Napier M P, Ledermann J A
Department of Oncology, Myerstein Institute of Oncology, University College London Hospitals, Mortimer Street, London, W1N 8AA, UK.
Eur J Surg Oncol. 2000 Sep;26(6):605-10. doi: 10.1053/ejso.2000.0955.
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.
在欧洲,结直肠癌仍是癌症死亡的第二大常见原因。已研发出多种作用机制各异的新型药物,这些药物正作为单一药物或联合用药进行评估。伊立替康(一种拓扑异构酶I抑制剂)和奥沙利铂(一种新型铂类化合物)已证实对耐5-氟尿嘧啶的晚期结直肠癌有效。卡培他滨和其他口服氟嘧啶类药物也逐渐成为潜在的有效药物。雷替曲塞和其他胸苷酸合成酶(TS)抑制剂正在进入临床实践,尽管它们的作用尚未确定。新型氟嘧啶类药物和TS抑制剂是重要的药物类别,它们是利用基础临床研究中获得的叶酸代谢知识设计而成的。其设计特点或许能降低第一代细胞毒性药物所出现的毒性。本综述将聚焦于这些用于结直肠癌的新型化疗药物,涉及其作用机制、当前临床活性以及它们在辅助治疗和姑息治疗中的潜在用途。