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伊立替康(CPT-11)对恶性神经外胚层肿瘤实验模型的抗肿瘤作用。

Antitumoral effect of irinotecan (CPT-11) on an experimental model of malignant neuroectodermal tumor.

作者信息

Morales C, Zurita M, Vaquero J

机构信息

Laboratory of Experimental Neuro-Oncology, Neuroscience Research Unit of the Mapfre-Medicine Foundation, Puerta de Hierro Clinic, Autonomous University, Madrid, Spain.

出版信息

J Neurooncol. 2002 Feb;56(3):219-26. doi: 10.1023/a:1015014623569.

Abstract

Irinotecan (CPT-11) is a topoisomerase I inhibitor with antitumor activity on a wide variety of neoplasms in several preclinical studies, but it showed poor efficacy in patients with nervous system tumors. We have carried out an experimental study in order to evaluate the effect of CPT-11 on the growth of a subcutaneously implanted malignant neuroectodermal tumor, after administration by different routes. The results showed that CPT-11 administration by intraperitoneal injections (at dose 10 mg/kg, 5 days per week, for 2 weeks, followed by 7-days rest period--one course--to a total of two courses) had no significant antitumor effect. Nevertheless, continuous infusion by intraperitoneal osmotic minipump over 28 days (at an infusion rate of 4.4 microg/h) showed a significant delay in tumor growth in 4 weeks of the implantation. The best antitumor effects were observed after CPT-11 intratumoral administration (at dose of 5 mg/kg, 5 days per week, for 2 weeks, followed by 7-days rest period, to a total of three courses) reaching tumor regression in the treated animals. These results suggest the utility of CPT-11, by means of intralesional administration, on malignant tumors of the nervous system.

摘要

伊立替康(CPT - 11)是一种拓扑异构酶I抑制剂,在多项临床前研究中对多种肿瘤具有抗肿瘤活性,但在神经系统肿瘤患者中疗效不佳。我们进行了一项实验研究,以评估不同给药途径后CPT - 11对皮下植入的恶性神经外胚层肿瘤生长的影响。结果表明,腹腔注射CPT - 11(剂量为10 mg/kg,每周5天,共2周,随后休息7天——一个疗程——共两个疗程)没有显著的抗肿瘤作用。然而,通过腹腔渗透微型泵持续输注28天(输注速率为4.4微克/小时)显示,在植入后的4周内肿瘤生长明显延迟。CPT - 11瘤内给药(剂量为5 mg/kg,每周5天,共2周,随后休息7天,共三个疗程)后观察到最佳抗肿瘤效果,治疗的动物出现肿瘤消退。这些结果表明,通过瘤内给药方式,CPT - 11对神经系统恶性肿瘤具有应用价值。

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