IPECAD modeling workshop 2023 cross-comparison challenge on cost-effectiveness models in Alzheimer's Disease

Handels, R., Herring, W. L., Kamgar, F., Aye, S., Tate, A., Green, C., Gustavsson, A., Wimo, A., Winblad, B., Sköldunger, A., +13 more...Raket, L. L., Stellick, C. B., Spackman, E., Hlávka, J., Wei, Y., Mar, J., Soto-Gordoa, M., de Kok, I., Brück, C., Anderson, R., Pemberton-Ross, P., Urbich, M. & Jönsson, L. (2025). IPECAD modeling workshop 2023 cross-comparison challenge on cost-effectiveness models in Alzheimer's Disease. Value in Health, 28(4), 497 - 510. https://doi.org/10.1016/j.jval.2024.09.006
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Decision-analytic models assessing the value of emerging Alzheimer's disease (AD) treatments are challenged by limited evidence on short-term trial outcomes and uncertainty in extrapolating long-term patient-relevant outcomes. To improve understanding and foster transparency and credibility in modeling methods, we cross-compared AD decision models in a hypothetical context of disease-modifying treatment for mild cognitive impairment (MCI) due to AD. A benchmark scenario (US setting) was used with target population MCI due to AD and a set of synthetically generated hypothetical trial efficacy estimates. Treatment costs were excluded. Model predictions (10-year horizon) were assessed and discussed during a 2-day workshop. Nine modeling groups provided model predictions. Implementation of treatment effectiveness varied across models based on trial efficacy outcome selection (CDR-SB, CDR-global, MMSE, FAQ) and analysis method (observed severity transitions, change from baseline, progression hazard ratio, or calibration to these). Predicted mean time in MCI ranged from 2.6-5.2 years for control strategy, and from 0.1-1.0 years for difference between intervention and control strategies. Predicted quality-adjusted life-year gains ranged from 0.0-0.6 and incremental costs (excluding treatment costs) from -US$66,897 to US$11,896. Trial data can be implemented in different ways across health-economic models leading to large variation in model predictions. We recommend 1) addressing the choice of outcome measure and treatment effectiveness assumptions in sensitivity analysis, 2) a standardized reporting table for model predictions, and 3) exploring the use of registries for future AD treatments measuring long-term disease progression to reduce uncertainty of extrapolating short-term trial results by health economic models.

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