Cost-effectiveness analysis of pembrolizumab versus chemotherapy as first-line treatment in locally advanced or metastatic non-small cell lung cancer with PD-L1 tumor proportion score 1% or greater

被引:53
作者
She, Longjiang [1 ]
Hu, Huabin [2 ]
Liao, Mengting [3 ]
Xia, Xuefeng [4 ]
Shi, Yin [5 ]
Yao, Linli [1 ]
Ding, Dong [1 ]
Zhu, Youwen [1 ]
Zeng, Shan [1 ]
Shen, Liangfang [1 ]
Huang, Jin [1 ]
Carbone, David P. [6 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Oncol, Changsha 410008, Hunan, Peoples R China
[2] Sun Yat Sen Univ, Dept Med Oncol, Affiliated Hosp 6, Guangzhou 510655, Guangdong, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Changsha 410008, Hunan, Peoples R China
[4] GenePlus Beijing Inst, 9th Floor,6 Bldg,Peking Univ Med Ind Pk, Beijing 102206, Peoples R China
[5] Cent South Univ, Dept Pharm, Xiangya Hosp, Changsha 410008, Hunan, Peoples R China
[6] Ohio State Univ, James Thorac Ctr, James Canc Ctr, Barbara J Bonner Chair Lung Canc Res,Med Ctr, Columbus, OH 43210 USA
基金
湖南省自然科学基金;
关键词
Cost-Effectiveness; Pembrolizumab; Non-Small cell lung cancer; OF-CARE CHEMOTHERAPY; STAGE IV; NSCLC; POLYMORPHISMS; NIVOLUMAB; SUSCEPTIBILITY; ASSOCIATION; THERAPY;
D O I
10.1016/j.lungcan.2019.10.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The purpose of this study was to estimate the cost-effectiveness analysis of pembrolizumab versus chemotherapy as first-line treatment in locally advance or metastatic non-small cell lung cancer (NSCLC) with programmed death ligand 1 (PD-L1) tumor proportion score (TPS) 1% or greater from the United States (US) payer perspective. Materials and Methods: This Markov structure was developed to estimate cost and effectiveness of pembrolizumab vs chemotherapy in the first-line treatment of locally advance or metastatic NSCLC based on the data from KEYNOTE-042. Cost and health outcomes were estimated at a willingness-to-pay (WTP) threshold of $150,000 per quality adjusted life year (QALY) in three PD-Ll TPS populations (>= 50%, >= 20% and >= 1%). One-way, two-way and probabilistic sensitivity analysis were to test the model stability. Subgroup analysis were performed in three PD-Ll TPS populations (>= 50%, >= 20% and >= 1%). Results: The incremental costs and QALYs that pembrolizumab yielded, compared with chemotherapy, were $86164.87 and 0.63, $74562.25 and 0.46 and $70886.65 and 0.39 for the populations with a PD-L1 TPS >= 50%, TPS >= 20% and TPS >= 1%, leading an incremental cost-effective ratio (ICER) of $136,228.82, $160,625.98 and $179,530.17 per QALY, respectively. Conclusion: First-line treatment with pembrolizumab is a cost-effective strategy compared with platinum-based chemotherapy when the value of WTP was $150,000 per QALY in locally advanced or metastatic NSCLC patients with PD-Ll TPS >= 50% and without epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) mutations, but not in the TPS >= 20% and 1% populations.
引用
收藏
页码:88 / 94
页数:7
相关论文
共 39 条
[1]  
[Anonymous], CLIN LUNG CANC
[2]  
[Anonymous], 2019, ASP DRUG PRICING FIL
[3]  
[Anonymous], 2018, SEER CANC STAT REV 1
[4]  
[Anonymous], JAMA ONCOL
[5]  
[Anonymous], ANN ONCOL
[6]   Durvalumab after Chemoradiotherapy in Stage III Non-Small-Cell Lung Cancer [J].
Antonia, S. J. ;
Villegas, A. ;
Daniel, D. ;
Vicente, D. ;
Murakami, S. ;
Hui, R. ;
Yokoi, T. ;
Chiappori, A. ;
Lee, K. H. ;
de Wit, M. ;
Cho, B. C. ;
Bourhaba, M. ;
Quantin, X. ;
Tokito, T. ;
Mekhail, T. ;
Planchard, D. ;
Kim, Y. -C. ;
Karapetis, C. S. ;
Hiret, S. ;
Ostoros, G. ;
Kubota, K. ;
Gray, J. E. ;
Paz-Ares, L. ;
de Castro Carpeno, J. ;
Wadsworth, C. ;
Melillo, G. ;
Jiang, H. ;
Huang, Y. ;
Dennis, P. A. ;
Ozguroglu, M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 377 (20) :1919-1929
[7]   Health-related quality-of-life results for pembrolizumab versus chemotherapy in advanced, PD-L1-positive NSCLC (KEYNOTE-024): a multicentre, international, randomised, open-label phase 3 trial [J].
Brahmer, Julie R. ;
Rodriguez-Abreu, Delvys ;
Robinson, Andrew G. ;
Hui, Rina ;
Csoszi, Tibor ;
Fulop, Andrea ;
Gottfried, Maya ;
Peled, Nir ;
Tafreshi, Ali ;
Cuffe, Sinead ;
O'Brien, Mary ;
Rao, Suman ;
Hotta, Katsuyuki ;
Zhang, Jin ;
Lubiniecki, Gregory M. ;
Deitz, Anne C. ;
Rangwala, Reshma ;
Reck, Martin .
LANCET ONCOLOGY, 2017, 18 (12) :1600-1609
[8]   First-Line Nivolumab in Stage IV or Recurrent Non-Small-Cell Lung Cancer [J].
Carbone, D. P. ;
Reck, M. ;
Paz-Ares, L. ;
Creelan, B. ;
Horn, L. ;
Steins, M. ;
Felip, E. ;
van den Heuvel, M. M. ;
Ciuleanu, T. -E. ;
Badin, F. ;
Ready, N. ;
Hiltermann, T. J. N. ;
Nair, S. ;
Juergens, R. ;
Peters, S. ;
Minenza, E. ;
Wrangle, J. M. ;
Rodriguez-Abreu, D. ;
Borghaei, H. ;
Blumenschein, G. R. ;
Villaruz, L. C. ;
Havel, L. ;
Krejci, J. ;
Corral Jaime, J. ;
Chang, H. ;
Geese, W. J. ;
Bhagavatheeswaran, P. ;
Chen, A. C. ;
Socinski, M. A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 376 (25) :2415-2426
[9]   The cost-effectiveness of alectinib in anaplastic lymphoma kinase-positive (ALK plus ) advanced NSCLC previously treated with crizotinib [J].
Carlson, J. J. ;
Canestaro, W. ;
Ravelo, A. ;
Wong, W. .
JOURNAL OF MEDICAL ECONOMICS, 2017, 20 (07) :671-677
[10]   Association of Wnt-Inducible Signaling Pathway Protein 1 Genetic Polymorphisms With Lung Cancer Susceptibility and Platinum-Based Chemotherapy Response [J].
Chen, Juan ;
Yin, Ji-Ye ;
Li, Xiang-Ping ;
Wang, Ying ;
Zheng, Yi ;
Qian, Chen-Yue ;
He, Hui ;
Fang, Chao ;
Wang, Zhan ;
Zhang, Yu ;
Xiao, Ling ;
Wang, Sai-Ying ;
Zhang, Wei ;
Zhou, Hong-Hao ;
Liu, Zhao-Qian .
CLINICAL LUNG CANCER, 2015, 16 (04) :298-+