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拓扑异构酶I抑制剂。喜树碱类似物概述。

Topoisomerase I inhibitors. An overview of the camptothecin analogs.

作者信息

Burris H A, Fields S M

机构信息

Institute for Drug Development, Cancer Therapy and Research Center, San Antonio, Texas.

出版信息

Hematol Oncol Clin North Am. 1994 Apr;8(2):333-55.

PMID:8040144
Abstract

The topoisomerase I inhibitors are an exciting new class of antineoplastic agents currently under clinical development. Analogues of camptothecin with improved toxicity profiles and antitumor activity included CPT-11 and topotecan. CPT-11 has demonstrated activity against a variety of tumor types, particularly colon and lung cancer. Early results with topotecan against ovarian and lung cancer are also encouraging. Combination trials with other antineoplastic agents including cisplatin and etoposide, and early clinical trials with new topoisomerase I inhibitors, such as 9-aminocamptothecin, are underway.

摘要

拓扑异构酶I抑制剂是目前正在临床开发中的一类令人兴奋的新型抗肿瘤药物。具有改善的毒性特征和抗肿瘤活性的喜树碱类似物包括CPT-11和拓扑替康。CPT-11已显示出对多种肿瘤类型有效,尤其是结肠癌和肺癌。拓扑替康治疗卵巢癌和肺癌的早期结果也令人鼓舞。与包括顺铂和依托泊苷在内的其他抗肿瘤药物的联合试验,以及与新型拓扑异构酶I抑制剂如9-氨基喜树碱的早期临床试验正在进行中。

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