Cost-effectiveness model of renal cell carcinoma (RCC) surveillance in hereditary leiomyomatosis and renal cell carcinoma (HLRCC).


Journal

Journal of medical genetics
ISSN: 1468-6244
Titre abrégé: J Med Genet
Pays: England
ID NLM: 2985087R

Informations de publication

Date de publication:
01 2023
Historique:
received: 22 09 2021
accepted: 11 01 2022
pubmed: 6 2 2022
medline: 28 12 2022
entrez: 5 2 2022
Statut: ppublish

Résumé

To determine the cost-effectiveness of annual renal imaging surveillance (RIS) in hereditary leiomyomatosis and renal cell cancer (HLRCC). HLRCC is associated with a 21% risk to age 70 years of RCC. Presentations with advanced renal cell cancer (RCC) are associated with poor outcomes whereas RIS detects early-stage RCC; however, evidence for the cost-effectiveness of RIS is lacking. We developed a decision-analytic model to compare, at different age starting points (11 years, 18 years, 40 years, 60 years), the costs and benefits of lifetime contrast-enhanced renal MRI surveillance (CERMRIS) vs no surveillance in HLRCC. Benefits were measured in life-years gained (LYG), quality-adjusted life years (QALYs) and costs in British Pounds Sterling (GBP). Net monetary benefit (NMB) was calculated using a cost-effectiveness threshold of £20 000/QALY. One-way sensitivity and probabilistic analyses were also performed. In the base-case 11-year age cohort, surveillance was cost-effective (Incremental_NMB=£3522 (95% CI -£2747 to £7652); Incremental_LYG=1.25 (95% CI 0.30 to 1.86); Incremental_QALYs=0.29 (95% CI 0.07 to 0.43)] at an additional mean discounted cost of £2185/patient (95% CI £430 to £4144). Surveillance was also cost-effective in other age cohorts and dominated a no surveillance strategy in the 40 year cohort [Incremental_NMB=£12 655 (95% CIs -£709 to £21 134); Incremental_LYG=1.52 (95% CI 0.30 to 2.26); Incremental_QALYs=0.58 (95% CI 0.12 to 0.87) with a cost saving of £965/patient (95% CI -£4202 to £2652). Annual CERMRI in HLRCC is cost-effective across age groups modelled.

Identifiants

pubmed: 35121648
pii: jmedgenet-2021-108215
doi: 10.1136/jmedgenet-2021-108215
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

41-47

Subventions

Organisme : Department of Health
ID : IS-BRC1215-20007
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C64726/A30910
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: AJT declares conflicts with Perspectum. DGE declares consultancies with AstraZeneca, SpringWorks and Recursion and declares no conflict of interest specifically related to this study. The other authors declare no conflicts of interest.

Auteurs

Alexander J Thompson (AJ)

Manchester Centre for Health Economics, Division of Population Health, Health Services Research and Primary Care, The University of Manchester, Manchester, UK.

Yousef M Alwan (YM)

Department of Clinical Radiology, Manchester University NHS Foundation Trust, Manchester, UK.

Vijay A C Ramani (VAC)

Department of Urology, The Christie NHS Foundation Trust, Manchester, UK.

D Gareth Evans (DG)

Division of Evolution and Genomic Medicine, The University of Manchester, Manchester, UK.
Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Manchester, UK.

Eamonn R Maher (ER)

Department of Medical Genetics, University of Cambridge and Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.

Emma R Woodward (ER)

Division of Evolution and Genomic Medicine, The University of Manchester, Manchester, UK Emma.Woodward@mft.nhs.uk.
Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Manchester, UK.

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