A Threshold Regression Mixture Model for Assessing Treatment Efficacy in a Multiple Myeloma Clinical Trial

被引:14
作者
Lee, Mei-Ling Ting [1 ]
Chang, Mark [2 ]
Whitmore, G. A. [3 ]
机构
[1] Univ Maryland, Sch Publ Hlth, Dept Epidemiol & Biostat, College Pk, MD 20742 USA
[2] Millennium Pharmaceut Inc, Cambridge, MA USA
[3] McGill Univ, Montreal, PQ, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Analysis time; Composite time; Cox regression; Data analysis; Disease progression; Duration; First hitting time; Lifetime; Maximum likelihood; Mixture model; Multiple myeloma; Proportional hazards; Randomized clinical trial; Stochastic process; Stopping time; Survival; Threshold regression; Time-to-event; Treatment switching; Wiener diffusion process;
D O I
10.1080/10543400802398524
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A first-hitting-time (FHT) survival model postulates a health status process for a patient that gradually declines until the patient dies when the level first reaches a critical threshold. Threshold regression (TR) is a new regression methodology that incorporates the effects of covariates on the threshold and process parameters of this FHT model. In this study, we use TR to analyze data from a randomized clinical trial of treatment for multiple myeloma. The trial compares VELCADE and high-dose Dexamethasone, the former a new therapy and the latter an established therapy for this disease. Patients are switched between the two drugs based on patient response. The novel contribution of this work is the modeling of this clinical trial design using a mixture of TR models. Specifically, we propose a mixture FHT model to fit the survival distribution. The model includes a composite time scale that differentiates the rate of disease progression before and after switching. The analysis shows significant benefit from initial treatment by VELCADE. A comparison is made with a Cox proportional hazards regression analysis of the same data.
引用
收藏
页码:1136 / 1149
页数:14
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