Booth Christopher M, Calvert A Hilary, Giaccone Giuseppe, Lobbezoo Marinus W, Eisenhauer Elizabeth A, Seymour Lesley K
National Cancer Institute of Canada Clinical Trials Group, Queen's University, Kingston, ON, Canada.
Eur J Cancer. 2008 Jan;44(1):25-9. doi: 10.1016/j.ejca.2007.07.031. Epub 2007 Sep 12.
The Methodology for the Development of Innovative Cancer Therapies (MDICT) task force considered aspects of the design and conduct of phase II studies for molecular targeted agents during their 2007 meeting. The task force recommended that multinomial endpoints and designs should be considered for phase II studies of targeted agents, that both single arm as well as randomised designs remain appropriate in certain settings, and that further assessment of novel endpoints (tumour growth kinetic assessment, biomarker or functional imaging) and designs (randomised discontinuation or Bayesian adaptive design) be encouraged. The MDICT cautioned on the use of small randomised trials which have a number of statistical pitfalls and dangers and strongly encouraged the complete reporting, including negative trials, in the scientific literature.
创新癌症治疗方法开发方法学(MDICT)特别工作组在其2007年会议期间审议了分子靶向药物II期研究的设计与实施方面的问题。特别工作组建议,对于靶向药物的II期研究应考虑多项终点和设计,在某些情况下单臂设计和随机设计仍然适用,并且鼓励进一步评估新的终点(肿瘤生长动力学评估、生物标志物或功能成像)和设计(随机停药或贝叶斯适应性设计)。MDICT对存在诸多统计缺陷和风险的小型随机试验的使用提出了警告,并强烈鼓励在科学文献中完整报告研究结果,包括阴性试验。