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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。

Irinotecan plus oxaliplatin: a promising combination for advanced colorectal cancer.

作者信息

Wasserman E, Sutherland W, Cvitkovic E

机构信息

Cvitkovic & Associés Consultants, Argentina, Echeverria 1442, E.P. of 49 (1428), Buenos Aires, Argentina.

出版信息

Clin Colorectal Cancer. 2001 Nov;1(3):149-53. doi: 10.3816/CCC.2001.n.015.

DOI:10.3816/CCC.2001.n.015
PMID:12450427
Abstract

The standard treatment for advanced colorectal cancer (CRC) has been 5-fluorouracil (5-FU)-based chemotherapy. However, addition of irinotecan, a topoisomerase I inhibitor, to the combination of 5-FU and leucovorin (LV) has proven to be superior to treatment with 5-FU/LV alone in both chemonaive as well as previously treated patients. Oxaliplatin, a 1,2 diaminocyclohexane platinum compound, in combination with 5-FU and LV, has demonstrated superiority as first-line therapy over 5-FU and LV in terms of response rate and time to progression. The irinotecan/oxaliplatin combination showed synergistic activity in vitro, and the optimal dose safety profile has been explored in several phase I studies. Neutropenia and diarrhea were the dose-limiting toxicities. The recommended dose of irinotecan/oxaliplatin in every-2-week and every-3-week schedules ranged from 150-200 mg/m2 and 85 mg/m2, respectively. In the weekly schedule, the recommended doses of irinotecan/oxaliplatin were 65 mg/m2 and 60 mg/m2. Promising clinical efficacy in CRC was observed in all studies. A recent randomized phase II study revealed that the irinotecan/oxaliplatin combination has equivalent clinical activity to other 5-FU-based combinations and a manageable toxicity profile. The evaluation of irinotecan/oxaliplatin in phase III trials as well as in combination with 5-FU is ongoing.

摘要

晚期结直肠癌(CRC)的标准治疗方法一直是以5-氟尿嘧啶(5-FU)为基础的化疗。然而,在5-FU和亚叶酸钙(LV)联合方案中加入拓扑异构酶I抑制剂伊立替康,已被证明在初治患者以及既往接受过治疗的患者中均优于单纯5-FU/LV治疗。奥沙利铂,一种1,2-二氨基环己烷铂化合物,与5-FU和LV联合使用,在缓解率和疾病进展时间方面作为一线治疗已显示出优于5-FU和LV。伊立替康/奥沙利铂联合方案在体外显示出协同活性,并且在几项I期研究中探索了最佳剂量安全性。中性粒细胞减少和腹泻是剂量限制性毒性。伊立替康/奥沙利铂在每2周和每3周给药方案中的推荐剂量分别为150-200mg/m²和85mg/m²。在每周给药方案中,伊立替康/奥沙利铂的推荐剂量分别为65mg/m²和60mg/m²。在所有研究中均观察到结直肠癌有良好的临床疗效。最近一项随机II期研究表明,伊立替康/奥沙利铂联合方案具有与其他基于5-FU的联合方案相当的临床活性以及可控的毒性特征。伊立替康/奥沙利铂在III期试验以及与5-FU联合使用的评估正在进行中。

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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.
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Irinotecan, oxaliplatin plus bolus 5-fluorouracil and low dose folinic acid every 2 weeks: a feasibility study in metastatic colorectal cancer patients.伊立替康、奥沙利铂联合推注5-氟尿嘧啶及小剂量亚叶酸钙,每2周一次:转移性结直肠癌患者的一项可行性研究。
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Efficacy of treatment with irinotecan and oxaliplatin combination in FU-resistant metastatic colorectal cancer patients.伊立替康与奥沙利铂联合治疗对氟尿嘧啶耐药的转移性结直肠癌患者的疗效
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A phase II study of irinotecan alternated with a weekly schedule of oxaliplatin, high-dose leucovorin and 48-hour infusion 5-fluorouracil in patients with advanced colorectal cancer.伊立替康与奥沙利铂每周方案、高剂量亚叶酸钙及48小时持续输注5-氟尿嘧啶交替使用治疗晚期结直肠癌的II期研究。
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Phase I and pharmacokinetic study of two different schedules of oxaliplatin, irinotecan, Fluorouracil, and leucovorin in patients with solid tumors.奥沙利铂、伊立替康、氟尿嘧啶和亚叶酸钙两种不同给药方案用于实体瘤患者的I期及药代动力学研究
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Irinotecan, oxaliplatin, and 5-fluorouracil/leucovorin combination chemotherapy in advanced colorectal carcinoma: a phase II study.伊立替康、奥沙利铂和5-氟尿嘧啶/亚叶酸联合化疗用于晚期结直肠癌:一项II期研究。
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Mortality associated with daily bolus 5-fluorouracil/leucovorin administered in combination with either irinotecan or oxaliplatin: results from Intergroup Trial N9741.与每日推注5-氟尿嘧啶/亚叶酸联合伊立替康或奥沙利铂给药相关的死亡率:来自组间试验N9741的结果
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Current status of capecitabine in the treatment of colorectal cancer.卡培他滨在结直肠癌治疗中的现状
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Irinotecan or oxaliplatin combined with leucovorin and 5-fluorouracil as first-line treatment in advanced colorectal cancer: a multicenter, randomized, phase II study.伊立替康或奥沙利铂联合亚叶酸钙和5-氟尿嘧啶作为晚期结直肠癌一线治疗的多中心、随机、II期研究。
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The use of irinotecan, oxaliplatin and raltitrexed for the treatment of advanced colorectal cancer: systematic review and economic evaluation.伊立替康、奥沙利铂和雷替曲塞用于治疗晚期结直肠癌:系统评价与经济学评估
Health Technol Assess. 2008 May;12(15):iii-ix, xi-162. doi: 10.3310/hta12150.

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