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首页> 外文期刊>Journal of neuro-oncology. >Use of different outcome measures in randomised studies of malignant glioma can significantly alter the interpretation of time to progression: reanalysis of the MRC BR2 study.
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Use of different outcome measures in randomised studies of malignant glioma can significantly alter the interpretation of time to progression: reanalysis of the MRC BR2 study.

机译:在恶性神经胶质瘤的随机研究中使用不同的结局指标可显着改变进展时间的解释:MRC BR2研究的重新分析。

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摘要

The Medical Research Council (MRC) BR2 study [1] is a randomised trial of two doses of cranial radiation for patients with malignant glioma. We reanalysed data to examine the effect of using change in ranked scales of neurological status (MRC Neurological Status Scale) and performance (World Health Organisation Scale: WHO) to determine progression rather than clinician's impression. Four hundred and seventy four patients were studied. Where clinicians recorded no progression, ranked scales frequently documented progression (MRC 13%; WHO 13%). Where clinicians recorded progression, ranked scales frequently did not alter (MRC 33%; WHO 30%) or occasionally improved (MRC 5%; WHO 3%). When analysing time to progression based on a variety of measures, the estimated difference between treatments was most extreme (hazard ratio 0.81, logrank p = 0.04) when change in WHO status was used, and least extreme when change in MRC neurological status was used (hazard ratio 0.99, p = 0.94). This study highlights how different outcome measures can significantly alter the interpretation of randomised studies.
机译:医学研究理事会(MRC)的BR2研究[1]是针对恶性神经胶质瘤患者进行两次颅脑辐射剂量的随机试验。我们重新分析了数据,以检验使用神经状态排名量表(MRC神经状态量表)和表现(世界卫生组织量表:WHO)的变化来确定进展而非临床医生的印象所产生的影响。研究了474例患者。在临床医生没有进展的地方,排名量表经常记录进展(MRC 13%; WHO 13%)。在临床医生记录病情进展的地方,分级量表通常不会改变(MRC 33%; WHO 30%)或偶尔有所改善(MRC 5%; WHO 3%)。当基于多种方法分析进展时间时,使用WHO状况变化时,治疗之间的估计差异最大(风险比0.81,对数秩p = 0.04),而使用MRC神经系统状况变化时,估计之间的差别最小((危险比0.99,p = 0.94)。这项研究强调了不同的结局指标如何显着改变随机研究的解释。

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