Novel chemotherapeutic agents in colorectal cancer

被引:6
|
作者
Napier, MP [1 ]
Ledermann, JA [1 ]
机构
[1] UCL Hosp, Myerstein Inst Oncol, Dept Oncol, London W1N 8AA, England
来源
EUROPEAN JOURNAL OF SURGICAL ONCOLOGY | 2000年 / 26卷 / 06期
基金
英国医学研究理事会;
关键词
colorectal cancer; chemotherapy; thymidylate synthase; oxaliplatin; irinotecan; capecitabine;
D O I
10.1053/ejso.2000.0955
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer remains the second most common cause of cancer death in Europe. A number of new agents, with varying mechanisms of action, have been developed and are being evaluated, both as single agents and in combination. Irinotecan, a topisomerase I inhibitor, and oxaliplatin, a new platinum compound, have proven efficacy in advanced colorectal cancer resistant to 5-fluorouracil, Capecitabine and other oral fluoro-pyrimidines are also emerging as potentially effective drugs. Raltitrexed and other inhibitors of thymidylate synthase (TS) are entering clinical practice although their role has yet to be determined. The new fluoro-pyrimidines and TS inhibitors are important classes of drug which have been designed to take advantage of the knowledge of folate metabolism gained from basic clinical research. Their design features could perhaps reduce the toxicity seen with the first generation cytotoxic agents. This review will focus on these new chemotherapeutic agents in colorectal cancer with respect to their mechanisms of action, current clinical activity and their potential use both in the adjuvant and palliative settings.
引用
收藏
页码:605 / 610
页数:6
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