Koblenz University of Applied Science, RheinAhrCampus Remagen, Joseph-Rovan-Allee 2, 53424, Remagen, Germany.
Institute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.
BMC Med Res Methodol. 2023 Apr 10;23(1):86. doi: 10.1186/s12874-023-01908-6.
In many clinical trials the study interest lies in the comparison of a treatment to a control group regarding a time to event endpoint like time to myocardial infarction, time to relapse, or time to a specific cause of death. Thereby, an event can occur before the primary event of interest that alters the risk for or prohibits observing the latter, i.e. a competing event. Furthermore, multi-center studies are often conducted. Hence, a cluster structure might be observed. However, commonly only the aspect of competing events or the aspect of the cluster structure is modelled within primary analysis, although both are given within the study design. Methods to adequately analyze data in such a design were recently described but were not systematically compared yet.
Within this work we provide a systematic comparison of four approaches for the analysis of competing events where a cluster structure is present based on a real life data set and a simulation study. The considered methods are the commonly applied cause-specific Cox proportional hazards model with a frailty, the Fine and Gray model for considering competing risks, and extensions of the latter model by Katsahian et al. and Zhou et al. RESULTS: Based on our simulation results, the model by Katsahian et al. showed the best performance in bias, square root of mean squared error, and power in nearly all scenarios. In contrast to the other three models this approach allows both unbiased effect estimation and prognosis.
The provided comparison and simulations help to guide applied researchers to choose an adequate method for the analysis of competing events where a cluster structure is present. Based on our simulation results the approach by Katsahian et al. can be recommended.
在许多临床试验中,研究兴趣在于比较治疗组与对照组的时间事件终点,如心肌梗死时间、复发时间或特定死亡原因时间。因此,事件可能在主要感兴趣事件之前发生,从而改变或阻止观察后者的风险,即竞争事件。此外,通常进行多中心研究。因此,可能会观察到聚类结构。然而,通常仅在主要分析中对竞争事件或聚类结构的方面进行建模,尽管在研究设计中都给出了这两个方面。最近描述了适当分析此类设计中数据的方法,但尚未对其进行系统比较。
在这项工作中,我们基于真实数据集和模拟研究,对存在聚类结构的竞争事件的四种分析方法进行了系统比较。所考虑的方法是常用的带有脆弱性的基于因果的 Cox 比例风险模型、用于考虑竞争风险的 Fine 和 Gray 模型,以及 Katsahian 等人和 Zhou 等人对后者模型的扩展。
基于我们的模拟结果,Katsahian 等人的模型在几乎所有情况下的偏差、均方根误差平方根和功效方面表现出最佳性能。与其他三个模型相比,该方法允许进行无偏的效果估计和预后。
提供的比较和模拟有助于指导应用研究人员选择适当的方法来分析存在聚类结构的竞争事件。基于我们的模拟结果,可以推荐 Katsahian 等人的方法。