A Bayesian Markov Framework for Modeling Breast Cancer Progression

This study develops a three-state Markov framework to estimate the transition rates between normal, preclinical screen-detectable phase (PCDP), and clinical breast cancer using simulated data. Two exponential models are explored: a five-mode transition model and a six-mode transition model, the latter incorporating exact cancer case timings. Each model is analyzed both with and without covariates to evaluate their influence on breast cancer progression. Parameters are estimated utilizing maximum likelihood estimation and Bayesian models with Gibbs sampling to ensure robustness and methodological rigor. Additionally, a nonhomogeneous model based on the Weibull distribution is introduced to account for time-varying transition rates, providing a more dynamic perspective on disease progression. While the analysis is conducted with simulated data, the framework is adaptable to real-world datasets, offering valuable insights for refining screening policies and optimizing inter-screening intervals.

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Publication Details

Journal
Mathematics
Published
2024-12-27
DOI
https://doi.org/10.3390/math13010065
Citations
1
Primary Topic
Statistical Methods and Inference
Type
article
Field-Weighted Citation Impact
0.71
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article

A Bayesian Markov Framework for Modeling Breast Cancer Progression

Tong Wu
1 citations
Mathematics
Statistical Methods and Inference
0.71
article

A Bayesian Markov Framework for Modeling Breast Cancer Progression

Tong Wu
article en
1 citations

Abstract

This study develops a three-state Markov framework to estimate the transition rates between normal, preclinical screen-detectable phase (PCDP), and clinical breast cancer using simulated data. Two exponential models are explored: a five-mode transition model and a six-mode transition model, the latter incorporating exact cancer case timings. Each model is analyzed both with and without covariates to evaluate their influence on breast cancer progression. Parameters are estimated utilizing maximum likelihood estimation and Bayesian models with Gibbs sampling to ensure robustness and methodological rigor. Additionally, a nonhomogeneous model based on the Weibull distribution is introduced to account for time-varying transition rates, providing a more dynamic perspective on disease progression. While the analysis is conducted with simulated data, the framework is adaptable to real-world datasets, offering valuable insights for refining screening policies and optimizing inter-screening intervals.

MathematicsVol. 13(1)
University of Massachusetts Boston (US)
Good health and well-being
Openalex Percentile: Top 23%
Statistical Methods and Inference
0.71
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