01-01
卷期号:91 (6): 1166-1169
被引量:3
标识
DOI:10.1002/1097-0142(20010315)91:6<1166::aid-cncr1113>3.0.co;2-y
摘要
BACKGROUND CI-958 is a synthetic intercalating agent of a new chemical class, the benzopyranoindazoles, with promising preclinical activity. Its mechanism of action is thought to be stabilization of the cleavable complex of DNA with topoisomerase II, as well as DNA helicase blockade. It is thought to have less cardiotoxicity than the anthracyclines. Early Phase I studies in adults showed the drug to be well tolerated, making it an attractive agent to pursue in Phase I clinical trials in children. METHODS Children and adolescents with recurrent solid tumors received CI-958 at an initial dose of 450 mg/m2 over 2 hours. Dose escalation was performed in a standard fashion in cohorts of three patients until dose limiting toxicity and the maximum tolerated dose were determined. RESULTS Twenty-one patients were entered on the study. The maximum tolerated dose was found to be 650 mg/m2. Dose limiting toxicities were Grade 4 neutropenia and Grade 4 hypotension at the dose level of 700 mg/m2. CONCLUSIONS The maximum tolerated dose of CI-958 in children and adolescents is 650 mg/m2. No antitumor activity has been observed. Cancer 2001;91:1166–9. © 2001 American Cancer Society.
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