A Regression Model For Recurrent Events With Distribution Free Correlation Structure

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A Regression Model For Recurrent Events With Distribution Free Correlation Structure J. Pénichoux(1), A. Latouche(2), T. Moreau(1) (1) INSERM U780 (2) Université de Versailles, EA2506 ISCB - 2009 - Prague

Funding : 2008 doctoral fellowship from AXA research fund

Background Each subject i (i = 1,..., N ) can experience K i repeated occurrences of the same type of event during his follow-up. 2 issues Estimation of covariates effect on the risk of occurrence Assessment of the strength of correlation between events Motivation : On-going cohort study on the risk of recurrent infections in patients with cystic fibrosis (364 patients). Being aware of the presence of correlation can influence therapeutical decisions. Worked example : infection times for patients with chronic granulotomous disease (CGD)

Handling of recurrent events (1) Extensions of Cox proportional hazards model Timescale for a conditional model Gap time : T i (k) = T i (k) T i (k 1) Calendar time :T i (k) with T i (1),...,T i (K ) the successive event times for individual i Our framework : Gap time Handling of correlation : Stratification of the baseline hazard on the rank of event to account for event dependence Random effect (frailty) to account for heterogeneity across individuals [1] KELLY, P.J. AND LIM, L.L.(2000)Stat Med

Handling of recurrent events (2) The conditional frailty model for gap time where t = t t i (k 1) λ ik (t T i (k 1) = t i (k 1), X i ) = u i λ 0k ( t)exp( t βx i ) u i : random effect, shared for all intervals of individual i, with expectation 1 and variance ϕ (usually gamma). Accounts for heterogeneity across individuals λ 0k : interval-specific hazard to account for event dependence [1]. Some issues : The estimation of the variance of the random effect is complex assessment and estimation of correlation might not be straightforward. The history of an individual is not used to evaluate his current risk. [2] BOX-STEFFENSMEIER, J. AND DE BOEF, S. (2006)Stat Med

Proposed approach (1) Hazard of event k for individual i λ ik (t T i (k 1) = t i (k 1), X i ) = λ 0k ( t)exp θ (1 ˆΛ k 1 ( t i (k 1) )) + t }{{} βx i Z ik with t = t t i (k 1), Z ik interval-specific covariate (Z ik = 0 if k = 1), ˆΛ k 1 : cumulative hazard estimated with Breslow s formula computed on the (k 1) intervals, X i a vector of covariates for individual i Estimation of parameters θ,β : simple partial likelihood maximization.

Proposed approach (2) Interpretation of Z ik : (Z ik = 1 ˆΛ k 1 ( t i (k 1) )) Difference between 1 : the observed number of events during the previous interval [t i (k 2), t i (k 1) ] ˆΛ (k 1) ( t i (k 1) ) : the expected number of events in this interval estimated under a Poisson process with intensity λ k 1 Interpretation of parameter θ The proposed approach for two successive events is an approximation of a shared-gamma frailty model close to ϕ = 0 (ie close to the independence), with θ ϕ[1] To keep the comparability with a frailty, θ > 0 in the proposed approach ( ˆθ = max(0, ˆθ ml )). [3] LEFFONDRÉ, K., LELLOUCH, J.,COM-NOUGUÉ, C. AND MOREAU, T. (2001)Commun. Stat., Theory Methods

Simulation outline In the sequel, we ll consider : 2 events per subject, no censoring Outline Estimation of covariates effects using simulations from gamma and lognormal frailty models Estimation of the variance of the frailty using simulations from a gamma frailty model Test of independence, type I error and power using simulations from gamma frailty models Example : CGD data Models compared "PWP-GT" (Usual stratified Cox) Conditional Gamma Frailty Proposed approach

Estimation of covariates effect 500 repetitions, N = 100 β = 0.7 (RR 2) β = 1.1 (RR 3) ˆβ ˆσ β ˆβ ˆσβ PWP-GT 0.596 0.150 0.939 0.157 ϕ = 0.2 CGFM* 0.662 0.174 1.050 0.182 Gamma PA* 0.605 0.150 0.955 0.157 PWP-GT 0.446 0.147 0.730 0.150 ϕ = 0.6 CGFM* 0.664 0.231 1.071 0.235 PA* 0.484 0.148 0.793 0.153 PWP-GT 0.614 0.150 0.979 0.158 ϕ = 0.2 CGFM* 0.668 0.168 1.056 0.176 Lognormal PA* 0.623 0.151 0.990 0.158 PWP-GT 0.558 0.149 0.868 0.154 ϕ = 0.6 CGFM* 0.682 0.198 1.053 0.200 PA* 0.576 0.150 0.893 0.155 * CGFM : Conditional gamma frailty model PA : Proposed Approach [1] THERNEAU, TM. AND GRAMBSCH, PM. (2000). Modeling Survival Data : Extending the Cox Model. Springer

