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首页> 外文期刊>Gastric cancer: official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association >Randomized phase II study of sequential docetaxel and irinotecan with 5-fluorouracil/folinic acid (leucovorin) in patients with advanced gastric cancer: the GATAC trial.
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Randomized phase II study of sequential docetaxel and irinotecan with 5-fluorouracil/folinic acid (leucovorin) in patients with advanced gastric cancer: the GATAC trial.

机译:序贯多西紫杉醇和伊立替康与5-氟尿嘧啶/亚叶酸(亚叶酸)在晚期胃癌患者中的随机II期研究:GATAC试验。

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BACKGROUND: The optimal chemotherapy in patients with advanced gastric carcinoma (GC) is yet to be determined. We compared sequential administration of docetaxel and irinotecan, both in combination with infused 5-fluorouracil/leucovorin (5-Fu/Lv), and randomly assigned patients to start with either of the two. METHODS: Patients with previously untreated locally advanced or metastatic GC and with measurable lesions (response evaluation criteria in solid tumors; RECIST) were randomly assigned to start with docetaxel 45 mg/m(2) (arm T) or irinotecan 180 mg/m(2) (arm C) with bolus/44-h infusion of 5-Fu/Lv (day 1 every 2 weeks). After four courses, there was a prescheduled crossover to the alternative regimen for four additional courses. RESULTS: Eighty-one patients were randomized and 78 started treatment. Complete and partial responses were seen in 31 (40%) patients after 8 weeks and in 32 (41%) after 16 weeks, with similar results in both study arms. The median overall survival (OS) was 11.5 and 10.6 months in arms T and C, respectively (P = 0.3). The two schedules were feasible and did not differ in the overall rate of severe adverse events (SAEs). CONCLUSION: This is the first randomized comparison of two of the newer cytostatic drugs in GC therapy. No differences favoring either arm T or arm C were found with respect to response rate, OS, or toxicity. The median OS of 11 months indicates that sequential administration of the two combinations is effective and is similar to triple combinations. Thus, comparable efficacy to platinum combinations appears to be obtained with newer, less toxic regimens when given sequentially.
机译:背景:晚期胃癌(GC)患者的最佳化疗方案尚待确定。我们比较了多西他赛和伊立替康的顺序给药方法,两者均与输注的5-氟尿嘧啶/亚叶酸钙(5-Fu / Lv)组合使用,并随机分配了患者以两者中的任一个开始。方法:随机分配先前未经治疗的局部晚期或转移性GC且可测量的病灶(实体瘤反应评估标准; RECIST)的患者,以多西他赛45 mg / m(2)(T型臂)或伊立替康180 mg / m( 2)(C组)推注/ 44小时内输注5-Fu / Lv(每2周第1天)。经过四门课程后,针对其他四门课程的替代方案进行了预先安排的转换。结果:81例患者被随机分配并开始治疗78例。 8周后在31例(40%)患者中观察到完全和部分反应,而16周后在32例(41%)中观察到,两个研究组的结果相似。 T组和C组的中位总生存期(OS)分别为11.5和10.6个月(P = 0.3)。这两个时间表是可行的,并且在严重不良事件(SAE)的总体发生率方面没有差异。结论:这是GC疗法中两种新的抑制细胞生长药物的首次随机比较。在应答率,OS或毒性方面,未发现有利于T臂或C臂的差异。中位OS为11个月,表明两种组合的顺序给药是有效的,并且类似于三联组合。因此,当相继给予时,似乎用较新的,毒性较小的方案可获得与铂组合物相当的功效。

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