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.
Resources from the same session
1902P - Comparison of cabozantinib (CABO) versus sunitinib (SUN) following first-line (1L) nivolumab plus ipilimumab (NIVO+IPI) for metastatic renal cell carcinoma (mRCC): A target trial emulation using real-world data from the International mRCC Database Consortium (IMDC)
Presenter: Audreylie Lemelin
Session: Poster session 23
1903P - Tumor response by baseline metastases in patients (pts) with renal cell carcinoma (RCC) treated with lenvatinib (L) plus pembrolizumab (P) vs sunitinib (S): Post hoc analysis of the CLEAR trial
Presenter: Viktor Gruenwald
Session: Poster session 23
1904P - Treatment options and outcome of metastatic renal cell carcinoma patients with brain or bone metastases: A real-world evidence from a German retrospective multi-center analysis
Presenter: Pia Paffenholz
Session: Poster session 23
1905P - Heterogeneity in tertiary lymphoid structures predicts the distinct prognosis and immune microenvironment of clear cell renal cell carcinoma
Presenter: Wenhao Xu
Session: Poster session 23
1906P - Metastasized non-clear cell renal cell carcinoma: Which entities are dangerous? Results learned from reference pathology of the SuniForecast study
Presenter: Arndt Hartmann
Session: Poster session 23
1907P - Multi-omics mapping positions antigenic myeloid-T cell crosstalk at the core of advanced renal cell carcinoma (aRCC) response to immune checkpoint blockade (ICB)
Presenter: Lisa Kinget
Session: Poster session 23
1908P - Utility of circulating tumor (ct)DNA testing for molecular residual disease (MRD) detection and treatment response monitoring in patients (pts) with renal cell carcinoma (RCC)
Presenter: Michael Smigelski
Session: Poster session 23
1909P - Baseline cytokine levels according to the line of treatment in patients with metastatic clear cell renal cell carcinoma treated with nivolumab: NIVOREN GETUG-AFU 26 translational study
Presenter: Larissa Rainho
Session: Poster session 23
1910P - Evaluation of a genome-wide methylome enrichment platform for circulating tumor DNA quantification and prognostic performance in renal cell carcinoma (RCC)
Presenter: Brian Rini
Session: Poster session 23
1911P - Effect of VHL mutations on efficacy of immune checkpoint inhibitors in renal cell carcinoma
Presenter: Guojie Yu
Session: Poster session 23