Arrieta Oscar, Anaya Pablo, Morales-Oyarvide Vicente, Ramírez-Tirado Laura Alejandra, Polanco Ana C
Unit of Thoracic Oncology, Instituto Nacional de Cancerología (INCan), San Fernando #22, Col. Sección XVI, Tlalpan, 14080, México City, Mexico.
IMS Health, Mexico City, Mexico.
Eur J Health Econ. 2016 Sep;17(7):855-63. doi: 10.1007/s10198-015-0726-5. Epub 2015 Sep 4.
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.
评估在墨西哥医疗机构中,吉非替尼或卡铂-紫杉醇一线治疗晚期非小细胞肺癌(NSCLC)时,表皮生长因子受体(EGFR)突变检测策略的成本效益。
采用离散事件模拟(DES)模型进行成本效益分析,以模拟晚期NSCLC患者的两种治疗策略。策略一包括对患者进行EGFR突变检测并据此给予治疗。策略二包括对所有患者不进行检测直接化疗。所有结果均以2014年美元表示。分析采用墨西哥EGFR突变发生率的数据。对EGFR患病率进行单因素敏感性分析。无进展生存期(PFS)转移概率根据易瑞沙(IPASS)研究的数据进行估计,并用威布尔分布进行模拟,通过平行试验运行以计算概率敏感性分析。
检测策略组患者的PFS为6.76个月(%95CI6.10 - 7.44),而未检测组为5.85个月(%95CI5.43 - 6.29)。单向敏感性分析表明,PFS与EGFR突变患病率呈直接关系,而增量成本效果比(ICER)和检测成本与EGFR突变患病率呈反比关系。概率敏感性分析表明,与策略二相比,策略一的所有迭代均具有增量成本和增量PFS。
ICER与EGFR检测成本之间存在直接关系,与EGFR突变患病率呈反比关系。当患病率>10%时,ICER保持不变。本研究可能会影响墨西哥和拉丁美洲关于晚期NSCLC突变检测和治疗的卫生政策。