Department of Pharmacy Administration and Clinical Pharmacy, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China.
International Research Center for Medicinal Administration, Peking University, No.38 Xueyuan Road, Haidian District, Beijing, 100191, China.
Int J Clin Pharm. 2024 Dec;46(6):1427-1435. doi: 10.1007/s11096-024-01800-3. Epub 2024 Oct 1.
Although selpercatinib has shown clinical benefits for rearranged during transfection (RET) fusion-positive non-small cell lung cancer (NSCLC), its cost-effectiveness requires further evaluation.
This study aimed to evaluate the cost-effectiveness of selpercatinib versus chemotherapy and pembrolizumab in the first-line treatment of RET fusion-positive NSCLC from the perspective of the United States (US) payer.
A partitioned survival model was developed based on data from the LIBRETTO-431 trial. Cost and utility values for the health state were obtained from database data or published literature. The measured outcomes included quality-adjusted life-years (QALYs) and the incremental cost-effectiveness ratio (ICER). One-way sensitivity analysis and probabilistic sensitivity analyses (PSA) were conducted to assess the uncertainty of the model.
Selpercatinib increased QALYs in patients with RET fusion-positive NSCLC by 0.90 compared to chemotherapy plus pembrolizumab, with an additional cost of $542,517.45, resulting in an ICER of $603,286.49/QALY, which exceeded the willingness-to-pay (WTP) threshold ($150,000) in the US. One-way sensitivity analysis suggested that the utility of progressed disease, the utility of progression-free survival, the price of selpercatinib, the discount, the price of pemetrexed, and the price of pembrolizumab had the greatest influence on the cost- effectiveness analysis process. In the PSA, 99.9% of the scatter points were distributed above the US WTP threshold of $150,000.
From the perspective of the US payer, selpercatinib is not cost-effective compared to chemotherapy and pembrolizumab for first-line treatment in patients with RET fusion-positive NSCLC.
尽管塞普替尼(Selpercatinib)对转染重排(RET)融合阳性非小细胞肺癌(NSCLC)显示出临床获益,但仍需要进一步评估其成本效益。
本研究旨在从美国(US)支付者的角度评估塞普替尼与化疗和帕博利珠单抗一线治疗 RET 融合阳性 NSCLC 的成本效益。
根据 LIBRETTO-431 试验的数据,建立了一个分割生存模型。从数据库数据或已发表的文献中获取健康状态的成本和效用值。测量的结果包括质量调整生命年(QALYs)和增量成本效益比(ICER)。进行了单因素敏感性分析和概率敏感性分析(PSA),以评估模型的不确定性。
与化疗加帕博利珠单抗相比,塞普替尼使 RET 融合阳性 NSCLC 患者的 QALYs 增加了 0.90 年,额外成本为 542,517.45 美元,导致 ICER 为 603,286.49 美元/QALY,超过了美国的意愿支付(WTP)阈值(150,000 美元)。单因素敏感性分析表明,疾病进展的效用、无进展生存的效用、塞普替尼的价格、折扣、培美曲塞的价格和帕博利珠单抗的价格对成本效益分析过程的影响最大。在 PSA 中,99.9%的散点分布在高于美国 WTP 阈值 150,000 美元的位置。
从美国支付者的角度来看,塞普替尼与化疗和帕博利珠单抗相比,用于治疗 RET 融合阳性 NSCLC 患者的一线治疗并不具有成本效益。