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CPT-11及其活性代谢产物SN-38的临床前评估。

Preclinical evaluation of CPT-11 and its active metabolite SN-38.

作者信息

Lavelle F, Bissery M C, André S, Roquet F, Riou J F

机构信息

Rhône-Poulenc Rorer R&D, Centre de Recherche de Vitry-Alfortville, Vitry-sur-Seine, France.

出版信息

Semin Oncol. 1996 Feb;23(1 Suppl 3):11-20.

PMID:8633248
Abstract

CPT-11 (irinotecan) is a water-soluble analogue of camptothecin (CPT), an antitumor drug extracted from the Chinese tree Camptotheca acuminata. SN-38 is an active metabolite of CPT-11 that contributes significantly to its activity. The antitumor effects of CPT-11 and SN-38 are exerted through a novel mechanism of action; inhibition of DNA topoisomerase I. CPT-11 and its metabolite have demonstrated potent inhibitory activity against a variety of cancer cell lines in vitro and against several murine and human tumors grafted in mice in vivo, including those that express multidrug resistance. CPT-11 has also shown synergistic activity in combination with 5-fluorouracil and cisplatin in vitro. No irreversible or unusual toxicities were observed with CPT-11 in animal toxicity studies. In summary, the preclinical profile of CPT-11 confirmed this drug to be an attractive candidate for clinical development.

摘要

CPT-11(伊立替康)是喜树碱(CPT)的水溶性类似物,喜树碱是一种从中国树木喜树中提取的抗肿瘤药物。SN-38是CPT-11的活性代谢产物,对其活性有显著贡献。CPT-11和SN-38的抗肿瘤作用是通过一种新的作用机制发挥的;抑制DNA拓扑异构酶I。CPT-11及其代谢产物在体外对多种癌细胞系以及在体内对移植到小鼠体内的几种小鼠和人类肿瘤均显示出强大的抑制活性,包括那些表达多药耐药性的肿瘤。CPT-11在体外与5-氟尿嘧啶和顺铂联合使用时也显示出协同活性。在动物毒性研究中,未观察到CPT-11有不可逆或异常毒性。总之,CPT-11的临床前研究资料证实该药物是临床开发中一个有吸引力的候选药物。

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