Maintenance erlotinib in advanced nonsmall cell lung cancer: cost-effectiveness in EGFR wild-type across Europe

被引:17
|
作者
Walleser, Silke [1 ]
Ray, Joshua [2 ]
Bischoff, Helge [3 ]
Vergnenegre, Alain [4 ]
Rosery, Hubertus [5 ]
Chouaid, Christos [6 ]
Heigener, David [7 ]
de Castro Carpeno, Javier [8 ]
Tiseo, Marcello [9 ]
Walzer, Stefan [2 ]
机构
[1] Hlth Econ Consultancy, Renens, Switzerland
[2] F Hoffmann La Roche Pharmaceut AG, Basel, Switzerland
[3] Thorac Hosp Heidelberg, Heidelberg, Germany
[4] Limoges Univ Hosp, Limoges, France
[5] Assessment In Med GmbH, Marie Curie Str 8, D-79539 Lorrach, Germany
[6] Hosp St Antoine, Paris, France
[7] Hosp Grosshansdorf, Grosshansdorf, Germany
[8] Univ Hosp La Paz, Madrid, Spain
[9] Univ Hosp Parma, Parma, Italy
来源
CLINICOECONOMICS AND OUTCOMES RESEARCH | 2012年 / 4卷
关键词
nonsmall cell lung cancer; erlotinib; cost-benefit analysis; epidermal growth factor receptor; wild-type; Europe;
D O I
10.2147/CEOR.S31794
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: First-line maintenance erlotinib in patients with locally advanced or metastatic nonsmall cell lung cancer (NSCLC) has demonstrated significant overall survival and progression-free survival benefits compared with best supportive care plus placebo, irrespective of epidermal growth factor receptor (EGFR) status (SATURN trial). The cost-effectiveness of first-line maintenance erlotinib in the overall SATURN population has been assessed and published recently, but analyses according to EGFR mutation status have not been performed yet, which was the rationale for assessing the cost-effectiveness of first-line maintenance erlotinib specifically in EGFR wild-type metastatic NSCLC. Methods: The incremental cost per life-year gained of first-line maintenance erlotinib compared with best supportive care in patients with EGFR wild-type stable metastatic NSCLC was assessed for five European countries (the United Kingdom, Germany, France, Spain, and Italy) with an area-under-the-curve model consisting of three health states (progression-free survival, progressive disease, death). Log-logistic survival functions were fitted to Phase III patient-level data (SATURN) to model progression-free survival and overall survival. The first-line maintenance erlotinib therapy cost (modeled for time to treatment cessation), medication cost in later lines, and cost for the treatment of adverse events were included. Deterministic and probabilistic sensitivity analyses using Monte Carlo simulation (1000 iterations) were performed. Results: According to the model simulations, first-line maintenance erlotinib compared with best supportive care in EGFR wild-type stable metastatic NSCLC resulted in 4.57 months of life gained (17.82 months for erlotinib versus 13.24 months for best supportive care) and 1.14 months of life without progression gained (erlotinib 4.29 versus best supportive care 3.15), and incremental total costs of erlotinib from (sic)7897 (UK) to (sic)9580 (Germany). The corresponding mean incremental cost per life-year gained of erlotinib ranged between (sic)20,711 (UK) and (sic)25,124 (Germany). Sensitivity analyses confirmed these results. Conclusion: First-line erlotinib maintenance treatment is cost-effective compared with best supportive care in EGFR wild-type stable metastatic NSCLC, irrespective of the country setting.
引用
收藏
页码:269 / 275
页数:7
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