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
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
605-611Références
Health Technol Assess. 2007 Nov;11(45):iii-iv, ix-221
pubmed: 17999840
BMC Med Res Methodol. 2012 Feb 01;12:9
pubmed: 22297116
J Clin Oncol. 2015 Jul 10;33(20):2296-302
pubmed: 26014296
Neuro Oncol. 2010 Jul;12(7):725-35
pubmed: 20364023
Lancet Oncol. 2009 May;10(5):459-66
pubmed: 19269895
Cancer. 2008 Mar 15;112(6):1337-44
pubmed: 18213621
CNS Oncol. 2018 Jul 1;7(3):CNS23
pubmed: 30124334
JAMA. 2017 Dec 19;318(23):2306-2316
pubmed: 29260225
J Cancer Res Clin Oncol. 2010 Nov;136(11):1691-5
pubmed: 20177703
Neuro Oncol. 2016 Aug;18(8):1129-36
pubmed: 27177573
Neuroepidemiology. 2011;36(4):230-9
pubmed: 21677447
PLoS One. 2012;7(4):e34588
pubmed: 22511951
J Med Econ. 2019 Oct;22(10):1006-1013
pubmed: 31050315
J Neurooncol. 2018 Jun;138(2):359-367
pubmed: 29468446
Neuro Oncol. 2013 Nov;15(11):1532-42
pubmed: 23935155
N Engl J Med. 2014 Feb 20;370(8):699-708
pubmed: 24552317
Ann Oncol. 2014 Sep;25 Suppl 3:iii93-101
pubmed: 24782454
JAMA. 2015 Dec 15;314(23):2535-43
pubmed: 26670971
Med Decis Making. 2017 May;37(4):427-439
pubmed: 27698003
Nat Rev Neurol. 2015 Sep;11(9):504-14
pubmed: 26260659
N Engl J Med. 2005 Mar 10;352(10):987-96
pubmed: 15758009
N Engl J Med. 2014 Feb 20;370(8):709-22
pubmed: 24552318