Biphasic testing protocols with a sub-100% sensitive primary test to detect asymptomatic disease are widely used in decision-making and testing scenarios. In this setting, a positive primary test cannot confirm the presence of the disease but triggers a confirmatory sequence that accelerates detection. In our cancer screening scenario, these latent states may be detected at some later stage, without any primary testing. We propose a model using eventual detection times of cancer to predict the prevalence of the latent state of interest. We begin by describing a model for predicting latent state prevalence in the initial screening round. The model takes into account the accelerated detection due to screening. Then, we generalize the approach into a sequence of screening rounds using a discrete-time hidden Markov model, where the emission is multivariate with time-to-event component. The model is fitted within the Bayesian framework and provides a foundation for developing risk-based targeted protocols for decision-makers. We assess estimation performance through a simulation study using two different estimation algorithms. Finally, the model is fitted to the data from a Finnish colorectal cancer screening pilot study to generate metrics for improving screening programmes.
No takes yet. Share an insight, caveat, or question.
Nevala et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: