首页> 美国卫生研究院文献>Annals of Surgery >A prospective randomized trial of regional versus systemic continuous 5-fluorodeoxyuridine chemotherapy in the treatment of colorectal liver metastases.
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A prospective randomized trial of regional versus systemic continuous 5-fluorodeoxyuridine chemotherapy in the treatment of colorectal liver metastases.

机译:区域性与全身性连续5-氟脱氧尿苷化疗治疗结直肠肝转移的前瞻性随机试验。

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摘要

Sixty-four patients were entered into a randomized trial that evaluated intra-arterial (I.A.) versus intravenous (I.V.) 5-fluorodeoxyuridine (FUDR) for colorectal liver metastases. There was a significant improved response rate for I.A. (62%) compared with I.V. (17%) treatment (p less than 0.003). However, the improved response rate for patients in whom I.A. therapy was used did not translate to a significantly improved survival rate. The 2-year actuarial survival rates for the groups for which I.A. and I.V. therapy was used were 22% and 15% respectively, with the survival curves not differing significantly (p = 0.27). These results may have been due to the inclusion of patients with tumor in draining hepatic lymph nodes. The presence of tumor in hepatic lymph nodes was associated with a poorer prognosis. Analysis of a subgroup of patients with negative hepatic lymph nodes suggested an improved actuarial survival rate in patients for whom I.A. versus I.V. therapy was used (p less than 0.03). The toxicity of I.A. FUDR was considerable, and side effects included chemical hepatitis (79%), biliary sclerosis (21%), peptic ulcers (17%), and gastritis/duodenitis (21%). The only major effect of toxicity of I.V. FUDR was severe diarrhea (59%). Regional I.A. FUDR allowed more drug delivery to liver tumors, which resulted in increased tumor responses when compared with use of systemic therapy. However, the small gain in survival seen in a select subgroup of patients with negative hepatic nodes appeared to be offset by the toxicity of I.A. FUDR.
机译:六十四名患者进入一项随机试验,评估了动脉内(I.A.)与静脉内(I.V.)5-氟脱氧尿苷(FUDR)的结直肠肝转移。 I.A.的回应率有了明显提高。 (62%)与I.V. (17%)治疗(p小于0.003)。但是,对I.A.患者的缓解率有所提高使用该疗法并未转化为明显提高的生存率。 I.A.组的2年精算生存率和IV两种疗法的使用率分别为22%和15%,生存曲线无显着差异(p = 0.27)。这些结果可能是由于引流性肝淋巴结肿大的肿瘤患者所致。肝淋巴结中存在肿瘤与预后较差有关。对肝淋巴结阴性患者亚组的分析表明,接受I.A.治疗的患者精算存活率提高了。与I.V.使用了疗法(p小于0.03)。 I.A.的毒性FUDR相当大,其副作用包括化学性肝炎(79%),胆汁性硬化症(21%),消化性溃疡(17%)和胃炎/十二指肠炎(21%)。静脉曲张毒性的唯一主要作用FUDR为严重腹泻(59%)。区域I.A.与全身疗法相比,FUDR可以将更多的药物递送至肝肿瘤,从而导致肿瘤反应增加。但是,在肝结节阴性的特定患者亚组中看到的小幅生存增加似乎被I.A.的毒性所抵消。 FUDR。

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