Browse
Submit Data
Databases
API
Help

Dataset Information

32 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Accelerated failure time model under general biased sampling scheme.

ABSTRACT: Right-censored time-to-event data are sometimes observed from a (sub)cohort of patients whose survival times can be subject to outcome-dependent sampling schemes. In this paper, we propose a unified estimation method for semiparametric accelerated failure time models under general biased estimating schemes. The proposed estimator of the regression covariates is developed upon a bias-offsetting weighting scheme and is proved to be consistent and asymptotically normally distributed. Large sample properties for the estimator are also derived. Using rank-based monotone estimating functions for the regression parameters, we find that the estimating equations can be easily solved via convex optimization. The methods are confirmed through simulations and illustrated by application to real datasets on various sampling schemes including length-bias sampling, the case-cohort design and its variants.

SUBMITTER: Kim JP

PROVIDER: S-EPMC5006413 | biostudies-literature | 2016 Jul

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Accelerated failure time model under general biased sampling scheme.

Kim Jane Paik JP Sit Tony T Ying Zhiliang Z

Biostatistics (Oxford, England) 20160303 3

Right-censored time-to-event data are sometimes observed from a (sub)cohort of patients whose survival times can be subject to outcome-dependent sampling schemes. In this paper, we propose a unified estimation method for semiparametric accelerated failure time models under general biased estimating schemes. The proposed estimator of the regression covariates is developed upon a bias-offsetting weighting scheme and is proved to be consistent and asymptotically normally distributed. Large sample p ...[more]

PMID: 26941240

Similar Datasets

Efficient estimation for accelerated failure time model under case-cohort and nested case-control sampling.

Project description:Case-cohort (Prentice, 1986) and nested case-control (Thomas, 1977) designs have been widely used as a cost-effective alternative to the full-cohort design. In this article, we propose an efficient likelihood-based estimation method for the accelerated failure time model under case-cohort and nested case-control designs. An EM algorithm is developed to maximize the likelihood function and a kernel smoothing technique is adopted to facilitate the estimation in the M-step of the EM algorithm. We show that the proposed estimators for the regression coefficients are consistent and asymptotically normal. The asymptotic variance of the estimators can be consistently estimated using an EM-aided numerical differentiation method. Simulation studies are conducted to evaluate the finite-sample performance of the estimators and an application to a Wilms tumor data set is also given to illustrate the methodology.

| S-EPMC5288392 | biostudies-literature

Accelerated failure time model for data from outcome-dependent sampling.

Project description:Outcome-dependent sampling designs such as the case-control or case-cohort design are widely used in epidemiological studies for their outstanding cost-effectiveness. In this article, we propose and develop a smoothed weighted Gehan estimating equation approach for inference in an accelerated failure time model under a general failure time outcome-dependent sampling scheme. The proposed estimating equation is continuously differentiable and can be solved by the standard numerical methods. In addition to developing asymptotic properties of the proposed estimator, we also propose and investigate a new optimal power-based subsamples allocation criteria in the proposed design by maximizing the power function of a significant test. Simulation results show that the proposed estimator is more efficient than other existing competing estimators and the optimal power-based subsamples allocation will provide an ODS design that yield improved power for the test of exposure effect. We illustrate the proposed method with a data set from the Norwegian Mother and Child Cohort Study to evaluate the relationship between exposure to perfluoroalkyl substances and women's subfecundity.

| S-EPMC7856009 | biostudies-literature

Mediation Analysis for Censored Survival Data Under an Accelerated Failure Time Model.

