Novel anti-cancer agents in development: exciting prospects and new challenges

被引:52
作者
Seymour, L [1 ]
机构
[1] Queens Univ, Natl Canc Inst Canada, Clin Trials Grp, Kingston, ON K7L 3N6, Canada
关键词
phase I; phase II; novel; matrix metalloproteinase inhibitors; nucleoside analogues; signal transduction inhibition; epidermal growth factor receptor;
D O I
10.1053/ctrv.1999.0134
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A large number of cancer chemotherapeutic agents, are in development, many already undergoing clinical testing. A number of these compounds were designed either to modulate or inhibit molecular targets which have been identified as being critical to the development or control of cancer. Targets for inhibition include matrix metalloproteinases, mediators of signal transduction (tyrosine kinases, cyclin dependent kinases and other kinases such as protein kinase C and A) as well as ros expression and prenylation. Classes of potential inhibitory compounds include small molecules. humanized monoclonal antibodies or antisense oligonucleotides. Many of these compounds are relatively well advanced in development. Proof of principle has already been demonstrated in some instances and at least one such compound has been approved for use. Although these new compounds offer exciting opportunities, many bring with them real challenges in terms of the selection of appropriate trial design and surrogate end-points. (C) 1999 Harcourt Publishers Ltd.
引用
收藏
页码:301 / 312
页数:12
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