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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.

DOI:10.1016/0959-8049(96)00294-8
PMID:8943662
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。

相似文献

1
CPT-11 (irinotecan) and 5-fluorouracil: a promising combination for therapy of colorectal cancer.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。
Eur J Cancer. 1996;32A Suppl 3:S24-31. doi: 10.1016/0959-8049(96)00294-8.
2
[Standard therapy of CPT-11 for colorectal cancer].[伊立替康治疗结直肠癌的标准疗法]
Gan To Kagaku Ryoho. 2001 Oct;28(10):1345-51.
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Efficacy of CPT-11 (irinotecan) as a single agent in metastatic colorectal cancer.
Eur J Cancer. 1996;32A Suppl 3:S13-7. doi: 10.1016/0959-8049(96)00292-4.
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Current status of colorectal cancer: CPT-11 (irinotecan), a therapeutic innovation.
Eur J Cancer. 1996;32A Suppl 3:S1-8. doi: 10.1016/0959-8049(96)00290-0.
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Irinotecan plus fluorouracil/leucovorin for metastatic colorectal cancer: a new survival standard.伊立替康联合氟尿嘧啶/亚叶酸钙治疗转移性结直肠癌:一种新的生存标准。
Oncologist. 2001;6(1):81-91. doi: 10.1634/theoncologist.6-1-81.
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[Combination of 5-Fluorouracil and folinic acid--is it still the standard therapy for advanced colorectal carcinoma?].[5-氟尿嘧啶与亚叶酸联合应用——它仍是晚期结直肠癌的标准治疗方法吗?]
Tumori. 2000 Sep-Oct;86(5 Suppl 2):S19-25.
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Bimonthly chemotherapy with oxaliplatin, irinotecan, infusional 5-fluorouracil/folinic acid in patients with metastatic colorectal cancer pretreated with irinotecan- or oxaliplatin-based chemotherapy.对接受过基于伊立替康或奥沙利铂化疗的转移性结直肠癌患者,每两个月使用奥沙利铂、伊立替康、持续输注5-氟尿嘧啶/亚叶酸进行化疗。
J Chemother. 2008 Oct;20(5):622-31. doi: 10.1179/joc.2008.20.5.622.
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Irinotecan plus oxaliplatin: a promising combination for advanced colorectal cancer.伊立替康联合奥沙利铂:晚期结直肠癌的一种有前景的联合方案。
Clin Colorectal Cancer. 2001 Nov;1(3):149-53. doi: 10.3816/CCC.2001.n.015.
9
Role of chemotherapy for advanced colorectal cancer: new opportunities.
Semin Oncol. 1996 Feb;23(1 Suppl 3):42-50.
10
[Current evidence of irinotecan combination chemotherapy with TS-1 in patients with advanced colorectal cancer].
Gan To Kagaku Ryoho. 2006 Jul;33(7):896-900.

引用本文的文献

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Overcoming Therapy Resistance in Colorectal Cancer: Targeting the Rac1 Signaling Pathway as a Potential Therapeutic Approach.克服结直肠癌的治疗抵抗:以 Rac1 信号通路为靶点的潜在治疗方法。
Cells. 2024 Oct 26;13(21):1776. doi: 10.3390/cells13211776.
2
The effective combination therapies with irinotecan for colorectal cancer.伊立替康用于结直肠癌的有效联合疗法。
Front Pharmacol. 2024 Feb 5;15:1356708. doi: 10.3389/fphar.2024.1356708. eCollection 2024.
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Individualization of Irinotecan Treatment: A Review of Pharmacokinetics, Pharmacodynamics, and Pharmacogenetics.
个体化伊立替康治疗:药代动力学、药效学和药物遗传学综述。
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Systemic treatment-induced gastrointestinal toxicity: incidence, clinical presentation and management.全身治疗引起的胃肠道毒性:发生率、临床表现及管理
Ann Gastroenterol. 2012;25(2):106-118.
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Clin Colon Rectal Surg. 2005 Aug;18(3):215-23. doi: 10.1055/s-2005-916282.
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Cancer chemotherapy-induced diarrhoea and constipation: mechanisms of damage and prevention strategies.癌症化疗引起的腹泻和便秘:损伤机制及预防策略。
Support Care Cancer. 2006 Sep;14(9):890-900. doi: 10.1007/s00520-006-0040-y. Epub 2006 Apr 8.