Project description:Recent advances in causal mediation analysis have formalized conditions for estimating direct and indirect effects in various contexts. These approaches have been extended to a number of models for survival outcomes including accelerated failure time models, which are widely used in a broad range of health applications given their intuitive interpretation. In this setting, it has been suggested that under standard assumptions, the "difference" and "product" methods produce equivalent estimates of the indirect effect of exposure on the survival outcome. We formally show that these two methods may produce substantially different estimates in the presence of censoring or truncation, due to a form of model misspecification. Specifically, we establish that while the product method remains valid under standard assumptions in the presence of independent censoring, the difference method can be biased in the presence of such censoring whenever the error distribution of the accelerated failure time model fails to be collapsible upon marginalizing over the mediator. This will invariably be the case for most choices of mediator and outcome error distributions. A notable exception arises in case of normal mediator-normal outcome where we show consistency of both difference and product estimators in the presence of independent censoring. These results are confirmed in simulation studies and two data applications.

| S-EPMC5756668 | biostudies-literature

Analyzing Length-biased Data with Semiparametric Transformation and Accelerated Failure Time Models.

Project description:Right-censored time-to-event data are often observed from a cohort of prevalent cases that are subject to length-biased sampling. Informative right censoring of data from the prevalent cohort within the population often makes it difficult to model risk factors on the unbiased failure times for the general population, because the observed failure times are length biased. In this paper, we consider two classes of flexible semiparametric models: the transformation models and the accelerated failure time models, to assess covariate effects on the population failure times by modeling the length-biased times. We develop unbiased estimating equation approaches to obtain the consistent estimators of the regression coefficients. Large sample properties for the estimators are derived. The methods are confirmed through simulations and illustrated by application to data from a study of a prevalent cohort of dementia patients.

| S-EPMC2972554 | biostudies-literature

Regularized estimation for the accelerated failure time model.

Project description:In the presence of high-dimensional predictors, it is challenging to develop reliable regression models that can be used to accurately predict future outcomes. Further complications arise when the outcome of interest is an event time, which is often not fully observed due to censoring. In this article, we develop robust prediction models for event time outcomes by regularizing the Gehan's estimator for the accelerated failure time (AFT) model (Tsiatis, 1996, Annals of Statistics 18, 305-328) with least absolute shrinkage and selection operator (LASSO) penalty. Unlike existing methods based on the inverse probability weighting and the Buckley and James estimator (Buckley and James, 1979, Biometrika 66, 429-436), the proposed approach does not require additional assumptions about the censoring and always yields a solution that is convergent. Furthermore, the proposed estimator leads to a stable regression model for prediction even if the AFT model fails to hold. To facilitate the adaptive selection of the tuning parameter, we detail an efficient numerical algorithm for obtaining the entire regularization path. The proposed procedures are applied to a breast cancer dataset to derive a reliable regression model for predicting patient survival based on a set of clinical prognostic factors and gene signatures. Finite sample performances of the procedures are evaluated through a simulation study.

| S-EPMC3073158 | biostudies-literature

LOCAL BUCKLEY-JAMES ESTIMATION FOR HETEROSCEDASTIC ACCELERATED FAILURE TIME MODEL.

Project description:In survival analysis, the accelerated failure time model is a useful alternative to the popular Cox proportional hazards model due to its easy interpretation. Current estimation methods for the accelerated failure time model mostly assume independent and identically distributed random errors, but in many applications the conditional variance of log survival times depend on covariates exhibiting some form of heteroscedasticity. In this paper, we develop a local Buckley-James estimator for the accelerated failure time model with heteroscedastic errors. We establish the consistency and asymptotic normality of the proposed estimator and propose a resampling approach for inference. Simulations demonstrate that the proposed method is flexible and leads to more efficient estimation when heteroscedasticity is present. The value of the proposed method is further assessed by the analysis of a breast cancer data set.

| S-EPMC4988529 | biostudies-literature

Generalized accelerated failure time spatial frailty model for arbitrarily censored data.

