Cost-effectiveness analysis of EGFR mutation testing in patients with non-small cell lung cancer (NSCLC) with gefitinib or carboplatin-paclitaxel
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作者:
Arrieta, Oscar
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INCan, Unit Thorac Oncol, San Fernando 22,Col Secc 16, Mexico City 14080, DF, MexicoINCan, Unit Thorac Oncol, San Fernando 22,Col Secc 16, Mexico City 14080, DF, Mexico
Arrieta, Oscar
[1
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Anaya, Pablo
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IMS Hlth, Mexico City, DF, MexicoINCan, Unit Thorac Oncol, San Fernando 22,Col Secc 16, Mexico City 14080, DF, Mexico
Anaya, Pablo
[2
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Morales-Oyarvide, Vicente
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INCan, Unit Thorac Oncol, San Fernando 22,Col Secc 16, Mexico City 14080, DF, MexicoINCan, Unit Thorac Oncol, San Fernando 22,Col Secc 16, Mexico City 14080, DF, Mexico
Morales-Oyarvide, Vicente
[1
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Alejandra Ramirez-Tirado, Laura
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INCan, Unit Thorac Oncol, San Fernando 22,Col Secc 16, Mexico City 14080, DF, MexicoINCan, Unit Thorac Oncol, San Fernando 22,Col Secc 16, Mexico City 14080, DF, Mexico
Alejandra Ramirez-Tirado, Laura
[1
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Polanco, Ana C.
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AstraZeneca, Mexico City, DF, MexicoINCan, Unit Thorac Oncol, San Fernando 22,Col Secc 16, Mexico City 14080, DF, Mexico
Polanco, Ana C.
[3
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机构:
[1] INCan, Unit Thorac Oncol, San Fernando 22,Col Secc 16, Mexico City 14080, DF, Mexico
Assess the cost-effectiveness of an EGFR-mutation testing strategy for advanced NSCLC in first-line therapy with either gefitinib or carboplatin-paclitaxel in Mexican institutions. Cost-effectiveness analysis using a discrete event simulation (DES) model to simulate two therapeutic strategies in patients with advanced NSCLC. Strategy one included patients tested for EGFR-mutation and therapy given accordingly. Strategy two included chemotherapy for all patients without testing. All results are presented in 2014 US dollars. The analysis was made with data from the Mexican frequency of EGFR-mutation. A univariate sensitivity analysis was conducted on EGFR prevalence. Progression-free survival (PFS) transition probabilities were estimated on data from the IPASS and simulated with a Weibull distribution, run with parallel trials to calculate a probabilistic sensitivity analysis. PFS of patients in the testing strategy was 6.76 months (95 % CI 6.10-7.44) vs 5.85 months (95 % CI 5.43-6.29) in the non-testing group. The one-way sensitivity analysis showed that PFS has a direct relationship with EGFR-mutation prevalence, while the ICER and testing cost have an inverse relationship with EGFR-mutation prevalence. The probabilistic sensitivity analysis showed that all iterations had incremental costs and incremental PFS for strategy 1 in comparison with strategy 2. There is a direct relationship between the ICER and the cost of EGFR testing, with an inverse relationship with the prevalence of EGFR-mutation. When prevalence is > 10 % ICER remains constant. This study could impact Mexican and Latin American health policies regarding mutation detection testing and treatment for advanced NSCLC.
机构:
Keio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, JapanKeio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, Japan
Narita, Yusuke
Matsushima, Yukiko
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Keio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, JapanKeio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, Japan
Matsushima, Yukiko
Shiroiwa, Takeru
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Natl Inst Publ Hlth, Dept Hlth & Welf Serv, Saitama, JapanKeio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, Japan
Shiroiwa, Takeru
Chiba, Koji
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Yokohama Univ Pharm, Lab Clin Pharmacol, Yokohama, Kanagawa, JapanKeio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, Japan
Chiba, Koji
Nakanishi, Yoichi
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Kyushu Univ, Fac Med Sci, Dept Clin Med, Chest Dis Res Inst, Fukuoka 812, JapanKeio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, Japan
Nakanishi, Yoichi
Kurokawa, Tatsuo
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Keio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, JapanKeio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, Japan
Kurokawa, Tatsuo
Urushihara, Hisashi
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Keio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, JapanKeio Univ, Fac Pharm, Dept Drug Dev & Regulatory Sci, Tokyo 1058512, Japan