Arkenau H T, Rettig K, Porschen R
Clinic of Internal Medicine, Hospital Bremen East, Züricher Strasse 40, 28325 Bremen, Germany.
Int J Colorectal Dis. 2005 May;20(3):258-61. doi: 10.1007/s00384-004-0657-6. Epub 2004 Nov 11.
Adjuvant postoperative treatment with 5-fluorouracil (5-FU) and leucovorin in curatively resected stage III colon cancer significantly reduces the risk of cancer recurrence and improves survival. The impact of continuous 5-FU with and without leucovorin on survival and tumor recurrence was analyzed in this study compared with the effects of bolus 5-FU/leucovorin.
Patients with a curatively resected UICC stage III colon cancer were stratified according to T, N and G category and randomly assigned to receive one of the three adjuvant treatment schemes: 5-FU 450 mg/m2 and leucovorin 100 mg/m2 x 5 days every 4 weeks; six cycles, arm A; 24-h infusion of high-dose 5-FU/leucovorin 2,600 mg/m2 and 500 mg/m2, two cycles of six applications, arm B; 24-h infusion of high-dose 5-FU 2,600 mg/m2, two cycles of six applications, arm C.
One hundred and forty-five patients enrolled into this study were eligible. To date, 28 patients have died; 9 on arm A, 11 on arm B, and 8 on arm C (P was nonsignificant). After a median follow-up time of 45 months, there was no statistical difference in survival and tumor recurrence between the three treatment arms. Adjuvant treatment in all arms was generally well tolerated; only a minority of patients experienced grade 3 and 4 toxicities.
There is no statistical difference in efficacy and toxicity in patients receiving either high-dose 5-FU with or without leucovorin or the standard 5-FU bolus regime after a curative resection of a stage III colon cancer.
在根治性切除的III期结肠癌患者中,术后使用5-氟尿嘧啶(5-FU)和亚叶酸进行辅助治疗可显著降低癌症复发风险并提高生存率。本研究分析了持续使用5-FU联合或不联合亚叶酸对生存和肿瘤复发的影响,并与推注5-FU/亚叶酸的效果进行比较。
将根治性切除的国际抗癌联盟(UICC)III期结肠癌患者根据T、N和G分类进行分层,并随机分配接受三种辅助治疗方案之一:5-FU 450 mg/m²和亚叶酸100 mg/m²,每4周5天;六个周期,A组;24小时输注高剂量5-FU/亚叶酸2600 mg/m²和500 mg/m²,两个周期,每个周期六次应用,B组;24小时输注高剂量5-FU 2600 mg/m²,两个周期,每个周期六次应用,C组。
145例患者纳入本研究,均符合条件。迄今为止,28例患者死亡;A组9例,B组11例,C组8例(P无统计学意义)。中位随访时间45个月后,三个治疗组在生存和肿瘤复发方面无统计学差异。所有组的辅助治疗耐受性一般良好;只有少数患者出现3级和4级毒性。
在III期结肠癌根治性切除术后,接受高剂量5-FU联合或不联合亚叶酸治疗或标准5-FU推注方案的患者在疗效和毒性方面无统计学差异。