Flexible Bayesian Survival Modeling with Semiparametric Time-Dependent and Shape-Restricted Covariate Effects
被引:14
作者:
Murray, Thomas A.
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Univ Texas MD Anderson Canc Ctr, Dept Biostat, Unit 1411, POB 301402, Houston, TX 77230 USAUniv Texas MD Anderson Canc Ctr, Dept Biostat, Unit 1411, POB 301402, Houston, TX 77230 USA
Murray, Thomas A.
[1
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Hobbs, Brian P.
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机构:
Univ Texas MD Anderson Canc Ctr, Dept Biostat, Unit 1411, POB 301402, Houston, TX 77230 USAUniv Texas MD Anderson Canc Ctr, Dept Biostat, Unit 1411, POB 301402, Houston, TX 77230 USA
Hobbs, Brian P.
[1
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Sargent, Daniel J.
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Mayo Clin, Ctr Canc, 200 First St SW, Rochester, MN 55905 USAUniv Texas MD Anderson Canc Ctr, Dept Biostat, Unit 1411, POB 301402, Houston, TX 77230 USA
Sargent, Daniel J.
[2
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Carlin, Bradley P.
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Univ Minnesota, Sch Publ Hlth, Div Biostat, Mayo Mail Code 303, Minneapolis, MN 55455 USAUniv Texas MD Anderson Canc Ctr, Dept Biostat, Unit 1411, POB 301402, Houston, TX 77230 USA
Carlin, Bradley P.
[3
]
机构:
[1] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Unit 1411, POB 301402, Houston, TX 77230 USA
[2] Mayo Clin, Ctr Canc, 200 First St SW, Rochester, MN 55905 USA
[3] Univ Minnesota, Sch Publ Hlth, Div Biostat, Mayo Mail Code 303, Minneapolis, MN 55455 USA
Presently, there are few options with available software to perform a fully Bayesian analysis of time-to-event data wherein the hazard is estimated semi-or non-parametrically. One option is the piecewise exponential model, which requires an often unrealistic assumption that the hazard is piecewise constant over time. The primary aim of this paper is to construct a tractable semiparametric alternative to the piecewise exponential model that assumes the hazard is continuous, and to provide modifiable, user-friendly software that allows the use of these methods in a variety of settings. To accomplish this aim, we use a novel model formulation for the log-hazard based on a low-rank thin plate linear spline that readily facilitates adjustment for covariates with time-dependent and proportional hazards effects, possibly subject to shape restrictions. We investigate the performance of our model choices via simulation. We then analyze colorectal cancer data from a clinical trial comparing the effectiveness of two novel treatment regimes relative to the standard of care for overall survival. We estimate a time-dependent hazard ratio for each novel regime relative to the standard of care while adjusting for the effect of aspartate transaminase, a biomarker of liver function, that is subject to a non-decreasing shape restriction.