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Clinical and economic impact of 'ROS1-testing' strategy compared to a 'no-ROS1-testing' strategy in advanced NSCLC in Spain.

dc.contributor.authorRojo, Federico
dc.contributor.authorConde, Esther
dc.contributor.authorTorres, Héctor
dc.contributor.authorCabezón-Gutiérrez, Luis
dc.contributor.authorBautista, Dolores
dc.contributor.authorRamos, Inmaculada
dc.contributor.authorCarcedo, David
dc.contributor.authorArrabal, Natalia
dc.contributor.authorGarcía, J Francisco
dc.contributor.authorGalán, Raquel
dc.contributor.authorNadal, Ernest
dc.date.accessioned2023-05-03T13:33:22Z
dc.date.available2023-05-03T13:33:22Z
dc.date.issued2022-03-19
dc.description.abstractDetection of the ROS1 rearrangement is mandatory in patients with advanced or metastatic non-small cell lung cancer (NSCLC) to allow targeted therapy with specific inhibitors. However, in Spanish clinical practice ROS1 determination is not yet fully widespread. The aim of this study is to determine the clinical and economic impact of sequentially testing ROS1 in addition to EGFR and ALK in Spain. A joint model (decision-tree and Markov model) was developed to determine the cost-effectiveness of testing ROS1 strategy versus a no-ROS1 testing strategy in Spain. Distribution of ROS1 techniques, rates of testing, positivity, and invalidity of biomarkers included in the analysis (EGFR, ALK, ROS1 and PD-L1) were based on expert opinion and Lungpath real-world database. Treatment allocation depending on the molecular testing results was defined by expert opinion. For each treatment, a 3-states Markov model was developed, where progression-free survival (PFS) and overall survival (OS) curves were parameterized using exponential extrapolations to model transition of patients among health states. Only medical direct costs were included (€ 2021). A lifetime horizon was considered and a discount rate of 3% was applied for both costs and effects. Both deterministic and probabilistic sensitivity analyses were performed to address uncertainty. A target population of 8755 patients with advanced NSCLC (non-squamous or never smokers squamous) entered the model. Over a lifetime horizon, the ROS1 testing scenario produced additional 157.5 life years and 121.3 quality-adjusted life years (QALYs) compared with no-ROS1 testing scenario. Total direct costs were increased up to € 2,244,737 for ROS1 testing scenario. The incremental cost-utility ratio (ICUR) was 18,514 €/QALY. Robustness of the base-case results were confirmed by the sensitivity analysis. Our study shows that ROS1 testing in addition to EGFR and ALK is a cost-effective strategy compared to no-ROS1 testing, and it generates more than 120 QALYs in Spain over a lifetime horizon. Despite the low prevalence of ROS1 rearrangements in NSCLC patients, the clinical and economic consequences of ROS1 testing should encourage centers to test all advanced or metastatic NSCLC (non-squamous and never-smoker squamous) patients.
dc.identifier.doi10.1186/s12885-022-09397-4
dc.identifier.essn1471-2407
dc.identifier.pmcPMC8933896
dc.identifier.pmid35303812
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933896/pdf
dc.identifier.unpaywallURLhttps://bmccancer.biomedcentral.com/track/pdf/10.1186/s12885-022-09397-4
dc.identifier.urihttp://hdl.handle.net/10668/20278
dc.issue.number1
dc.journal.titleBMC cancer
dc.journal.titleabbreviationBMC Cancer
dc.language.isoen
dc.organizationHospital Universitario Virgen de la Victoria
dc.organizationHospital Costa del Sol
dc.page.number292
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBiomarker guided selection
dc.subjectC-ros oncogene 1
dc.subjectCost-effectiveness analysis
dc.subjectMolecular testing
dc.subjectNon-small cell lung cancer
dc.subject.meshBiomarkers, Tumor
dc.subject.meshBiopsy
dc.subject.meshCarcinoma, Non-Small-Cell Lung
dc.subject.meshCost-Benefit Analysis
dc.subject.meshFemale
dc.subject.meshGene Rearrangement
dc.subject.meshHumans
dc.subject.meshLung Neoplasms
dc.subject.meshMale
dc.subject.meshMolecular Diagnostic Techniques
dc.subject.meshProtein-Tyrosine Kinases
dc.subject.meshProto-Oncogene Proteins
dc.subject.meshQuality-Adjusted Life Years
dc.subject.meshSpain
dc.titleClinical and economic impact of 'ROS1-testing' strategy compared to a 'no-ROS1-testing' strategy in advanced NSCLC in Spain.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number22
dspace.entity.typePublication

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