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Understanding Bladder Cancer Screening Limits Through Comparative Modeling: The Maximum Clinical Incidence Reduction
Medrxiv : the Preprint Server for Health Sciences
|February 6, 2026
Summary
Bladder cancer screening effectiveness is limited by a short detectable preclinical phase, according to three models. Findings suggest focusing on risk-targeted and repeated screening strategies for better bladder cancer detection.
Area of Science:
- Oncology
- Epidemiology
- Health Economics
Background:
- Bladder cancer presents significant clinical and economic challenges.
- Key natural history parameters for screening effectiveness, like preclinical reservoir size and sojourn time, are difficult to observe.
- The Cancer Intervention and Surveillance Modeling Network (CISNET) uses standardized stress tests to compare microsimulation models and understand intervention impacts.
Purpose of the Study:
- To compare three independently developed bladder cancer microsimulation models using the CISNET Maximum Clinical Incidence Reduction (MCLIR) and Realistic Clinical Incidence Reduction (RCLIR) frameworks.
- To assess the impact of one-time screening interventions on bladder cancer incidence reduction.
- To understand how model differences influence predictions of screening effectiveness.
Main Methods:
- Applied the CISNET MCLIR/RCLIR protocol to three models (COBRAS, Kystis, SCOUT) calibrated to U.S. epidemiologic targets.
- Simulated a 1950 U.S. birth cohort under no-screening, perfect screening (MCLIR), and realistic screening (RCLIR-1 and RCLIR-2) scenarios.
- Analyzed age-specific clinical incidence, incidence-reduction curves, and cumulative reductions.
Main Results:
- Median preclinical sojourn times varied across models (2.1 to 3.3 years).
- Peak incidence reductions under MCLIR ranged from 20% to 32% at age 65 for White men, with varying persistence.
- Realistic screening (RCLIR) yielded smaller reductions, and most residual incidence was due to new lesion emergence.
Conclusions:
- Three bladder cancer microsimulation models suggest a short detectable preclinical phase, limiting one-time screening effectiveness.
- Differences in model predictions are linked to variations in implied sojourn time and detectable reservoir size.
- Findings support evaluating risk-targeted and repeated screening, and identify priorities for improving bladder cancer natural history inference.
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