Merck & Co., Inc., 126 East Lincoln Ave., P.O. Box 2000, Rahway, NJ, 07065, USA.
Analysis Group, Inc., Boston, MA, USA.
Adv Ther. 2023 Jul;40(7):3038-3055. doi: 10.1007/s12325-023-02525-x. Epub 2023 May 16.
Pembrolizumab was approved in the US as adjuvant treatment of patients with stage IIB or IIC melanoma post-complete resection, based on prolonged recurrence-free survival vs. placebo in the Phase 3 KEYNOTE-716 trial. This study aimed to evaluate the cost-effectiveness of pembrolizumab vs. observation as adjuvant treatment of stage IIB or IIC melanoma from a US health sector perspective.
A Markov cohort model was constructed to simulate patient transitions among recurrence-free, locoregional recurrence, distant metastasis, and death. Transition probabilities from recurrence-free and locoregional recurrence were estimated via multistate parametric modeling based on patient-level data from an interim analysis (data cutoff date: 04-Jan-2022). Transition probabilities from distant metastasis were based on KEYNOTE-006 data and network meta-analysis. Costs were estimated in 2022 US dollars. Utilities were based on applying US value set to EQ-5D-5L data collected in trial and literature.
Compared to observation, pembrolizumab increased total costs by $80,423 and provided gains of 1.17 quality-adjusted life years (QALYs) and 1.24 life years (LYs) over lifetime, resulting in incremental cost-effectiveness ratios of $68,736/QALY and $65,059/LY. The higher upfront costs of adjuvant treatment were largely offset by reductions in costs of subsequent treatment, downstream disease management, and terminal care, reflecting the lower risk of recurrence with pembrolizumab. Results were robust in one-way sensitivity and scenario analyses. At a $150,000/QALY threshold, pembrolizumab was cost-effective vs. observation in 73.9% of probabilistic simulations that considered parameter uncertainty.
As an adjuvant treatment of stage IIB or IIC melanoma, pembrolizumab was estimated to reduce recurrence, extend patients' life and QALYs, and be cost-effective versus observation at a US willingness-to-pay threshold.
基于 KEYNOTE-716 三期临床试验中无复发生存期较安慰剂延长,帕博利珠单抗(pembrolizumab)获美国批准用于完全切除后的 IIB 期或 IIC 期黑色素瘤患者的辅助治疗。本研究旨在从美国卫生部门的角度评估帕博利珠单抗对比观察作为 IIB 期或 IIC 期黑色素瘤辅助治疗的成本效益。
构建了一个马尔可夫队列模型,以模拟无复发生存期、局部区域复发、远处转移和死亡患者的转移。无复发生存期和局部区域复发的转移概率通过基于患者水平数据的多状态参数建模进行估计(数据截止日期:2022 年 1 月 4 日)。远处转移的转移概率基于 KEYNOTE-006 数据和网络荟萃分析。成本以 2022 年美元计。效用基于将美国值集应用于试验和文献中收集的 EQ-5D-5L 数据得出。
与观察相比,帕博利珠单抗的总费用增加了 80423 美元,终生提供了 1.17 个质量调整生命年(QALY)和 1.24 个生命年(LY)的增益,增量成本效益比为 68736 美元/QALY 和 65059 美元/LY。辅助治疗的前期成本较高,但随后的治疗、下游疾病管理和终末期护理成本降低,很大程度上抵消了这一成本,这反映了帕博利珠单抗降低了复发风险。单因素敏感性分析和情景分析结果稳健。在 15 万美元/QALY 的阈值下,考虑到参数不确定性,在 73.9%的概率模拟中,帕博利珠单抗对比观察具有成本效益。
作为 IIB 期或 IIC 期黑色素瘤的辅助治疗,帕博利珠单抗可降低复发风险,延长患者的生存时间和 QALY,且在符合美国意愿支付阈值的情况下具有成本效益。