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伊立替康(CPT-11)与5-氟尿嘧啶:一种有前景的结直肠癌治疗联合方案。

CPT-11 (irinotecan) and 5-fluorouracil: a promising combination for therapy of colorectal cancer.

作者信息

Saltz L, Shimada Y, Khayat D

机构信息

Memorial Sloan-Kettering Cancer Center, New York, New York, USA.

出版信息

Eur J Cancer. 1996;32A Suppl 3:S24-31. doi: 10.1016/0959-8049(96)00294-8.

Abstract

CPT-11 (Campto, irinotecan) is a new topoisomerase I inhibitor and one of very few new cytotoxic agents to demonstrate clinical activity in colorectal cancer since the introduction of 5-fluorouracil (5-FU) into clinical practice almost 40 years ago. Because of the unique mechanism of action of CPT-11, its proven activity in colorectal cancer, and its lack of cross-resistance with 5-FU, the combination of CPT-11 with 5-FU is a logical approach to attempt to improve on the results obtained with CPT-11 or 5-FU-based treatments alone. Various administration schedules of CPT-11/5-FU combinations have been investigated in phase I studies in Japan, the U.S. and Europe. Preliminary results indicate that concurrent administration of substantial doses of CPT-11, 5-FU and folinic acid is feasible in terms of safety. Preliminary analysis of controlled pharmacokinetic data suggests that 5-FU has no substantial effect on the metabolism of CPT-11 to its active metabolite SN-38. Major objective responses and other indicators of clinical activity have been observed with the combination in both chemotherapy-naive and pretreated patients with colorectal cancer. Studies are ongoing to define fully optimum dosage schedules of CPT-11/5-FU combinations, and some of these schedules will soon enter phase II and III clinical trials. It is hoped that such a combination will prove to be an important advance in the treatment of colorectal cancer.

摘要

CPT-11(开普拓,伊立替康)是一种新型拓扑异构酶I抑制剂,自近40年前5-氟尿嘧啶(5-FU)应用于临床以来,它是为数不多的在结直肠癌中显示出临床活性的新型细胞毒性药物之一。由于CPT-11独特的作用机制、在结直肠癌中已证实的活性以及与5-FU不存在交叉耐药性,CPT-11与5-FU联合使用是一种合理的方法,有望改善单独使用CPT-11或基于5-FU的治疗所取得的疗效。在日本、美国和欧洲进行的I期研究中,对CPT-11/5-FU联合用药的各种给药方案进行了研究。初步结果表明,同时给予大剂量的CPT-11、5-FU和亚叶酸在安全性方面是可行的。对对照药代动力学数据的初步分析表明,5-FU对CPT-11代谢为其活性代谢产物SN-38没有实质性影响。在未经化疗和经预处理的结直肠癌患者中,联合用药均观察到了主要客观反应和其他临床活性指标。目前正在进行研究以全面确定CPT-11/5-FU联合用药的最佳剂量方案,其中一些方案将很快进入II期和III期临床试验。希望这种联合用药将被证明是结直肠癌治疗的一项重要进展。

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