Cost-Effectiveness Analysis of LUNGFLAGTM Risk Prediction Model in the Selection of Individuals for Lung Cancer Screening in Spain
Author(s)
Pajares V1, Soriano JB2, Seijo LM3, Trujillo JC1, Marzo M4, Olmedo-García ME5, Higuera O6, Arrabal N7, Flores A7, García JF7, Carcedo D8, Crespo M9, Heuser C10, Olghi N11, Choman E12, Gorospe L5
1Hospital de la Santa Creu i Sant Pau, Barcelona, Spain, 2Hospital Universitario La Princesa, Madrid, Spain, 3Clínica Universidad de Navarra and Ciberes, Madrid, Spain, 4Grupo de Investigación del Cáncer en Atención Primaria, Barcelona, Spain, 5Hospital Universitario Ramón y Cajal, Madrid, Spain, 6Hospital Universitario La Paz, Madrid, Spain, 7Roche Farma S.A., Madrid, Spain, 8Hygeia Consulting, Madrid, M, Spain, 9Hygeia Consulting, Madrid, Spain, 10Hoffman-la Roche, Neuenburg am Rhein, BW, Germany, 11Hoffman-la Roche, Basel, Switzerland, 12Medial Early-Sign, Hod Hasharon, Israel
Presentation Documents
OBJECTIVES: LungFlagTM is an A.I. risk prediction model that has proved to be effective in the selection of individuals for non-small cell lung cancer (NSCLC) screening. The aim of this analysis was to assess the cost-effectiveness of implementing LungFlagTM for the selection of individuals at-risk for enrollment in NSCLC screening programs in Spain.
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 of the model. A hypothetical cohort of 3.835.128 individuals who met 2013 USPSTF criteria in Spain was defined as the target population. Screening with LungFlagTM was compared to screening the whole population with no risk model and versus no-screening (current situation). Sensitivity and specificity values for LungFlagTM were obtained from Gould et al. (2021). Adherence to screening programs was assumed to be the same for both screening scenarios. A lifetime horizon was used, so a 3% discount rate was applied for both cost and effects. Only direct medical costs were considered (€2023). Sensitivity analyses were performed to assess uncertainty.
RESULTS: Using LungFlagTM to identify subjects at risk would result in 232,120 low-dose computed topographies (LDCTs) performed, compared to 2,1M of LDCTs if the whole target population was screened. Therefore, significant cost savings were obtained over the lifetime horizon (€-7,04M). However, this would mean fewer quality-adjusted life-years (QALYs) gained (-97,612 QALYs) because of fewer people screened. The incremental cost-utility ratio obtained showed that the savings generated by LungFlagTM offset the loss of QALYs, making it a cost-effective strategy. Both screening scenarios (using LungFlagTM or screening the whole target population) were dominant compared to no-screening.
CONCLUSIONS: Using LungFlagTM for the selection of individuals at-risk of NSCLC may be a cost-effective strategy compared to screening all individuals meeting USPSTF 2013 criteria or no-screening.
Conference/Value in Health Info
Value in Health, Volume 26, Issue 11, S2 (December 2023)
Code
EE74
Topic
Economic Evaluation, Medical Technologies
Topic Subcategory
Cost-comparison, Effectiveness, Utility, Benefit Analysis, Diagnostics & Imaging
Disease
No Additional Disease & Conditions/Specialized Treatment Areas, Oncology