Cost-effectiveness of Osimertinib in the First-Line Treatment of Patients With EGFR-Mutated Advanced Non-Small Cell Lung Cancer

被引:100
|
作者
Aguiar, Pedro N., Jr. [1 ]
Haaland, Benjamin [2 ,3 ]
Park, Wungki [4 ]
Tan, Pui San [5 ]
del Giglio, Auro [1 ]
Lopes, Gilberto de Lima, Jr. [4 ]
机构
[1] Fac Med ABC, Estudos & Pesquisa Hematol & Oncol, Santo Andre, Brazil
[2] Univ Utah, Dept Populat Hlth Sci, Huntsman Canc Inst, Salt Lake City, UT USA
[3] Univ Utah, Dept Internal Med, Salt Lake City, UT 84112 USA
[4] Univ Miami, Sylvester Comprehens Canc Ctr, 1120 NW14th St,Ste 650J, Miami, FL 33135 USA
[5] Univ Oxford, Nuffield Dept Primary Care Hlth Sci, Oxford, England
关键词
BREAST-CANCER; OPEN-LABEL; CHEMOTHERAPY; DRUGS;
D O I
10.1001/jamaoncol.2018.1395
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
IMPORTANCE The survival of patients with advanced non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) gene mutations has improved substantially in the last decade with the development of targeted tyrosine kinase inhibitors (TKIs). Osimertinib, a third-generation TKI that is approved by the US Food and Drug Administration for the treatment of patients who develop EGFR T790M mutations, has recently shown improved clinical outcomes compared with gefitinib and erlotinib for treatment-naive patients. OBJECTIVE The aim of this study was to assess the cost-effectiveness of osimertinib for the first-line treatment of patients with EGFR-mutated NSCLC. DESIGN, SETTING, AND PARTICIPANTS For this cost-effectiveness analysis, we extracted individual patient data from the FLAURA randomized clinical trial and used findings of our earlier meta-analysis to develop a decision-analytic model and determine the cost-effectiveness of osimertinib (AZD9291) compared with first-and second-generation EGFR-TKIs over a 10-year time horizon. All direct costs were based on US and Brazilian payer perspectives. MAIN OUTCOMES AND MEASURES The main outcome of this study was the incremental cost-effectiveness ratio (ICER) expressed as cost per quality-adjusted life-year (QALY) gained by using osimertinib compared with first-or second-generation EGFR-TKIs in previously untreated EGFR-mutated NSCLC. RESULTS In the base case using the data as reported in the FLAURA trial, the incremental QALY for osimertinib was 0.594 compared with the first-and second-generation EGFR-TKIs. In the United States, the osimertinib ICERs were $226 527 vs erlotinib, $231 123 vs gefitinib, and $219 874 vs afatinib. In Brazil, the ICERs were $162 329, $180 804, and $175 432, respectively. The overall survival (95% CI) reported in the FLAURA trial (hazard ratio, 0.63; 95% CI, 0.45-0.88) had the strongest association with the ICER (ranging from $84 342 to $859 771). Osimertinib price adjustments to the FLAURA trial data improved cost-effectiveness. For example, a discount of 10% on osimertinib acquisition cost was associated with a 20% decreased ICER compared with the base case ICER, and a discount of 20% on osimertinib acquisition cost was associated with a 40% decreased ICER compared with the base case ICER. CONCLUSIONS AND RELEVANCE At current costs, by World Health Organization cost-effectiveness threshold criteria, osimertinib is not cost-effective for first-line therapy of EGFR-mutated NSCLC in either the United States or Brazil.
引用
收藏
页码:1080 / 1084
页数:5
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