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首页> 外文期刊>Cancer chemotherapy and pharmacology. >Combination chemotherapy of biweekly irinotecan (CPT-11) plus tegafur/uracil (UFT) and leucovorin (LV) for patients with metastatic colorectal cancer: phase I/II study in Japanese patients.
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Combination chemotherapy of biweekly irinotecan (CPT-11) plus tegafur/uracil (UFT) and leucovorin (LV) for patients with metastatic colorectal cancer: phase I/II study in Japanese patients.

机译:转移性结直肠癌患者每两周一次依立替康(CPT-11)联合替加氟/尿嘧啶(UFT)和亚叶酸(LV)联合化疗:日本患者的I / II期研究。

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摘要

PURPOSE: We aimed to evaluate the safety and efficacy of combination chemotherapy with biweekly irinotecan (CPT-11) plus oral tegafur/uracil (UFT) and leucovorin (LV) in patients with previously untreated metastatic colorectal adenocarcinoma in phase I/II setting. PATIENTS AND METHODS: We recruited 37 patients with histologically proven metastatic colorectal adenocarcinoma. UFT (300 mg/m(2) per day) and LV (75 mg/day) were administered orally on days 1-21. CPT-11 was administered intravenously on day 1 and 15, at an initial dose of 60 mg/m(2), stepping up to 150 mg/m(2) in a traditional phase I fashion. The treatment was repeated every 4 weeks. After patients enrolled into a phase II portion, the efficacy and toxicity of this regimen were also assessed. RESULTS: The recommended dose of CPT-11 was determined to be 150 mg/m(2). Although one patient had a pulmonary embolism after 60 mg/m(2) of CPT-11, the treatment was well tolerated in general. The overall objective response rate was 37.8% (14/37; 95% CI, 22.5-55.2) in all patients. Median progression-free survival was 226 days (95% CI, 133-276). CONCLUSIONS: Biweekly CPT-11 plus UFT and LV had a reasonable safety profile with manageable toxicity, and had a promising activity in patients with metastatic colorectal cancer. Further trials are indicated based on the promising results observed in this study.
机译:目的:我们的目的是评估I / II期转移性结直肠腺癌未经治疗的患者,每两周一次伊立替康(CPT-11)联合口服替加氟/尿嘧啶(UFT)和亚叶酸(LV)联合化疗的安全性和有效性。患者与方法:我们招募了37例经组织学证实为转移性结直肠腺癌的患者。在第1至21天口服UFT(每天300 mg / m(2))和LV(每天75 mg)。 CPT-11在第1天和第15天静脉注射,初始剂量为60 mg / m(2),以传统的I期方式逐步增加至150 mg / m(2)。每4周重复一次治疗。患者进入II期部分后,还评估了该方案的疗效和毒性。结果:确定的CPT-11推荐剂量为150 mg / m(2)。尽管一名患者在60 mg / m(2)的CPT-11后出现肺栓塞,但总体上该治疗耐受良好。所有患者的总客观缓解率为37.8%(14/37; 95%CI,22.5-55.2)。中位无进展生存期为226天(95%CI,133-276)。结论:每两周一次的CPT-11联合UFT和LV具有安全性合理,毒性可控的特点,对转移性结直肠癌患者具有良好的活性。根据这项研究中观察到的有希望的结果,表明了进一步的试验。

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