Randall-Whitis Leslie M, Monk Bradley J
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, University of California, Irvine, 101 The City Dr South, Bldg 56, Suite 210, Orange, CA 92868, USA.
Expert Opin Pharmacother. 2007 Feb;8(2):227-36. doi: 10.1517/14656566.8.2.227.
Topotecan, a semisynthetic camptothecin, exerts its cytotoxic effect through inhibition of DNA topoisomerase I. Single-agent topotecan has demonstrated activity against persistent, metastatic and recurrent cancer of the uterine cervix. When combined with cisplatin in Phase II trials, further improved response rates have been reported. The cisplatin/topotecan doublet subsequently proved to be the first regimen in a series of multiple Phase III studies to demonstrate improved disease-free and overall survival in this setting compared with cisplatin alone, thus leading to its third indication by both the US FDA and the European Medicines Agency in 2006. This survival advantage was achieved at the expense of an increase in grade 3-4 hematologic toxicity; however, there was no difference in patient-reported quality of life between the cisplatin/topotecan doublet and single-agent cisplatin. This article reviews the pharmacology of topotecan and its evolution as an active agent in advanced and metastatic cervical cancer that is not amenable to cure with surgery or radiotherapy.
拓扑替康是一种半合成喜树碱,通过抑制DNA拓扑异构酶I发挥其细胞毒性作用。单药拓扑替康已显示出对持续性、转移性和复发性宫颈癌的活性。在II期试验中与顺铂联合使用时,据报道缓解率进一步提高。顺铂/拓扑替康双联疗法随后在一系列多项III期研究中被证明是首个与单独使用顺铂相比能在此情况下改善无病生存期和总生存期的方案,因此在2006年被美国食品药品监督管理局和欧洲药品管理局批准为其第三个适应症。这种生存优势是以3-4级血液学毒性增加为代价实现的;然而,顺铂/拓扑替康双联疗法与单药顺铂之间患者报告的生活质量并无差异。本文综述了拓扑替康的药理学及其作为晚期和转移性宫颈癌活性药物的演变,这类癌症无法通过手术或放疗治愈。