Suppr超能文献

临床等效性试验中的当前问题。

Current issues in clinical equivalence trials.

作者信息

Blackwelder W C

出版信息

J Dent Res. 2004;83 Spec No C:C113-5. doi: 10.1177/154405910408301s23.

Abstract

A clinical trial designed to show that an experimental treatment E is similar to a control treatment S in a specified direction is a one-sided equivalence or similarity trial--in the terminology of the International Conference on Harmonisation, a non-inferiority trial (ICH, 1998). We design such a study to show that E is not worse than S (often an accepted or standard treatment) by as much as a pre-specified margin theta0. The quantity theta0 can be either a difference or ratio of an appropriate outcome in individuals treated with E and S. A critical issue is whether one can conclude from a non-inferiority trial that E is effective. Closely related is an appropriate choice of theta0, which should be substantially less than the estimated effect of S if available from previous studies; theta0 should also be acceptable to clinicians, either because of advantages of E or because a difference or ratio less than theta0 is considered unimportant clinically. Another possible approach for showing that E is effective is to estimate its effect compared with placebo from historical data. If previous studies that consistently show an effect of S are not available, alternative study designs should be considered. Findings of superiority or non-inferiority of E, when the study was planned to show the other, are possible and may be supportable. A finding that E is at the same time statistically significantly worse than S and "non-inferior" to S should not be a problem, if the criterion theta0 is appropriate and this possibility was considered in the protocol. Various sorts of non-adherence may make treatments appear similar, even if they are not. In particular, random non-adherence of study participants to the assigned treatment regimen may cause an intention-to-treat analysis to give a misleading result of similarity. Thus, maintaining a high degree of adherence to protocol is especially important in an equivalence or non-inferiority trial. Interim analysis does not present statistical problems in these trials; early stopping may not be wise in many cases, however, because strong interim evidence for non-inferiority may actually be an indicator that E is superior to S.

摘要

一项旨在表明实验性治疗E在特定方向上与对照治疗S相似的临床试验是单侧等效性或相似性试验——按照国际协调会议的术语,即非劣效性试验(ICH,1998)。我们设计这样一项研究,以表明E不比S(通常是已被接受的或标准的治疗方法)差超过预先指定的界限θ0。量θ0可以是接受E和S治疗的个体中适当结局的差值或比值。一个关键问题是,能否从非劣效性试验得出E是有效的结论。与之密切相关的是θ0的适当选择,如果能从先前的研究中获得S的估计效应,那么θ0应远小于该估计效应;θ0也应能被临床医生接受,这要么是因为E的优势,要么是因为小于θ0的差值或比值在临床上被认为不重要。另一种表明E有效的可能方法是根据历史数据估计其与安慰剂相比的效应。如果没有始终显示S有疗效的先前研究,就应考虑其他研究设计。当研究计划显示E的优越性时,却发现E具有非劣效性,或者当研究计划显示E的非劣效性时,却发现E具有优越性,这些情况都是有可能的,而且可能是有依据的。如果标准θ0合适且方案中考虑了这种可能性,那么发现E在统计学上显著比S差同时又“非劣效于”S不应成为问题。各种不依从情况可能会使治疗看起来相似,即使它们实际上并非如此。特别是,研究参与者对分配的治疗方案的随机不依从可能会导致意向性分析给出相似性的误导性结果。因此,在等效性或非劣效性试验中,保持对方案的高度依从尤为重要。中期分析在这些试验中不存在统计学问题;然而,在许多情况下提前终止试验可能并不明智,因为非劣效性的有力中期证据实际上可能表明E优于S。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验