Cost-effectiveness of tumor-treating fields added to maintenance temozolomide in patients with glioblastoma: an updated evaluation using a partitioned survival model.


Journal

Journal of neuro-oncology
ISSN: 1573-7373
Titre abrégé: J Neurooncol
Pays: United States
ID NLM: 8309335

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 31 03 2019
accepted: 16 05 2019
revised: 13 05 2019
pubmed: 28 5 2019
medline: 21 12 2019
entrez: 26 5 2019
Statut: ppublish

Résumé

A first cost-effectiveness analysis has raised a strong concern regarding the cost of tumor treatment fields (TTF) added to maintenance temozolomide for patients with glioblastoma. This evaluation was based on effectiveness outcomes from an interim analysis of the pivotal trial, moreover it used a "standard" Markov model. Our objective was to update the cost-effectiveness evaluation using the more flexible potential of the "partitioned survival" model design and using the latest effectiveness data. We developed the model with three mutually exclusive health states: stable disease, progressive disease, and dead. Good fit parametric models were developed for overall survival and progression free survival and these generated clinically plausible extrapolations beyond the observed data. We adopted the perspective of the French national health insurance and used a 20-year time horizon. Results were expressed as cost/life-years (LY) gained (LYG). The base case model generated incremental benefit of 0.604 LY at a cost of €453,848 which, after 4% annual discounting of benefits and costs, yielded an incremental cost effectiveness ratio (ICER) of €510,273/LYG. Using sensitivity analyses and bootstrapping methods results were found to be relatively robust and were only sensitive to TTF device costs and the modelling of overall survival. To achieve an ICER below €100,000/LYG would require a reduction in TTF device cost of approximately 85%. Using a different type of model and updated survival outcomes, our results show TTF remains an intervention that is not cost-effective, which greatly restrains its diffusion to potentially eligible patients.

Identifiants

pubmed: 31127507
doi: 10.1007/s11060-019-03197-w
pii: 10.1007/s11060-019-03197-w
doi:

Substances chimiques

Antineoplastic Agents, Alkylating 0
Temozolomide YF1K15M17Y

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

605-611

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Auteurs

Martin Connock (M)

Warwick Medical School, University of Warwick, Gibbet Hill Road, Coventry, CV47AL, UK.

Peter Auguste (P)

Warwick Medical School, University of Warwick, Gibbet Hill Road, Coventry, CV47AL, UK.

Claude Dussart (C)

University of Lyon, EA 4129 P2S (Parcours, Santé, Systémique), Lyon, France.

Jacques Guyotat (J)

Pierre Wertheimer Hospital, Neurosurgery Department, Lyon, France.

Xavier Armoiry (X)

Warwick Medical School, University of Warwick, Gibbet Hill Road, Coventry, CV47AL, UK. xavier.armoiry@univ-lyon1.fr.
Pharmacy Department, Edouard Herriot Hospital, Lyon, France. xavier.armoiry@univ-lyon1.fr.
Public Health Department, School of Pharmacy (ISPB)/ UMR CNRS MATEIS, Claude Bernard University Lyon 1, University of Lyon, 8 Avenue Rockefeller, 69008, Lyon, France. xavier.armoiry@univ-lyon1.fr.

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Classifications MeSH