Gerrits C J, de Jonge M J, Schellens J H, Stoter G, Verweij J
Department of Medical Oncology, Rotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital, The Netherlands.
Br J Cancer. 1997;76(7):952-62. doi: 10.1038/bjc.1997.491.
Topoisomerase I inhibitors constitute a new class of anti-cancer agents. Recently, topotecan and irinotecan were registered for clinical use in ovarian cancer and colorectal cancer respectively. Cytotoxicity of topoisomerase I inhibitors is S-phase specific, and in vitro and in vivo studies have suggested that, for efficacy, prolonged exposure might be more important than short-term exposure to high concentration. Clinical development of those topoisomerase I inhibitors that have reached this stage is also focused on schedules aiming to achieve prolonged exposure. In this review, we summarize all published preclinical studies on this topic for topoisomerase I inhibitors in clinical development, namely 20-S-camptothecin, 9-nitro-camptothecin, 9-amino-camptothecin, topotecan, irinotecan and GI147211. In addition, preliminary data on clinical studies concerning this topic are also reviewed. The data suggest that prolonged exposure may indeed be relevant for anti-tumour activity. However, the optimal schedule is yet to be determined. Finally, clinical data are yet too immature to draw definitive conclusions.
拓扑异构酶I抑制剂构成了一类新型抗癌药物。最近,拓扑替康和伊立替康分别被批准用于卵巢癌和结直肠癌的临床治疗。拓扑异构酶I抑制剂的细胞毒性具有S期特异性,体外和体内研究表明,为了达到疗效,长时间暴露可能比短期高浓度暴露更为重要。已进入该阶段的那些拓扑异构酶I抑制剂的临床开发也集中在旨在实现长时间暴露的给药方案上。在本综述中,我们总结了所有已发表的关于处于临床开发阶段的拓扑异构酶I抑制剂(即20-S-喜树碱、9-硝基喜树碱、9-氨基喜树碱、拓扑替康、伊立替康和GI147211)这一主题的临床前研究。此外,还综述了有关该主题的临床研究的初步数据。数据表明,长时间暴露可能确实与抗肿瘤活性相关。然而,最佳给药方案尚未确定。最后,临床数据还不够成熟,无法得出明确结论。