Multilevel mixed effects parametric survival models using adaptive Gauss-Hermite quadrature with application to recurrent events and individual participant data meta-analysis

被引:62
作者
Crowther, Michael J. [1 ]
Look, Maxime P. [2 ]
Riley, Richard D. [3 ]
机构
[1] Univ Leicester, Dept Hlth Sci, Leicester LE1 7RH, Leics, England
[2] Erasmus Univ, Med Ctr, Erasmus MC Canc Inst, Dept Med Oncol, Rotterdam, Netherlands
[3] Univ Birmingham, Sch Hlth & Populat Sci, Birmingham B15 2TT, W Midlands, England
基金
英国医学研究理事会;
关键词
survival analysis; mixed effects; flexible parametric models; adaptive Gauss-Hermite quadrature; PATIENT DATA METAANALYSIS; PROPORTIONAL-HAZARDS; LIKELIHOOD-ESTIMATION; FRAILTY MODELS; CLUSTERED DATA; REGRESSION; HETEROGENEITY; LEVEL;
D O I
10.1002/sim.6191
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multilevel mixed effects survival models are used in the analysis of clustered survival data, such as repeated events, multicenter clinical trials, and individual participant data (IPD) meta-analyses, to investigate heterogeneity in baseline risk and covariate effects. In this paper, we extend parametric frailty models including the exponential, Weibull and Gompertz proportional hazards (PH) models and the log logistic, log normal, and generalized gamma accelerated failure time models to allow any number of normally distributed random effects. Furthermore, we extend the flexible parametric survival model of Royston and Parmar, modeled on the log-cumulative hazard scale using restricted cubic splines, to include random effects while also allowing for non-PH (time-dependent effects). Maximum likelihood is used to estimate the models utilizing adaptive or nonadaptive Gauss-Hermite quadrature. The methods are evaluated through simulation studies representing clinically plausible scenarios of a multicenter trial and IPD meta-analysis, showing good performance of the estimation method. The flexible parametric mixed effects model is illustrated using a dataset of patients with kidney disease and repeated times to infection and an IPD meta-analysis of prognostic factor studies in patients with breast cancer. User-friendly Stata software is provided to implement the methods. Copyright (C) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:3844 / 3858
页数:15
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