Abstract 1737P
Background
Lung cancer screening programs using low dose computed tomography (LDCT) reduce mortality by early detection. LungFlag is an artificial intelligence-based predictive model of non-small cell lung cancer (NSCLC) risk, evaluating routine clinical and laboratory data to improve selection of individuals at-risk for enrollment in screening programs. The aim of this analysis was to assess the cost-effectiveness of LungFlag in the area of a Spanish reference center.
Methods
A combination of a decision tree and a Markov model was adapted to the Spanish setting. A multidisciplinary group of experts validated all the parameters and assumptions used in the model. Demographic characteristics were in line with those reported by Gould et al. (2021) . We defined 2 hypothetical cohorts, a broader cohort of 3000 ever-smokers aged 55-80 years, and another cohort of 1000 individuals meeting 2013 USPSTF criteria. A lifetime horizon was used, and only direct medical costs were considered. Sensitivity and specificity values were obtained from Gould et al. (2021) , and unit costs were obtained from local databases (€ 2023). Results were expressed in life-years (LYs), quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratio (ICER). Sensitivity analyses were performed to assess the consistency of the model results.
Results
LungFlag provides a higher number of LYs and QALYs with a lower cost (dominant) compared to non-screening, as shown in the table. Sensitivity analyses confirmed the robustness of base case results.
Table: 1737P
Results for the hypothetical cohorts
LungFlag | Non-screening | LungFlag vs non- screening | ||||
EvSm (n=3.000) | USPSTF (n=1.000) | EvSm (n=3.000) | USPSTF (n=1.000) | EvSm (n=3.000) | USPSTF (n=1.000) | |
LYs | 67.402 | 62.321 | 66.702 | 61.552 | +700 | +769 |
QALYs | 59.244 | 53.753 | 58.875 | 53.316 | +369 | +437 |
Total cost | 5.752.233€ | 7.584.866€ | 9.291.237€ | 12.154.655€ | -3.539.015€ | -4.569.799€ |
ICER (€ / QALY gained) | dominant | dominant |
Conclusions
The implementation of LungFlag as a risk model for NSCLC screening in a Spanish reference center would be cost-effective compared to no screening for the 2 hypothetical cohorts analyzed, providing savings and a higher clinical benefit.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Roche Pharma Spain.
Funding
Roche Pharma.
Disclosure
N. Arrabal: Other, Institutional, Advisory Board, Roche Employee: Roche Pharma. A. Flores, F. Garcia Verdes-Montenegro: Other, Institutional, Other, Roche Employee: Roche Pharma. M. Crespo, D. Carcedo: Other, Institutional, Other, Consultant: Hygeia Consulting. C. Heuser, N. Olghi: Financial Interests, Institutional, Other, Roche Employee: Roche Pharma. All other authors have declared no conflicts of interest.
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