EClinicalMedicine (Mar 2024)

Impact on costs and outcomes of multi-gene panel testing for advanced solid malignancies: a cost-consequence analysis using linked administrative dataResearch in context

  • Alberto Hernando-Calvo,
  • Paul Nguyen,
  • Philippe L. Bedard,
  • Kelvin K.W. Chan,
  • Ramy R. Saleh,
  • Deirdre Weymann,
  • Celeste Yu,
  • Eitan Amir,
  • Dean A. Regier,
  • Bishal Gyawali,
  • Danielle Kain,
  • Brooke Wilson,
  • Craig C. Earle,
  • Nicole Mittmann,
  • Albiruni R. Abdul Razak,
  • Wanrudee Isaranuwatchai,
  • Peter Sabatini,
  • Anna Spreafico,
  • Tracy L. Stockley,
  • Trevor J. Pugh,
  • Christine Williams,
  • Lillian L. Siu,
  • Timothy P. Hanna

Journal volume & issue
Vol. 69
p. 102443

Abstract

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Summary: Background: To date, economic analyses of tissue-based next generation sequencing genomic profiling (NGS) for advanced solid tumors have typically required models with assumptions, with little real-world evidence on overall survival (OS), clinical trial enrollment or end-of-life quality of care. Methods: Cost consequence analysis of NGS testing (555 or 161-gene panels) for advanced solid tumors through the OCTANE clinical trial (NCT02906943). This is a longitudinal, propensity score-matched retrospective cohort study in Ontario, Canada using linked administrative data. Patients enrolled in OCTANE at Princess Margaret Cancer Centre from August 2016 until March 2019 were matched with contemporary patients without large gene panel testing from across Ontario not enrolled in OCTANE. Patients were matched according to 19 patient, disease and treatment variables. Full 2-year follow-up data was available. Sensitivity analyses considered alternative matched cohorts. Main Outcomes were mean per capita costs (2019 Canadian dollars) from a public payer's perspective, OS, clinical trial enrollment and end-of-life quality metrics. Findings: There were 782 OCTANE patients with 782 matched controls. Variables were balanced after matching (standardized difference 0.40), and greater in two (ovary, biliary, both p < 0.05). OCTANE was associated with greater clinical trial enrollment (25.4% vs. 9.5%, p < 0.001) and better end-of-life quality due to less death in hospital (10.2% vs. 16.4%, p = 0.003). Results were robust in sensitivity analysis. Interpretation: We found an increase in healthcare costs associated with multi-gene panel testing for advanced cancer treatment. The impact on OS was not significant, but varied across tumor types. OCTANE was associated with greater trial enrollment, lower publicly funded drug costs and fewer in-hospital deaths suggesting important considerations in determining the value of NGS panel testing for advanced cancers. Funding: T.P H holds a research grant provided by the Ontario Institute for Cancer Research through funding provided by the Government of Ontario (#IA-035 and P.HSR.158) and through funding of the Canadian Network for Learning Healthcare Systems and Cost-Effective ‘Omics Innovation (CLEO) via Genome Canada (G05CHS).

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