Future directions for clinical research with CPT-11 (irinotecan)

被引:9
|
作者
VonHoff, D
机构
[1] Institute for Drug Development, Texas Research Park, 14960 Omicron Park, San Antonio
关键词
CPT-11; topoisomerase I; clinical trials; phase I; phase II; human tumour cloning assay; preclinical;
D O I
10.1016/0959-8049(96)00291-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CPT-11 is a new agent with a unique mechanism of action, namely the inhibition of topoisomerase I. An examination of data from the laboratory reveals several leads which should be pursued in the clinic. A dose-response effect for CPT-11 activity has been noted in the human tumour cloning assay. CPT-11 has activity against breast and mesothelioma colony-forming units in a human tumour cloning assay, and has in vivo activity against a number of paediatric malignancies. Promising combinations in preclinical in vivo models include CPT-11/mitomycin C and CPT-11/cytosine arabinoside. There is incomplete cross-resistance among topoisomerase I inhibitors, suggesting that combinations of topoisomerase I inhibitors should be investigated. Several natural products have been identified which have potential to decrease CPT-ll-induced diarrhoea. The level of carboxylesterase in a patient's tumour appears to be related to the in vitro activity of CPT-11, suggesting that measurement of carboxylesterase in a patient's tumour could be used to identify patients who are most likely to respond to treatment with CPT-11. These preclinical findings suggest substantial further clinical potential for CPT-11 in terms of decreased CPT-ll-induced diarrhoea as well as increased antitumour activity, which should be explored in phase I and II studies. Copyright (C) 1996 Published by Elsevier Science Ltd
引用
收藏
页码:S9 / S12
页数:4
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