首页> 美国卫生研究院文献>Springer Open Choice >The IDEA (International Duration Evaluation of Adjuvant Chemotherapy) Collaboration: Prospective Combined Analysis of Phase III Trials Investigating Duration of Adjuvant Therapy with the FOLFOX (FOLFOX4 or Modified FOLFOX6) or XELOX (3 versus 6 months) Regimen for Patients with Stage III Colon Cancer: Trial Design and Current Status
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The IDEA (International Duration Evaluation of Adjuvant Chemotherapy) Collaboration: Prospective Combined Analysis of Phase III Trials Investigating Duration of Adjuvant Therapy with the FOLFOX (FOLFOX4 or Modified FOLFOX6) or XELOX (3 versus 6 months) Regimen for Patients with Stage III Colon Cancer: Trial Design and Current Status

机译:IDEA(国际辅助化疗持续时间评估)合作:III期试验的前瞻性联合分析研究针对III期结肠癌患者的FOLFOX(FOLFOX4或改良的FOLFOX6)或XELOX(3个月至6个月)方案的辅助治疗的持续时间的III期试验:试验设计与现状

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摘要

The International Duration Evaluation of Adjuvant Chemotherapy (IDEA) collaboration was established to prospectively combine and analyze data from several randomized trials conducted around the world to answer whether a three-month course of oxaliplatin-based adjuvant therapy (FOLFOX4/modified FOLFOX6 or XELOX) is non-inferior to the current standard six-month treatment for patients with stage III colon cancer, with a primary endpoint of three years disease-free survival. The IDEA steering committee comprises two members from each group coordinating an individual trial and two members from a secretariat who coordinate combining of the data and management of the joint analysis. Members of the IDEA agreed to combine the data from their individual trials to enable definitive analysis consisting of at least 10,500 patients. With accrual of 8,797 patients at the end of February 2013, the IDEA is on track to achieve its accrual objective of at least 10,500 patients by the end of 2013.
机译:建立了国际辅助化疗持续时间评估(IDEA)合作,以前瞻性地合并和分析来自世界各地进行的几项随机试验的数据,以回答是否以奥沙利铂为基础的辅助治疗(FOLFOX4 /改良的FOLFOX6或XELOX)三个月疗程对于III期结肠癌患者,治疗效果不逊于当前标准的六个月治疗,其主要终点是三年无病生存期。 IDEA指导委员会由每个小组的两名成员协调一个独立的试验,并由秘书处的两名成员协调数据的合并和联合分析的管理。 IDEA的成员同意将他们各自试验的数据进行合并,以进行至少10,500名患者的明确分析。截止到2013年2月,IDEA的累计应征人数为8797名患者,IDEA有望在2013年底之前实现其至少10500名病人的应聘目标。

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