首页> 美国卫生研究院文献>Orphanet Journal of Rare Diseases >A plea to provide best evidence in trials under sample-size restrictions: the example of pioglitazone to resolve leukoplakia and erythroplakia in Fanconi anemia patients
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A plea to provide best evidence in trials under sample-size restrictions: the example of pioglitazone to resolve leukoplakia and erythroplakia in Fanconi anemia patients

机译:恳求在样本量受限的试验中提供最佳证据:吡格列酮解决范可尼贫血患者白斑和红斑的例子

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摘要

In planning a clinical trial for demonstrating the efficacy of pioglitazone to resolve leukoplakia and erythroplakia in Fanconi anemia patients we had to discuss the need for a randomized controlled trial particularly under sample-size restrictions as very promising results were available from a single-arm clinical trial. Unfortunately, at a later stage, we had to suffer from the fact that single-arm clinical trials may sometimes mislead. When revisiting our planning at a later stage of a grant application, results of a randomized controlled trial had become available which were less impressive, but may still be of clinical interest. However, these results were perceived as disappointing in the light of previously raised hopes based on the results of the single-arm trial. We highlight some major problems when research is based on single-arm trials compared to randomized controlled trials. After debunking common arguments for the conduct of single-arm trials in rare disease we conclude that particularly in rare disease research should be based on randomized building blocks simply because more robust evidence is generated. The plea for single-arm trials should be substituted by a plea for cooperation of all stakeholders to provide best evidence for decision making under sample-size restrictions.
机译:在规划临床试验以证明吡格列酮解决范科尼贫血患者的白斑和红斑狼疮的功效时,我们必须讨论是否需要一项随机对照试验,尤其是在样本量有限的情况下,因为单臂临床试验可获得非常可喜的结果。不幸的是,在稍后的阶段,我们不得不忍受单臂临床试验有时会误导的事实。在拨款申请的后期阶段重新审查我们的计划时,已经获得了一项随机对照试验的结果,虽然效果不佳,但可能仍具有临床意义。但是,鉴于先前基于单臂试验结果提出的希望,这些结果被认为令人失望。当研究是基于单臂试验而不是随机对照试验时,我们强调了一些主要问题。在揭露了罕见疾病单臂试验进行的普遍论点之后,我们得出结论,特别是在罕见疾病研究中,仅应基于随机基础,因为会产生更可靠的证据。单臂试验的诉求应被所有利益相关者合作的诉求所代替,以为在样本量限制下的决策提供最佳证据。

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