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Checkmate 9la clinical study
Checkmate 9la clinical study





checkmate 9la clinical study

None of the included studies fulfilled all of the criteria reported in the Philips and the CHEC checklists. Our systematic review and methodology assessment revealed that the methods of estimation of long-term outcomes, quantification of health state utility values, estimation of drug costs, the accuracy of data sources, and their credibility have important implications on the cost-effectiveness outcomes. Quality assessment of the included studies highlighted shortcomings in data identification, uncertainty assessment, and methods transparency. Cost-effectiveness analyses differed substantially due to the applied modeling methods, sources of costs, health state utilities, and key assumptions. Seven studies met the inclusion criteria. The methodological quality of the included studies was assessed by the Philips checklist and the Consensus Health Economic Criteria (CHEC) checklist. PubMed, Embase, and the Cost-Effectiveness Analysis Registry were searched, in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. To assess the methodological quality of cost-effectiveness analyses (CEA) of nivolumab in combination with ipilimumab, we conducted a systematic literature review in the first-line treatment of patients with recurrent or metastatic non-small cell lung cancer (NSCLC), whose tumors express programmed death ligand-1, with no epidermal growth factor receptor or anaplastic lymphoma kinase genomic tumor aberrations. Erasmus School of Health Policy & Management, Erasmus University Rotterdam, Rotterdam, Netherlands.







Checkmate 9la clinical study