Liu Wenjie, Huo Gengwei, Chen Peng
Department of Thoracic Oncology, Tianjin Medical University Cancer Institute and Hospital, Key Laboratory of Cancer Prevention and Therapy of Tianjin, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Tianjin, China.
Front Pharmacol. 2023 Jul 20;14:1163381. doi: 10.3389/fphar.2023.1163381. eCollection 2023.
In the open-label phase III POSEIDON randomized clinical trial (RCT), a limited course of tremelimumab plus durvalumab and chemotherapy (T + D + CT) indicated in the first-line treatment of metastatic non-small cell lung cancer (mNSCLC), progression-free survival, and overall survival (OS) were substantially improved without significant additional tolerance burden compared to chemotherapy (CT). However, given the high cost of T + D + CT, its value needs to be evaluated in terms of both potency and cost. To evaluate the cost-effectiveness of T + D + CT CT in individuals with previously untreated mNSCLC from a U.S. payer perspective. A three-state Markov model was adopted to weigh the lifetime costs and effectiveness of T + D + CT CT for the treatment of first-line mNSCLC, according to the results of the POSEIDON phase III RCT involving 675 individuals with mNSCLC. Individuals were simulated to undergo either T + D + CT for up to four 21-day cycles, followed by durvalumab once every 4 weeks until disease progression or unacceptable toxic effects and one additional tremelimumab dose, or CT for up to six 21-day cycles (with or without pemetrexed maintenance; all groups) in the analysis. Lifetime costs, quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratio (ICER) were evaluated with a willingness-to-pay (WTP) threshold of $ 100,000 to $ 150,000 per QALY. The uncertainty of the model was investigated using univariate and probabilistic sensitivity analysis. T + D + CT produced additional 0.36 QALYs with additional costs of $ 217,694, compared to CT, giving rise to ICERs of $ 608,667.86/QALY. The univariate sensitivity analysis demonstrated that the outcomes were most sensitive to the cost of durvalumab. Other variables with a large or moderate influence were the utility of progression-free survival state, utility of progressive disease state, and cost of tremelimumab. Probability sensitivity analysis revealed that T + D + CT had a 0% probability of cost-effectiveness in individuals with mNSCLC at a willingness-to-pay threshold of $ 100,000 to $ 150,000 per QALY. In this model, T + D + CT was estimated to be less cost-effective than CT for patients with mNSCLC at a WTP threshold of $ 100,000 to $ 150,000 per QALY in the United States. When new combination therapies with remarkable effect become pivotal in the first-line treatment, the price reduction of durvalumab and tremelimumab may be necessary to achieve cost-effectiveness in future possible context.
在开放标签的III期POSEIDON随机临床试验(RCT)中,用于转移性非小细胞肺癌(mNSCLC)一线治疗的有限疗程的曲美木单抗联合度伐利尤单抗及化疗(T+D+CT)与化疗(CT)相比,无进展生存期和总生存期(OS)显著改善,且无明显额外的耐受性负担。然而,鉴于T+D+CT成本高昂,其价值需要在疗效和成本两方面进行评估。从美国医保支付方的角度评估T+D+CT用于既往未治疗的mNSCLC患者的成本效益。根据POSEIDON III期RCT涉及675例mNSCLC患者的结果,采用三状态马尔可夫模型权衡T+D+CT治疗一线mNSCLC的终身成本和疗效。在分析中,模拟患者接受长达四个21天周期的T+D+CT治疗,随后每4周接受一次度伐利尤单抗治疗,直至疾病进展或出现不可接受的毒性反应,以及额外一剂曲美木单抗,或接受长达六个21天周期的CT治疗(有或无培美曲塞维持治疗;所有组)。以每质量调整生命年(QALY)100,000美元至150,000美元的支付意愿(WTP)阈值评估终身成本、QALY和增量成本效益比(ICER)。使用单变量和概率敏感性分析研究模型的不确定性。与CT相比,T+D+CT额外产生0.36个QALY,额外成本为217,694美元,导致ICER为608,667.86美元/QALY。单变量敏感性分析表明,结果对度伐利尤单抗的成本最为敏感。其他具有较大或中等影响的变量是无进展生存状态的效用、疾病进展状态的效用以及曲美木单抗的成本。概率敏感性分析显示,在每QALY支付意愿阈值为100,000美元至150,000美元的情况下,T+D+CT在mNSCLC患者中具有成本效益的概率为0%。在该模型中,在美国每QALY支付意愿阈值为100,000美元至150,000美元时,估计T+D+CT对mNSCLC患者的成本效益低于CT。当具有显著疗效的新联合疗法在一线治疗中成为关键时,可能需要降低度伐利尤单抗和曲美木单抗的价格,以便在未来可能的情况下实现成本效益。