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

e20180255

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Auteurs

Pedro Aguiar (P)

Faculdade de Medicina do ABC, Santo André, SP, Brazil.

Felipe Roitberg (F)

Instituto do Câncer de São Paulo Octavio Frias de Oliveira, São Paulo, SP, Brasil.

Gilberto Lopes (G)

Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL, USA.

Auro Del Giglio (AD)

Centro de Estudos e Pesquisa de Hematologia e Oncologia, Faculdade de Medicina do ABC, Santo André, SP, Brazil.

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Classifications MeSH