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首页> 外文期刊>BMC Cancer >Study protocol of the SACURA trial: a randomized phase III trial of efficacy and safety of UFT as adjuvant chemotherapy for stage II colon cancer
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Study protocol of the SACURA trial: a randomized phase III trial of efficacy and safety of UFT as adjuvant chemotherapy for stage II colon cancer

机译:SACURA试验的研究方案:UFT作为II期结肠癌辅助化疗的有效性和安全性的随机III期试验

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Background Adjuvant chemotherapy for stage III colon cancer is internationally accepted as standard treatment with established efficacy, but the usefulness of adjuvant chemotherapy for stage II colon cancer remains controversial. The major Western guidelines recommend adjuvant chemotherapy for “high-risk stage II” cancer, but this is not clearly defined and the efficacy has not been confirmed. Methods/design SACURA trial is a multicenter randomized phase III study which aims to evaluate the superiority of 1-year adjuvant treatment with UFT to observation without any adjuvant treatment after surgery for stage II colon cancer in a large population, and to identify “high-risk factors of recurrence/death” in stage II colon cancer and predictors of efficacy and adverse events of the chemotherapy. Patients aged between 20 and 80?years with curatively resected stage II colon cancer are randomly assigned to a observation group or UFT adjuvant therapy group (UFT at 500–600?mg/day as tegafur in 2 divided doses after meals for 5?days, followed by 2-day rest. This 1-week treatment cycle is repeated for 1?year). The patients are followed up for 5?years until recurrence or death. Treatment delivery and adverse events are entered into a web-based case report form system every 3?months. The target sample size is 2,000 patients. The primary endpoint is disease-free survival, and the secondary endpoints are overall survival, recurrence-free survival, and incidence and severity of adverse events. In an additional translational study, the mRNA expression of 5-FU-related enzymes, microsatellite instability and chromosomal instability, and histopathological factors including tumor budding are assessed to evaluate correlation with recurrences, survivals and adverse events. Discussion A total of 2,024 patients were enrolled from October 2006 to July 2010. The results of this study will provide important information that help to improve the therapeutic strategy for stage II colon cancer. Trial registration ClinicalTrials.gov NCT00392899.
机译:背景技术III期结肠癌的辅助化疗已被国际公认是具有确定疗效的标准治疗方法,但II期结肠癌的辅助化疗的有效性仍存在争议。西方主要指南建议对“高危II期”癌症进行辅助化疗,但这尚无明确定义,疗效尚未得到证实。方法/设计SACURA试验是一项多中心随机III期研究,旨在评估使用UFT进行1年辅助治疗对大量人群II期结肠癌术后无辅助治疗观察的优越性,并确定“高II期结肠癌复发/死亡的危险因素”和化疗疗效和不良事件的预测指标。年龄在20至80岁之间且已根治性切除的II期结肠癌的患者被随机分配到观察组或UFT辅助治疗组(UFT剂量为500–600?mg /天的替加福,分2餐后分5天服用,然后休息2天,这个1周的治疗周期重复1年。对患者进行5年随访,直至复发或死亡。每3个月将治疗提供和不良事件输入基于Web的病例报告表格系统。目标样本量为2,000名患者。主要终点是无病生存期,次要终点是总体生存期,无复发生存期以及不良事件的发生率和严重性。在另一项翻译研究中,评估了5-FU相关酶的mRNA表达,微卫星不稳定性和染色体不稳定性以及包括肿瘤萌芽在内的组织病理学因素,以评估其与复发,存活和不良事件的相关性。讨论从2006年10月到2010年7月,总共招募了2,024名患者。这项研究的结果将提供有助于改善II期结肠癌治疗策略的重要信息。试用注册ClinicalTrials.gov NCT00392899。

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