Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109-2029, USA.
Biostatistics. 2011 Apr;12(2):258-69. doi: 10.1093/biostatistics/kxq054. Epub 2010 Aug 25.
The Superior Yield of the New Strategy of Enoxaparin, Revascularization, and GlYcoprotein IIb/IIIa inhibitors (SYNERGY) was a randomized, open-label, multicenter clinical trial comparing 2 anticoagulant drugs on the basis of time-to-event endpoints. In contrast to other studies of these agents, the primary, intent-to-treat analysis did not find evidence of a difference, leading to speculation that premature discontinuation of the study agents by some subjects may have attenuated the apparent treatment effect and thus to interest in inference on the difference in survival distributions were all subjects in the population to follow the assigned regimens, with no discontinuation. Such inference is often attempted via ad hoc analyses that are not based on a formal definition of this treatment effect. We use SYNERGY as a context in which to describe how this effect may be conceptualized and to present a statistical framework in which it may be precisely identified, which leads naturally to inferential methods based on inverse probability weighting.
新策略依诺肝素、血运重建和糖蛋白 IIb/IIIa 抑制剂(SYNERGY)的卓越产量是一项随机、开放标签、多中心临床试验,比较了基于时间事件终点的两种抗凝药物。与这些药物的其他研究不同,主要的、意向治疗分析并未发现差异的证据,这导致了一些猜测,即一些受试者过早停止使用研究药物可能削弱了明显的治疗效果,因此人们对在没有停药的情况下,所有受试者均遵循分配方案的情况下,对生存分布差异的推断感兴趣。这种推断通常通过非特殊分析来尝试,这些分析不是基于这种治疗效果的正式定义。我们使用 SYNERGY 作为一个背景,在这个背景下描述这种效果是如何被概念化的,并提出一个统计框架,在这个框架中可以精确地识别这种效果,这自然导致了基于逆概率加权的推断方法。