Introduction: Genome sequencing (GS) and exome sequencing (ES) technologies have gained increasing attention in health economics for evaluating their clinical and public health introduction, but their complexity challenges traditional methods. This systematic review aimed to investigate and discuss full economic evaluations (EEs) of GS and ES in relation to health outcomes, with a focus on methodological issues. Methods: A systematic search of several databases was carried out (PROSPERO CRD42023430992). Quality was evaluated using the Quality of Health Economic Studies instrument. Key methodological features were investigated, and a narrative synthesis of the findings was performed after grouping studies by testing scope. Results: Overall, 12 recently published cost-utility analyses (CUAs) were included, assessing the use of GS/ES for guiding targeted therapy in oncology (N = 4) or major depressive disorder (N = 1), and diagnosing rare genetic diseases (N = 7). The findings suggested that GS/ES may be cost-effective for diagnosing rare diseases and may also be cost-effective for treatment guidance under favorable conditions. Methodological rigor tended to be higher in treatment guidance studies, whereas EEs in pediatric diagnostics faced greater challenges. Utility values were largely derived from a common survey using validated multi-attribute utility instruments, and studied on proxy conditions. Variability in perspectives, target populations, and costs limited comparability. To strengthen future EEs, standardized methodologies and long-term, real-world data on clinical and non-clinical benefits are needed. Conclusion: Traditional CUA approaches are essential to guide the implementation of new technologies, but they should be accommodated or complemented by alternative methods, innovative and comprehensive frameworks that capture the broader value of GS/ES and support their integration into clinical and public health practice.

Measuring the health benefits of genome and exome sequencing. A systematic review of economic evaluations / Riccio, Marianna; Rosso, Annalisa; Siena, Leonardo Maria; Baccolini, Valentina; Migliara, Giuseppe; Sciurti, Antonio; Isonne, Claudia; Iera, Jessica; Pierri, Francesco; Marzuillo, Carolina; De Vito, Corrado; La Torre, Giuseppe; Villari, Paolo. - In: FRONTIERS IN PUBLIC HEALTH. - ISSN 2296-2565. - 13:(2025), pp. 1-17. [10.3389/fpubh.2025.1728978]

Measuring the health benefits of genome and exome sequencing. A systematic review of economic evaluations

Riccio, Marianna
Co-primo
;
Rosso, Annalisa
Co-primo
;
Siena, Leonardo Maria;Baccolini, Valentina
;
Migliara, Giuseppe;Sciurti, Antonio;Isonne, Claudia;Iera, Jessica;Pierri, Francesco;Marzuillo, Carolina;De Vito, Corrado;La Torre, Giuseppe;Villari, Paolo
2025

Abstract

Introduction: Genome sequencing (GS) and exome sequencing (ES) technologies have gained increasing attention in health economics for evaluating their clinical and public health introduction, but their complexity challenges traditional methods. This systematic review aimed to investigate and discuss full economic evaluations (EEs) of GS and ES in relation to health outcomes, with a focus on methodological issues. Methods: A systematic search of several databases was carried out (PROSPERO CRD42023430992). Quality was evaluated using the Quality of Health Economic Studies instrument. Key methodological features were investigated, and a narrative synthesis of the findings was performed after grouping studies by testing scope. Results: Overall, 12 recently published cost-utility analyses (CUAs) were included, assessing the use of GS/ES for guiding targeted therapy in oncology (N = 4) or major depressive disorder (N = 1), and diagnosing rare genetic diseases (N = 7). The findings suggested that GS/ES may be cost-effective for diagnosing rare diseases and may also be cost-effective for treatment guidance under favorable conditions. Methodological rigor tended to be higher in treatment guidance studies, whereas EEs in pediatric diagnostics faced greater challenges. Utility values were largely derived from a common survey using validated multi-attribute utility instruments, and studied on proxy conditions. Variability in perspectives, target populations, and costs limited comparability. To strengthen future EEs, standardized methodologies and long-term, real-world data on clinical and non-clinical benefits are needed. Conclusion: Traditional CUA approaches are essential to guide the implementation of new technologies, but they should be accommodated or complemented by alternative methods, innovative and comprehensive frameworks that capture the broader value of GS/ES and support their integration into clinical and public health practice.
2025
cost-effectiveness; cost-utility; economic evaluation; exome sequencing (es); genome sequencing (gs); systematic review
01 Pubblicazione su rivista::01g Articolo di rassegna (Review)
Measuring the health benefits of genome and exome sequencing. A systematic review of economic evaluations / Riccio, Marianna; Rosso, Annalisa; Siena, Leonardo Maria; Baccolini, Valentina; Migliara, Giuseppe; Sciurti, Antonio; Isonne, Claudia; Iera, Jessica; Pierri, Francesco; Marzuillo, Carolina; De Vito, Corrado; La Torre, Giuseppe; Villari, Paolo. - In: FRONTIERS IN PUBLIC HEALTH. - ISSN 2296-2565. - 13:(2025), pp. 1-17. [10.3389/fpubh.2025.1728978]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1762230
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