Distinct models to assess the cost-effectiveness of EGFR-tyrosine kinase inhibitors for the treatment of metastatic non-small cell lung cancer in the context of the Brazilian Unified Health Care System.
Journal
Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia
ISSN: 1806-3756
Titre abrégé: J Bras Pneumol
Pays: Brazil
ID NLM: 101222274
Informations de publication
Date de publication:
Historique:
received:
06
09
2017
accepted:
06
11
2019
entrez:
4
6
2020
pubmed:
4
6
2020
medline:
9
1
2021
Statut:
ppublish
Résumé
Lung cancer is an important health problem due to its high incidence and mortality. The treatment of metastatic disease improved after the molecular pathways of cancer came to be known. However, targeted therapy is unavailable to many patients treated within the Brazilian Sistema Único de Saúde (SUS, Unified Health Care System). Our objective was to assess the cost-effectiveness of erlotinib, gefitinib, and afatinib versus that of chemotherapy for the treatment of non-small cell lung cancer in the context of the SUS. Different analytical models were developed based on data in the literature. The outcomes were presented in quality-adjusted life-years (QALYs) and incremental cost-effectiveness ratios (ICERs) per QALY gained. All costs related to treatment and supportive therapies were included in the models. In one model, data from retrospective studies showed 2.01 life-years saved and a mean QALY gain of 1.169. The ICER per QALY gained ranged from R$48,451.29 (for gefitinib) to R$85,559.22 (for erlotinib). In another model, data from a meta-analysis showed -0.01 life-years saved and a mean QALY gain of 0.178. The ICER per QALY gained ranged from R$27,028.30 (for gefitinib) to R$75,203.26 (for erlotinib). There is no ideal analytical model for the SUS. However, targeted therapy with EGFR-tyrosine kinase inhibitors has been shown to be cost-effective in various scenarios. The adoption of drug price discounts will improve the cost-effectiveness of treatment.
Identifiants
pubmed: 32490907
pii: S1806-37132020000400206
doi: 10.36416/1806-3756/e20180255
pmc: PMC7567624
pii:
doi:
Substances chimiques
Protein Kinase Inhibitors
0
EGFR protein, human
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
Types de publication
Journal Article
Langues
por
eng
Sous-ensembles de citation
IM
Pagination
e20180255Références
N Engl J Med. 2009 Sep 3;361(10):947-57
pubmed: 19692680
J Clin Oncol. 1998 Jul;16(7):2459-65
pubmed: 9667264
J Clin Oncol. 2015 Aug 10;33(23):2563-77
pubmed: 26101248
Int J Cancer. 2015 Mar 1;136(5):E359-86
pubmed: 25220842
Lancet Oncol. 2016 May;17(5):577-89
pubmed: 27083334
Lung Cancer. 2008 Dec;62(3):374-80
pubmed: 18467000
J Clin Oncol. 2000 Jan;18(1):122-30
pubmed: 10623702
J Clin Oncol. 2013 Sep 20;31(27):3327-34
pubmed: 23816960
J Thorac Oncol. 2016 Apr;11(4):556-65
pubmed: 26724471
CA Cancer J Clin. 2016 Jan-Feb;66(1):7-30
pubmed: 26742998
J Natl Cancer Inst. 2017 Jun 1;109(6):
pubmed: 28376144
Exp Ther Med. 2012 Dec;4(6):1035-1038
pubmed: 23226770
Lancet Oncol. 2012 Mar;13(3):239-46
pubmed: 22285168
Health Qual Life Outcomes. 2008 Oct 21;6:84
pubmed: 18939982
Ann Oncol. 1998 May;9(5):475-82
pubmed: 9653486
JAMA Oncol. 2016 Jan;2(1):19-21
pubmed: 26501848