首页> 外文期刊>BMC Medicine >A randomized phase III trial of adjuvant chemotherapy with irinotecan, leucovorin and fluorouracil versus leucovorin and fluorouracil for stage II and III colon cancer: A Hellenic Cooperative Oncology Group study
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A randomized phase III trial of adjuvant chemotherapy with irinotecan, leucovorin and fluorouracil versus leucovorin and fluorouracil for stage II and III colon cancer: A Hellenic Cooperative Oncology Group study

机译:伊立替康,亚叶酸和氟尿嘧啶与亚叶酸和氟尿嘧啶辅助化疗的II期和III期结肠癌的随机III期临床试验:希腊合作肿瘤小组研究

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Background Colon cancer is a public health problem worldwide. Adjuvant chemotherapy after surgical resection for stage III colon cancer has been shown to improve both progression-free and overall survival, and is currently recommended as standard therapy. However, its value for patients with stage II disease remains controversial. When this study was designed 5-fluorouracil (5FU) plus leucovorin (LV) was standard adjuvant treatment for colon cancer. Irinotecan ( CPT-11 ) is a topoisomerase I inhibitor with activity in metastatic disease. In this multicenter adjuvant phase III trial, we evaluated the addition of irinotecan to weekly 5FU plus LV in patients with stage II or III colon cancer. Methods The study included 873 eligible patients. The treatment consisted of weekly administration of irinotecan 80 mg/m2 intravenously (IV), LV 200 mg/m2 and 5FU 450 mg/m2 bolus (Arm A) versus LV 200 mg/m2 and 5FU 500 mg/m2 IV bolus (Arm B). In Arm A, treatments were administered weekly for four consecutive weeks, followed by a two-week rest, for a total of six cycles, while in Arm B treatments were administered weekly for six consecutive weeks, followed by a two-week rest, for a total of four cycles. The primary end-point was disease-free survival (DFS) at three years. Results The probability of overall survival (OS) at three years was 0.88 for patients in Arm A and 0.86 for those in Arm B, while the five-year OS probability was 0.78 and 0.76 for patients in Arm A and Arm B, respectively (P = 0.436). Furthermore, the probability of DFS at three years was 0.78 and 0.76 for patients in Arm A and Arm B, respectively ( P = 0.334). With the exception of leucopenia and neutropenia, which were higher in patients in Arm A, there were no significant differences in Grades 3 and 4 toxicities between the two regimens. The most frequently recorded Grade 3/4 toxicity was diarrhea in both treatment arms. Conclusions Irinotecan added to weekly bolus 5FU plus LV did not result in improvement in disease-free or overall survival in stage II or III colon cancer, but did increase toxicity. Trial registration Australian New Zealand Clinical Trials Registry: ACTRN12610000148077
机译:背景技术结肠癌是全世界的公共卫生问题。业已证明,III期结肠癌手术切除后的辅助化疗可改善无进展生存期和总体生存期,目前建议作为标准疗法。但是,其对II期疾病患者的价值仍存在争议。设计该研究时,5-氟尿嘧啶(5FU)加亚叶酸(LV)是结肠癌的标准辅助治疗方法。伊立替康(CPT-11)是一种拓扑异构酶I抑制剂,在转移性疾病中具有活性。在这项多中心辅助III期试验中,我们评估了II期或III期结肠癌患者每周5FU加LV加伊立替康的可能性。方法该研究纳入了873名符合条件的患者。该治疗包括每周静脉注射伊立替康80 mg / m 2 ,LV 200 mg / m 2 和5FU 450 mg / m 2 推注(Arm A)与LV 200 mg / m 2 和5FU 500 mg / m 2 IV推注(手臂B)。在A组,每周连续四周进行治疗,然后休息两周,共六个周期,而在B组中,每周连续六周进行治疗,然后连续两周休息。总共四个周期。主要终点是三年的无病生存期(DFS)。结果A组患者三年总生存率(OS)为0.88,B组患者为0.86,而A组和B组患者五年生存率分别为0.78和0.76(P = 0.436)。此外,A组和B组患者三年DFS的概率分别为0.78和0.76(P = 0.334)。除了白血球减少症和中性粒细胞减少症(A组患者较高)外,两种治疗方案的3级和4级毒性没有显着差异。记录最频繁的3/4级毒性是两个治疗组的腹泻。结论伊立替康每周推注5FU加LV并不能改善II期或III期结肠癌的无病生存期或总生存期,但确实会增加毒性。试验注册澳大利亚新西兰临床试验注册:ACTRN12610000148077

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