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Background <p>Individual-level microsimulation models are essential for evaluating colorectal cancer (CRC) screening programmes to capture the heterogeneity in disease progression. To ensure regional relevance, such models require detailed natural history structures and robust calibration to population-specific data. This study presents the development of the first CRC natural history microsimulation model tailored to Northern Ireland (NI) for evaluating the NI Bowel Cancer Screening Programme (NI BCSP).</p> Method <p>The model simulates individual trajectories from adenoma onset to CRC diagnosis. Eight natural history parameters were calibrated to sex-specific CRC incidence data, initially using empirical (frequentist) calibration and Approximate Bayesian Computation (ABC) rejection, followed by the ABC-Markov Chain Monte Carlo (ABC-MCMC) algorithm. Other parameters were informed by NI-specific data sources.</p> Results <p>The frequentist and ABC rejection calibration approach’s posterior distributions informed the prior distribution for the ABC-MCMC approach. ABC-MCMC was informative, yielding 55 parameter sets, but results were constrained by limited calibration targets and parameter identifiability.</p> Conclusion <p>This is the first NI-specific CRC microsimulation model, providing a regionally tailored platform for evaluating screening strategies and supporting policy. Calibration was feasible in a data-limited context, but further refinement and additional targets are needed to improve parameter estimation.</p>

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Developing and Calibrating a Colorectal Cancer Microsimulation Model for Northern Ireland

  • 期刊论文

  • 发表日期：

    2026年1月4日

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  • Olivia Adair,
  • Ethna McFerran,
  • Mark Lawler,
  • Luuk A. van Duuren,
  • Felicity Lamrock

摘要

Background

Individual-level microsimulation models are essential for evaluating colorectal cancer (CRC) screening programmes to capture the heterogeneity in disease progression. To ensure regional relevance, such models require detailed natural history structures and robust calibration to population-specific data. This study presents the development of the first CRC natural history microsimulation model tailored to Northern Ireland (NI) for evaluating the NI Bowel Cancer Screening Programme (NI BCSP).

Method

The model simulates individual trajectories from adenoma onset to CRC diagnosis. Eight natural history parameters were calibrated to sex-specific CRC incidence data, initially using empirical (frequentist) calibration and Approximate Bayesian Computation (ABC) rejection, followed by the ABC-Markov Chain Monte Carlo (ABC-MCMC) algorithm. Other parameters were informed by NI-specific data sources.

Results

The frequentist and ABC rejection calibration approach’s posterior distributions informed the prior distribution for the ABC-MCMC approach. ABC-MCMC was informative, yielding 55 parameter sets, but results were constrained by limited calibration targets and parameter identifiability.

Conclusion

This is the first NI-specific CRC microsimulation model, providing a regionally tailored platform for evaluating screening strategies and supporting policy. Calibration was feasible in a data-limited context, but further refinement and additional targets are needed to improve parameter estimation.