Project description:Flexible incorporation of both geographical patterning and risk effects in cancer survival models is becoming increasingly important, due in part to the recent availability of large cancer registries. Most spatial survival models stochastically order survival curves from different subpopulations. However, it is common for survival curves from two subpopulations to cross in epidemiological cancer studies and thus interpretable standard survival models can not be used without some modification. Common fixes are the inclusion of time-varying regression effects in the proportional hazards model or fully nonparametric modeling, either of which destroys any easy interpretability from the fitted model. To address this issue, we develop a generalized accelerated failure time model which allows stratification on continuous or categorical covariates, as well as providing per-variable tests for whether stratification is necessary via novel approximate Bayes factors. The model is interpretable in terms of how median survival changes and is able to capture crossing survival curves in the presence of spatial correlation. A detailed Markov chain Monte Carlo algorithm is presented for posterior inference and a freely available function frailtyGAFT is provided to fit the model in the R package spBayesSurv. We apply our approach to a subset of the prostate cancer data gathered for Louisiana by the surveillance, epidemiology, and end results program of the National Cancer Institute.

| S-EPMC5352560 | biostudies-literature

Dimension reduction of microarray gene expression data: the accelerated failure time model.

Project description:The construction of the components of Partial Least Squares (PLS) is based on the maximization of the covariance/correlation between linear combinations of the predictors and the response. However, the usual Pearson correlation is influenced by outliers in the response or in the predictors. To cope with outliers, we replace the Pearson correlation with the Spearman rank correlation in the optimization criteria of PLS. The rank-based method of PLS is insensitive to outlying values in both the predictors and response, and incorporates the censoring information by using an approach of Nguyen and Rocke (2004) and two approaches of reweighting and mean imputation of Datta et al. (2007). The performance of the rank-based approaches of PLS, denoted by Rank-based Modified Partial Least Squares (RMPLS), Rank-based Reweighted Partial Least Squares (RRWPLS), and Rank-based Mean-Imputation Partial Least Squares (RMIPLS), is investigated in a simulation study and on four real datasets, under an Accelerated Failure Time (AFT) model, against their un-ranked counterparts, and several other dimension reduction techniques. The results indicate that RMPLS is a better dimension reduction method than other variants of PLS as well as other considered methods in terms of the minimized cross-validation error of fit and the mean squared error of fit in the presence of outliers in the response, and is comparable to other variants of PLS in the absence of outliers. Supplementary Materials are available at http://www.worldscinet.com/jbcb/

| S-EPMC2796584 | biostudies-literature

EFFICIENT ESTIMATION FOR AN ACCELERATED FAILURE TIME MODEL WITH A CURE FRACTION.

Project description:We study the accelerated failure time model with a cure fraction via kernel-based nonparametric maximum likelihood estimation. An EM algorithm is developed to calculate the estimates for both the regression parameters and the unknown error density, in which a kernel-smoothed conditional profile likelihood is maximized in the M-step. We show that with a proper choice of the kernel bandwidth parameter, the resulting estimates are consistent and asymptotically normal. The asymptotic covariance matrix can be consistently estimated by inverting the empirical Fisher information matrix obtained from the profile likelihood using the EM algorithm. Numerical examples are used to illustrate the finite-sample performance of the proposed estimates.

| S-EPMC2857521 | biostudies-literature

Variable selection in the accelerated failure time model via the bridge method.

Project description:In high throughput genomic studies, an important goal is to identify a small number of genomic markers that are associated with development and progression of diseases. A representative example is microarray prognostic studies, where the goal is to identify genes whose expressions are associated with disease free or overall survival. Because of the high dimensionality of gene expression data, standard survival analysis techniques cannot be directly applied. In addition, among the thousands of genes surveyed, only a subset are disease-associated. Gene selection is needed along with estimation. In this article, we model the relationship between gene expressions and survival using the accelerated failure time (AFT) models. We use the bridge penalization for regularized estimation and gene selection. An efficient iterative computational algorithm is proposed. Tuning parameters are selected using V-fold cross validation. We use a resampling method to evaluate the prediction performance of bridge estimator and the relative stability of identified genes. We show that the proposed bridge estimator is selection consistent under appropriate conditions. Analysis of two lymphoma prognostic studies suggests that the bridge estimator can identify a small number of genes and can have better prediction performance than the Lasso.

| S-EPMC2989175 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data