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Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care

Genomic research is driving discovery for future population benefit. Limited evidence exists on immediate patient and health system impacts of research participation. This study uses real-world data and quasi-experimental matching to examine early-stage cost and health impacts of research-based geno...

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Autores principales: Weymann, Deirdre, Laskin, Janessa, Jones, Steven J. M., Roscoe, Robyn, Lim, Howard J., Renouf, Daniel J., Schrader, Kasmintan A., Sun, Sophie, Yip, Stephen, Marra, Marco A., Regier, Dean A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628132/
https://www.ncbi.nlm.nih.gov/pubmed/34843087
http://dx.doi.org/10.1007/s12687-021-00557-w
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author Weymann, Deirdre
Laskin, Janessa
Jones, Steven J. M.
Roscoe, Robyn
Lim, Howard J.
Renouf, Daniel J.
Schrader, Kasmintan A.
Sun, Sophie
Yip, Stephen
Marra, Marco A.
Regier, Dean A.
author_facet Weymann, Deirdre
Laskin, Janessa
Jones, Steven J. M.
Roscoe, Robyn
Lim, Howard J.
Renouf, Daniel J.
Schrader, Kasmintan A.
Sun, Sophie
Yip, Stephen
Marra, Marco A.
Regier, Dean A.
author_sort Weymann, Deirdre
collection PubMed
description Genomic research is driving discovery for future population benefit. Limited evidence exists on immediate patient and health system impacts of research participation. This study uses real-world data and quasi-experimental matching to examine early-stage cost and health impacts of research-based genomic sequencing. British Columbia’s Personalized OncoGenomics (POG) single-arm program applies whole genome and transcriptome analysis (WGTA) to characterize genomic landscapes in advanced cancers. Our cohort includes POG patients enrolled between 2014 and 2015 and 1:1 genetic algorithm–matched usual care controls. We undertake a cost consequence analysis and estimate 1-year effects of WGTA on patient management, patient survival, and health system costs reported in 2015 Canadian dollars. WGTA costs are imputed and forecast using system of equations modeling. We use Kaplan-Meier survival analysis to explore survival differences and inverse probability of censoring weighted linear regression to estimate mean 1-year survival times and costs. Non-parametric bootstrapping simulates sampling distributions and enables scenario analysis, revealing drivers of incremental costs, survival, and net monetary benefit for assumed willingness to pay thresholds. We identified 230 POG patients and 230 matched controls for cohort inclusion. The mean period cost of research-funded WGTA was $26,211 (SD: $14,191). Sequencing costs declined rapidly, with WGTA forecasts hitting $13,741 in 2021. The incremental healthcare system effect (non-research expenditures) was $5203 (95% CI: 75, 10,424) compared to usual care. No overall survival differences were observed, but outcome heterogeneity was present. POG patients receiving WGTA-informed treatment experienced incremental survival gains of 2.49 months (95% CI: 1.32, 3.64). Future cost consequences became favorable as WGTA cost drivers declined and WGTA-informed treatment rates improved to 60%. Our study demonstrates the ability of real-world data to support evaluations of only-in-research health technologies. We identify situations where precision oncology research initiatives may produce survival benefit at a cost that is within healthcare systems’ willingness to pay. This economic evidence informs the early-stage healthcare impacts of precision oncology research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12687-021-00557-w.
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spelling pubmed-86281322021-11-29 Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care Weymann, Deirdre Laskin, Janessa Jones, Steven J. M. Roscoe, Robyn Lim, Howard J. Renouf, Daniel J. Schrader, Kasmintan A. Sun, Sophie Yip, Stephen Marra, Marco A. Regier, Dean A. J Community Genet Original Article Genomic research is driving discovery for future population benefit. Limited evidence exists on immediate patient and health system impacts of research participation. This study uses real-world data and quasi-experimental matching to examine early-stage cost and health impacts of research-based genomic sequencing. British Columbia’s Personalized OncoGenomics (POG) single-arm program applies whole genome and transcriptome analysis (WGTA) to characterize genomic landscapes in advanced cancers. Our cohort includes POG patients enrolled between 2014 and 2015 and 1:1 genetic algorithm–matched usual care controls. We undertake a cost consequence analysis and estimate 1-year effects of WGTA on patient management, patient survival, and health system costs reported in 2015 Canadian dollars. WGTA costs are imputed and forecast using system of equations modeling. We use Kaplan-Meier survival analysis to explore survival differences and inverse probability of censoring weighted linear regression to estimate mean 1-year survival times and costs. Non-parametric bootstrapping simulates sampling distributions and enables scenario analysis, revealing drivers of incremental costs, survival, and net monetary benefit for assumed willingness to pay thresholds. We identified 230 POG patients and 230 matched controls for cohort inclusion. The mean period cost of research-funded WGTA was $26,211 (SD: $14,191). Sequencing costs declined rapidly, with WGTA forecasts hitting $13,741 in 2021. The incremental healthcare system effect (non-research expenditures) was $5203 (95% CI: 75, 10,424) compared to usual care. No overall survival differences were observed, but outcome heterogeneity was present. POG patients receiving WGTA-informed treatment experienced incremental survival gains of 2.49 months (95% CI: 1.32, 3.64). Future cost consequences became favorable as WGTA cost drivers declined and WGTA-informed treatment rates improved to 60%. Our study demonstrates the ability of real-world data to support evaluations of only-in-research health technologies. We identify situations where precision oncology research initiatives may produce survival benefit at a cost that is within healthcare systems’ willingness to pay. This economic evidence informs the early-stage healthcare impacts of precision oncology research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12687-021-00557-w. Springer Berlin Heidelberg 2021-11-29 2022-10 /pmc/articles/PMC8628132/ /pubmed/34843087 http://dx.doi.org/10.1007/s12687-021-00557-w Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021
spellingShingle Original Article
Weymann, Deirdre
Laskin, Janessa
Jones, Steven J. M.
Roscoe, Robyn
Lim, Howard J.
Renouf, Daniel J.
Schrader, Kasmintan A.
Sun, Sophie
Yip, Stephen
Marra, Marco A.
Regier, Dean A.
Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care
title Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care
title_full Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care
title_fullStr Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care
title_full_unstemmed Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care
title_short Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care
title_sort early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628132/
https://www.ncbi.nlm.nih.gov/pubmed/34843087
http://dx.doi.org/10.1007/s12687-021-00557-w
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