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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >A randomized phase III study comparing adjuvant 5-fluorouracil/folinic acid with FOLFIRI in patients following complete resection of liver metastases from colorectal cancer.
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A randomized phase III study comparing adjuvant 5-fluorouracil/folinic acid with FOLFIRI in patients following complete resection of liver metastases from colorectal cancer.

机译:一项III期随机研究,在完全切除结直肠癌肝转移患者后,将5-氟尿嘧啶/亚叶酸佐剂与FOLFIRI进行了比较。

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BACKGROUND: Studies indicate that adjuvant 5-fluorouracil (5-FU) with folinic acid (FA) in colorectal cancer patients with completely resectable liver-limited metastases (LMCRC) offers clinical benefit over surgery alone. This phase III trial compared FOLFIRI with simplified 5-FU/FA in this setting. PATIENTS AND METHODS: LMCRC patients were randomized to receive every 14 days, FA, 400 mg/m2 infused over 2 h, followed by 5-FU as a 400 mg/m2 i.v. bolus, followed by continuous 5-FU infusion, 2400 mg/m2 over 46 h (LV5FUs) with or without irinotecan: 180 mg/m2 infusion (FOLFIRI). The primary end point was disease-free survival (DFS); secondary end points included overall survival (OS) and safety. RESULTS: Treated patients (n = 306) were balanced for critical prognostic factors in each arm. Median DFS in patients receiving LV5FUs was 21.6 versus 24.7 months for FOLFIRI [hazard ratio (HR) 0.89, log-rank P = 0.44]. No significant differences were found in OS. A trend was observed for improved DFS in patients receiving FOLFIRI within 42 days of surgery (HR 0.75, P = 0.17). Grade 3/4 toxic effects were more common in patients treated with FOLFIRI versus LV5FUs (47% versus 30%) with neutropenia being most common (23% versus 7%). CONCLUSION: FOLFIRI in the adjuvant treatment of LMCRC showed no significant improvement in DFS compared with LV5FUs.
机译:背景:研究表明,对于具有完全可切除的肝脏有限转移灶(LMCRC)的结直肠癌患者,佐剂5-氟尿嘧啶(5-FU)与亚叶酸(FA)相比单纯手术可提供临床益处。这项III期试验将FOLFIRI与简化的5-FU / FA在这种情况下进行了比较。患者与方法:LMCRC患者随机分组,每14天接受FA,每2小时输注400 mg / m2,然后静脉输注400 mg / m2的5-FU。推注,然后连续5-FU输注,在46小时内连续2400 mg / m2(LV5FUs),有或没有伊立替康:180 mg / m2输注(FOLFIRI)。主要终点是无病生存期(DFS)。次要终点包括总体生存期(OS)和安全性。结果:治疗的患者(n = 306)在各组的关键预后因素方面保持平衡。接受LV5FU的患者的DFS中位数为21.6个月,而FOLFIRI为24.7个月[危险比(HR)0.89,对数秩P = 0.44]。在操作系统中没有发现显着差异。观察到在手术后42天内接受FOLFIRI的患者DFS改善的趋势(HR 0.75,P = 0.17)。 FOLFIRI治疗组与LV5FU治疗组相比,3/4级毒性作用更为常见(47%对30%),中性粒细胞减少症最为常见(23%对7%)。结论:与LV5FU相比,FOLFIRI在LMCRC的辅助治疗中未显示DFS的显着改善。

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