Princess Margaret Cancer Centre/University Health Network, Toronto, Ontario, Canada.
University of Toronto, Toronto, Ontario, Canada.
Lung Cancer. 2018 Nov;125:1-7. doi: 10.1016/j.lungcan.2018.08.024. Epub 2018 Aug 30.
Osimertinib improves progression-free survival in previously untreated EGFR-positive advanced non-small cell lung cancer (NSCLC) patients, with marked intracranial response rates. However, its cost-effectiveness in a publically funded health care system has not been established. We assessed the cost-effectiveness of first-line osimertinib from the public payer perspective in the Canadian health care system.
A Markov model was developed to project the outcomes and direct medical costs of initial treatment with osimertinib or current standard-of-care (SoC) EGFR TKIs, gefinitib or afatinib, in patients with previously untreated EGFR-mutant advanced NSCLC. Clinical and cost input estimates were informed from the available literature. Model outcomes included costs (in 2018 Canadian dollars), life years (LYs), quality-adjusted life-years (QALYs), and the cost utility of osimertinib compared to SoC EGFR TKI, or incremental cost per QALY gained.
Initial treatment with osimertinib was associated with a gain of 0.79 QALY [95% confidence interval (CI), 0.74 to 0.83] at an incremental cost of $176,394 CAD (95% CI, 176,383 to 176,405) vs. SoC EGFR TKI (incremental cost-effectiveness ratio [ICER]: $223,133/QALY gained; 95%CI, 198,144 to 252,805). Osimertinib had a 0% probability of being cost-effective at a willingness-to-pay threshold of $100,000 per QALY. Deterministic sensitivity analysis showed that the cost of osimertinib had the largest impact on ICER results.
At the current marketed price, first-line osimertinib therapy in patients with advanced EGFR-mutant lung adenocarcinoma is not cost-effective in Canada. Reduction of osimertinib cost, for example by 25%, can significantly improve the cost-effectiveness profile.
奥希替尼可改善未经治疗的 EGFR 阳性晚期非小细胞肺癌(NSCLC)患者的无进展生存期,且颅内缓解率显著。然而,其在公共资助的医疗保健系统中的成本效益尚未确定。我们从加拿大公共医保的角度评估了奥希替尼在加拿大医保系统中的成本效益。
采用马尔可夫模型,预测初治 EGFR 突变晚期 NSCLC 患者初始接受奥希替尼或当前标准治疗(SoC)EGFR-TKI(吉非替尼或阿法替尼)的治疗结果和直接医疗成本。临床和成本投入估算来自现有文献。模型结果包括成本(2018 加元)、寿命年(LY)、质量调整寿命年(QALY)和奥希替尼与 SoC EGFR-TKI 的成本效用,或增量成本每获得一个 QALY。
初始接受奥希替尼治疗可获得 0.79 个 QALY 的获益[95%置信区间(CI):0.74 至 0.83],增量成本为 176,394 加元(95%CI:176,383 至 176,405),而接受 SoC EGFR-TKI 治疗的增量成本-效果比(ICER)为 223,133 加元/QALY 获益(95%CI:198,144 至 252,805)。奥希替尼的增量成本-效果比在 100,000 加元/QALY 的意愿支付阈值下,其获益概率为 0%。确定性敏感性分析表明,奥希替尼的成本对 ICER 结果的影响最大。
按照目前的上市价格,加拿大初治的晚期 EGFR 突变肺腺癌患者使用奥希替尼治疗的成本效益不高。奥希替尼的成本降低 25%,可以显著改善其成本效益状况。