scholarly journals Goodness-of-Fit Tests for Censored Survival Data

1985 ◽  
Vol 13 (2) ◽  
pp. 552-563 ◽  
Author(s):  
Robert J. Gray ◽  
Donald A. Pierce
2017 ◽  
Author(s):  
Michael Holton Price ◽  
James Holland Jones

AbstractExisting goodness-of-fit tests for survival data are either exclusively graphical in nature or only test specific model assumptions, such as the proportional hazards assumption. We describe a flexible, parameter-free goodness-of-fit test that provides a simple numerical assessment of a model’s suitability regardless of the structure of the underlying model. Intuitively, the goodness-of-fit test utilizes the fact that for a good model early event occurrence is predicted to be just as likely as late event occurrence, whereas a bad model has a bias towards early or late events. Formally, the goodness-of-fit test is based on a novel generalized Martingale residual which we call the martingale survival residual. The martingale survival residual has a uniform probability density function defined on the interval −0.5 to +0.5 if censoring is either absent or accounted for as one outcome in a competing hazards framework. For a good model, the set of calculated residuals is statistically indistinguishable from the uniform distribution, which is tested using the Kolmogorov-Smirnov statistic.


2011 ◽  
Vol 150 (3) ◽  
pp. 319-334 ◽  
Author(s):  
L. D. B. SURIYAGODA ◽  
M. H. RYAN ◽  
H. LAMBERS ◽  
M. RENTON

SUMMARYThe present paper compares standard and novel methods for analysing aggregated patterns of plant death in designed field experiments; these methods include binomial (BN), beta-binomial (BBN), logistic-normal-binomial (LNB), BN models with random blocks, BN models with smooth-scale spatial components and principal coordinates of neighbour matrices (PCNM). PCNM is a relatively new technique used in ecology to determine how much observed variability can be explained by spatial and environmental variables, and has not yet been applied to agricultural studies. The survival data of two pasture species, collected from a designed field experiment that was replicated at multiple locations, were used. First, the occurrence of overdispersion was tested using the BN and BBN distributions. Goodness-of-fit tests proved that the BBN model provided a better description (better fit) of the observed data in some cases than did the BN distribution, indicating overdispersion was present. When overdispersion was not present, the BN distribution was adequate to describe the data, and the use of the BBN distribution was superfluous. It is then shown that the PCNM approach, the BN model with smooth-scale spatial components and the LNB model were able to account for some of the variation as spatial variability, thus reducing the species effect compared with that explained under the standard BN model. The amount of variation among species according to the BN model and the BN model with random blocks was similar. Therefore, it is argued that the novel PCNM approach warrants further testing when exploring the spatial variability in designed experiments in agriculture and using LNB, PCNM and BN with smooth-scale spatial components may provide better predictions of species effects than do other, more conventional, approaches.


2016 ◽  
Vol 27 (7) ◽  
pp. 2114-2131 ◽  
Author(s):  
Sylvie Scolas ◽  
Catherine Legrand ◽  
Abderrahim Oulhaj ◽  
Anouar El Ghouch

Models for interval-censored survival data presenting a fraction of “cure” or “immune” patients have recently been proposed in the literature, particularly extending the mixture cure model to interval-censored data. However, little is known about the goodness-of-fit of such models. In a mixture cure model, the survival distribution of the entire population is improper and expressed in terms of the survival distribution of uncured individuals, i.e. the latency part of the model, and the probability to experience the event of interest, i.e. the incidence part. To validate a mixture cure model, assumptions made on both parts need to be checked, i.e. the survival distribution of uncured individuals, the link function used in the latency and the linearity of the covariates used in the both parts of the model. In this work, we investigate the Cox-Snell and deviance residuals and show how they can be adapted and used to perform diagnostics checks when all subjects are right- or interval-censored and some subjects are cured with unknown cure status. A large simulation study investigates the ability of these residuals to detect a departure from the assumptions of the mixture model. Developed techniques are applied to a real data set about Alzheimer’s disease.


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