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首页> 外文期刊>International journal of colorectal disease. >Adjuvant perioperative portal vein or peripheral intravenous chemotherapy for potentially curative colorectal cancer: long-term results of a randomized controlled trial.
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Adjuvant perioperative portal vein or peripheral intravenous chemotherapy for potentially curative colorectal cancer: long-term results of a randomized controlled trial.

机译:围手术期门静脉辅助化疗或外周静脉化疗可治疗潜在的结直肠癌:一项随机对照试验的长期结果。

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摘要

BACKGROUND AND AIMS: The perioperative use of a single course adjuvant portal vein infusion chemotherapy in patients with potentially curable colorectal cancer has been shown to significantly improve overall survival but did not reduce the occurrence of liver metastases (SAKK 40/81) [Swiss Group for Clinical Cancer Research (SAKK) Lancet 345(8946):349-353, 1995]. The objective of the present prospective, three-arm randomized multicenter trial was to assess whether peripheral venous administration of adjuvant chemotherapy regimen based on 5-fluorouracil (5-FU) and mitomycin C decreases the occurrence of liver metastases as well as prolongs disease-free and overall survival. MATERIALS AND METHODS: Stages I-III colorectal cancer patients (n = 753) were randomized to receive either surgery alone (control arm), surgery plus postoperative portal venous infusion of 5-FU 500 mg/m(2) plus heparin given for 24 hours for seven consecutive days plus mitomycin C 10 mg/m(2) given on the first day (arm 2), or surgeryand the same chemotherapy regimen administered by peripheral venous route (arm 3). RESULTS: The 5-year disease-free survival for the three treatment groups were 65% (control group), 60% (portal vein infusion, hazard ratio 1.18, p = 0.23), and 64% (intravenous infusion, hazard ratio 1.04, p = 0.76); the 5-year overall survival was 72% (control group), 69% (portal vein infusion, hazard ratio 1.21, p = 0.2), and 74% (intravenous infusion, hazard ratio 1.03, p = 0.86), respectively. A significant accumulation of early deaths were observed in the portal vein infusion group (p = 0.015). CONCLUSIONS: The present prospective randomized multicenter trial provides compelling evidence that short-term perioperative chemotherapy does not improve disease-free and overall survival in patients with potentially curative colorectal cancer. In contrary, the chemotherapy regimen administered in the present investigation seems to have potentially harmful effects, a finding which should be carefully considered in the planning of future trials. Postoperative short-term administration of 5-FU plus mitomycin C either through portal infusion or a central venous catheter is not recommended for routine use in patients with potentially curable colorectal cancer.
机译:背景与目的:已证明在可能治愈的结直肠癌患者中围手术期使用单疗程辅助门静脉输液化疗可显着提高总体生存率,但不会减少肝转移的发生率(SAKK 40/81)[瑞士研究小组临床癌症研究(SAKK)柳叶刀345(8946):349-353,1995]。本项前瞻性三臂随机多中心试验的目的是评估外周静脉给予基于5-氟尿嘧啶(5-FU)和丝裂霉素C的辅助化疗方案是否可以减少肝转移的发生并延长无病期和整体生存。材料与方法:I-III期大肠癌患者(n = 753)被随机分配接受单独手术(对照组),手术加术后5-FU 500 mg / m(2)的门静脉输注以及肝素治疗(24次)连续7天小时,并在第一天(第2组)给予丝裂霉素C 10 mg / m(2),或通过外周静脉途径进行手术和相同的化疗方案(第3组)。结果:三个治疗组的5年无病生存率分别为65%(对照组),60%(门静脉输液,危险比1.18,p = 0.23)和64%(静脉输液,危险比1.04, p = 0.76); 5年总生存率(对照组)为69%(门静脉输注,危险比1.21,p = 0.2)和74%(静脉输注,危险比1.03,p = 0.86)。在门静脉输注组中观察到大量早期死亡的累积(p = 0.015)。结论:本项前瞻性随机多中心试验提供了令人信服的证据,表明短期围手术期化疗不能改善潜在治愈性结直肠癌患者的无病生存期和总生存期。相反,在本研究中使用的化疗方案似乎具有潜在的有害作用,这一发现应在以后的试验计划中予以认真考虑。不建议在可能治愈的结直肠癌患者中常规使用门静脉输注或中心静脉导管对5-FU和丝裂霉素C进行术后短期给药。

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