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喜树碱类的临床应用。

Clinical applications of the camptothecins.

作者信息

Takimoto C H, Wright J, Arbuck S G

机构信息

Developmental Therapeutics Department, Medicine Branch, Division of Clinical Sciences, National Cancer Institute, Building 8, Room 5101, Bethesda Naval Hospital, Bethesda, MD 20892, USA.

出版信息

Biochim Biophys Acta. 1998 Oct 1;1400(1-3):107-19. doi: 10.1016/s0167-4781(98)00130-4.

Abstract

The camptothecin topoisomerase I-targeting agents are new class of antitumor drugs with demonstrated clinical activity in human malignancies, such as colorectal cancer and ovarian cancer. Currently, irinotecan and topotecan are the most widely used camptothecin analogs in clinical use and clinical trials are ongoing to better characterize their spectra of clinical activity, to determine their optimal schedules of administration and to define their use in combination with other chemotherapeutic agents. Newer camptothecin analogs in clinical development, such as 9-aminocamptothecin, 9-nitrocamptothecin, GI147211 and DX-8951f, are also being studied to determine if they have improved toxicity and efficacy profiles compared with existing analogs. Other potential clinical applications include the use of camptothecin derivatives as radiation sensitizers or as antiviral agents. The successful development of the camptothecins as antitumor agents highlights the importance of topoisomerase I as a target for cancer chemotherapy.

摘要

喜树碱类拓扑异构酶I靶向药物是一类新型抗肿瘤药物,已在人类恶性肿瘤(如结直肠癌和卵巢癌)中显示出临床活性。目前,伊立替康和拓扑替康是临床应用中使用最广泛的喜树碱类似物,正在进行临床试验,以更好地描述其临床活性谱,确定其最佳给药方案,并确定它们与其他化疗药物联合使用的情况。正在临床开发中的新型喜树碱类似物,如9-氨基喜树碱、9-硝基喜树碱、GI147211和DX-8951f,也在进行研究,以确定它们与现有类似物相比是否具有改善的毒性和疗效特征。其他潜在的临床应用包括将喜树碱衍生物用作放射增敏剂或抗病毒剂。喜树碱作为抗肿瘤药物的成功开发突出了拓扑异构酶I作为癌症化疗靶点的重要性。

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