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首页> 外文期刊>Contemporary Clinical Trials Communications >A statistical approach to identify optimal inclusion criteria: An application to acute stroke clinical trials
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A statistical approach to identify optimal inclusion criteria: An application to acute stroke clinical trials

机译:确定最佳纳入标准的统计方法:在急性中风临床试验中的应用

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PurposeTo develop a statistical approach that compares patient selection strategies across clinical trials and apply this approach to acute ischemic stroke clinical trials to identify the optimal inclusion criteria.MethodsWe developed a statistical approach that compares the number needed to treat to achieve one success (NNT) along with the number needed to screen to achieve one success (NNS) and assesses if there are significant differences in inclusion criteria, treatment course, and clinical outcome among patients that may have been included/excluded in the trials. We applied this approach to the study population from four recent positive acute stroke clinical trials: MR CLEAN, EXTEND-IA, ESCAPE, and SWIFT PRIME, applying published trial criteria to an independent registry of 612 acute stroke patients, since we did not have access to the complete trial data.ResultsAlthough reported NNT were similar for EXTEND-IA, SWIFT PRIME and ESCAPE, and somewhat higher for MR CLEAN, NNS varied across the trials from 21 for EXTEND-IA, 27 for MR CLEAN, to 46 for ESCAPE and 64 for SWIFT PRIME, reflecting less and more stringent inclusion criteria, respectively. Although there were significant differences in imaging biomarkers and other clinical characteristics among patients that may have been included/excluded in the trials, these differences did not translate to significant differences in treatment course or clinical outcomes.ConclusionsOur study proposes a robust statistical approach that can be applied to a larger pooled trial dataset, if made available, to objectively compare across clinical trials and inform inclusion criteria of future trials. Pooled analysis of the acute stroke trial data is needed to determine which imaging biomarker inclusion criteria are critical and which may be relaxed. If this procedure were applied across the pooled trial data, it could decrease costs and refine the design of future trials to be the most efficacious for the greatest number of patients.
机译:目的开发一种统计方法来比较整个临床试验中的患者选择策略,并将该方法应用于急性缺血性中风临床试验中,以确定最佳的纳入标准。方法我们开发了一种统计方法,该方法比较了获得成功(NNT)所需的治疗数量筛查以取得一项成功(NNS)所需的人数,并评估试验中可能包括/排除的患者的入选标准,治疗过程和临床结果是否存在显着差异。我们将这种方法应用于最近的四个阳性急性卒中临床试验的研究人群:MR CLEAN,EXTEND-IA,ESCAPE和SWIFT PRIME,并将已发布的试验标准应用于612例急性卒中患者的独立登记册,因为我们无法获得结果尽管EXTEND-IA,SWIFT PRIME和ESCAPE的报告NNT相似,而MR CLEAN更高,但NNS在整个试验中有所不同,从EXTEND-IA的21个,MR CLEAN的27个到ESCAPE和46个的NNT都不同。 SWIFT PRIME的64,分别反映了越来越少的严格纳入标准。尽管在试验中可能包括/排除的患者中成像生物标志物和其他临床特征存在显着差异,但这些差异并未转化为治疗过程或临床结果的显着差异。结论我们的研究提出了一种可靠的统计学方法,可以应用于更大的合并试验数据集(如果有的话),以客观地比较临床试验并告知未来试验的纳入标准。需要对急性中风试验数据进行汇总分析,以确定哪些成像生物标志物纳入标准至关重要,哪些可以放宽。如果将此程序应用于汇总的试验数据,则可以降低成本并完善未来试验的设计,使其对最多的患者最有效。

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