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Updated: Aug 6, 2026

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An R-Based Landscape Validation of a Competing Risk Model
Published on: September 16, 2022
Quantifying uncertainty of predictions from cancer progression models
Yanren Linda Hu1, Simon Pfahler2, Andreas Lösch1
1Department for Statistical Bioinformatics, University of Regensburg, Regensburg 93053, Germany.
Bioinformatics (Oxford, England)
|July 24, 2026
Summary
We developed a Bayesian framework for Mutual Hazard Networks (MHNs) to quantify uncertainty in cancer progression models. This approach improves prediction accuracy for treatment-relevant mutations and patient risk stratification.
Area of Science:
- Computational biology
- Cancer genomics
- Statistical modeling
Background:
- Cancer progression involves accumulating genomic events.
- Mutual Hazard Networks (MHNs) model cancer dynamics for predicting mutations and patient risks.
- Current MHN analyses lack uncertainty quantification, limiting clinical application.
Purpose of the Study:
- To develop an uncertainty-aware Bayesian framework for MHNs.
- To enable reliable clinical use of cancer progression models.
- To improve prediction of treatment-relevant mutations and patient monitoring.
Main Methods:
- Implemented a Bayesian framework for MHNs using Markov Chain Monte Carlo (MCMC).
- Utilized Metropolis-Adjusted Langevin Algorithm (MALA) and simplified manifold MALA (smMALA) samplers.
- Integrated MALA and smMALA into the existing mhn Python package for posterior sampling.
Main Results:
- MALA and smMALA successfully sampled MHN posteriors, with MALA performing optimally.
- Most MHN parameters and predictions showed low posterior variance, but a subset exhibited higher variability.
- Identified a lung adenocarcinoma subgroup (STK11-, KRAS+) with high, low-variance predicted risk for STK11 mutation, correlating with poorer immunotherapy survival.
Conclusions:
- The Bayesian MHN framework provides essential uncertainty quantification for clinical decision-making.
- Uncertainty assessment reveals critical parameter and prediction variability not evident in single-model analyses.
- This method enhances risk stratification for targeted therapies and patient monitoring in cancer genomics.
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