Estimation of the variance of the frailty Simulations : Gamma shared frailty models with variance ϕ 1000 repetitions for each value of ϕ N = 200 for each dataset Before ϕ = 0.25, ˆθ estimated by the proposed approach is closer to the variance of the frailty. After ϕ = 0.25, ˆϕ estimated by a gamma shared frailty model is closer.

Test of independence and type I error 1000 repetitions Nominal level for type I error ˆϕ ˆθ 5% 1% 1 N=50 CGFM* 1.7% 0.5% 0.1% 0.020. PA* 3.7% 0.4% 0.1%. 0.055 N=100 CGFM* 1.7% 0.4% 0.1% 0.015. PA* 3.9% 0.6% 0.0%. 0.039 N=200 CGFM* 1.9% 0.6% 0.1% 0.012. PA* 4.6% 0.9% 0.0%. 0.028 * CGFM : Conditional gamma frailty model PA : Proposed approach

Test of independence and power 1000 repetitions Power (%) CGFM* PA* CGFM* ( ˆϕ) PA* ( ˆθ) N=50 17.9 28.0 0.11 0.19 ϕ = 0.2 N=100 34.4 47.3 0.14 0.17 N=200 60.5 73.8 0.16 0.17 N=50 52.7 64.0 0.28 0.33 ϕ = 0.4 N=100 81.8 88.6 0.32 0.32 N=200 97.7 98.7 0.36 0.31 N=50 74.9 83.0 0.43 0.45 ϕ = 0.6 N=100 97.0 97.6 0.50 0.44 N=200 100 100 0.54 0.43 * CGFM : Conditional gamma frailty model PA : Proposed Approach

Application to the CGD data CGD data : Data from a placebo controlled trial examining the effect of gamma interferon in chronic granulotomous disease (CGD), which manifests in recurrent infections. 135 patients included Model β treat ˆ p-value ˆϕ ˆθ PWP-GT -0.8760 0.0016.. Conditional shared gamma fraitly model -0.8760 0.0016 0,00. Proposed approach -0.8562 0.0023. 0* * ˆθ ml = 0.5434

Conclusion Covariates effect estimation GF : robust estimation of covariates effect Assessment of correlation and test of independence Perpectives Correct Type I error for both approaches Greater power for the proposed approach Better estimation of the variance of a frailty for small datasets and small values of ϕ Easy to develop for non stratified analysis and calendar timescale Extending the analysis to non-shared frailties which would combine the two sources of correlation

Bibliography [1] P. Kelly and L. Lim, Survival analysis for recurrent event data : an application to childhood infectious diseases, Stat Med, vol. 19, pp. 13 33, Jan 2000. [2] J. Box-Steffensmeier and S. De Boef, Repeated events survival models : the conditional frailty model, Stat Med, vol. 25, pp. 3518 3533, Oct 2006. [3] K. Leffondré, J. Lellouch, C. Com-Nougué, and T. Moreau, Optimality of nonparametric tests for association between survival time and continuous covariates., Commun. Stat., Theory Methods, vol. 30, no. 5, pp. 913 929, 2001. [4] T. M. Therneau and P. M. Grambsch, Modeling survival data : extending the cox model. Statistics for biology and health, Springer, 2000.

Partial likelihood for our approach where L = ˆΛ k 1 (t) = n n i i=1 k=1 exp (t βx i + θ{1 ˆΛ k 1 (t i (k 1) )} ) n l=1 Y l (T ik )exp (t βx l + θ{1 ˆΛ k 1 (t l(k 1) )} ) T j (k 1) t l Y l (T j (k 1) )=1 δ j exp( t ˆβk 1 X l (T j (k 1) )) exp(t ˆβk 1 X )

Example of results with censorship and any number of events Modèle ˆβ Var( ˆ Stratified Cox model -0.9097 0.0610 Stratified shared gamma frailty model -0.9463 0.0657 Proposed approach -0.9271 0.0618 TAB.: Simulations under a gamma frailty, n = 50, λ 0 = 1, β = 1