With the rapid development of new anti-cancer agents which are cytostatic, new endpoints are needed to better measure treatment efficacy in phase II trials. For this purpose, Von Hoff (1998) proposed the growth modulation index (GMI), i.e. the ratio between times to progression or progression-free survival times in two successive treatment lines. An essential task in studies using GMI as an endpoint is to estimate the distribution of GMI. Traditional methods for survival data have been used for estimating the GMI distribution because censoring is common for GMI data. However, we point out that the independent censoring assumption required by traditional survival methods is always violated for GMI, which may lead to severely biased results. In this paper, we construct nonparametric estimators for the distribution of GMI, accounting for the dependent censoring of GMI. We prove that the proposed estimators are consistent and converge weakly to zero-mean Gaussian processes upon proper normalization. Extensive simulation studies show that our estimators perform well in practical situations and outperform traditional methods. A phase II clinical trial using GMI as the primary endpoint is provided for illustration.
翻译:随着新抗癌剂的迅速发展,需要新的终点来更好地衡量第二阶段试验的治疗效果。为此目的,Von Hoff(1998年)提议了增长调控指数(GMI),即连续两条治疗线中增长调控指数(GMI)与进步或无进步生存时间的比率。将GMI作为终点的研究的一项基本任务是估计GMI的分布情况。由于对GMI数据进行检查是常见的,所以使用传统的生存数据方法来估计GMI的分布情况。然而,我们指出,传统生存方法所要求的独立审查假设总是被违反,这可能导致严重偏差的结果。在本文件中,我们为GMI的分布建立了非参数性估算器,以核算对GMI进行依赖性审查的情况。我们证明,拟议的估算器在适当正常化之后,与零度高斯进程相容弱。广泛的模拟研究表明,我们的估量器在实际情况下表现良好,超越了传统方法。我们用GMI作为主要终点的第二阶段临床试验是用来说明的。