Centre for Observational and Real-world Evidence, Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, 07033, USA.
Department of Hematology and Oncology, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 27710, USA.
Pharmacoeconomics. 2017 Aug;35(8):831-844. doi: 10.1007/s40273-017-0527-z.
Our objectives were to evaluate the cost effectiveness of pembrolizumab compared with standard-of-care (SoC) platinum-based chemotherapy as first-line treatment in patients with metastatic non-small-cell lung cancer (NSCLC) that expresses high levels of programmed death ligand-1 (PD-L1) [tumour proportion score (TPS) ≥50%], from a US third-party public healthcare payer perspective.
We conducted a partitioned-survival model with a cycle length of 1 week and a base-case time horizon of 20 years. Parametric models were fitted to Kaplan-Meier estimates of time on treatment, progression-free survival and overall survival from the KEYNOTE-024 randomized clinical trial (patients aged ≥18 years with stage IV NSCLC, TPS ≥50%, without epidermal growth factor receptor (EGFR)-activating mutations or anaplastic lymphoma kinase (ALK) translocations who received no prior systemic chemotherapy) and validated with long-term registry data. Quality-adjusted life-years (QALYs) were calculated based on EuroQoL-5 Dimensions (EQ-5D) utility data collected in the trial. Costs ($US, year 2016 values) for drug acquisition/administration, adverse events and clinical management were included. Costs and outcomes were discounted at 3% per year. A series of deterministic and probabilistic sensitivity analyses were performed to test the robustness of the results.
In the base-case scenario, pembrolizumab resulted in an expected gain of 1.31 life-years (LYs) and 1.05 QALYs and an incremental cost of $US102,439 compared with SoC. The incremental cost per QALY gain was $US97,621/QALY and the incremental cost per LY gain was $US78,344/LY.
Pembrolizumab is projected to be a cost-effective option compared with SoC platinum-based chemotherapy as first-line treatment in adults with metastatic NSCLC expressing high levels of PD-L1.
我们的目标是从美国第三方公共医疗支付者的角度评估派姆单抗(pembrolizumab)对比标准护理(SoC)含铂化疗作为高表达程序性死亡配体 1(PD-L1)[肿瘤比例评分(TPS)≥50%]的转移性非小细胞肺癌(NSCLC)患者一线治疗的成本效果。
我们使用分割生存模型,其周期长度为 1 周,基本情况时间范围为 20 年。我们使用 KEYNOTE-024 随机临床试验(年龄≥18 岁、IV 期 NSCLC、TPS≥50%、无表皮生长因子受体(EGFR)激活突变或间变性淋巴瘤激酶(ALK)易位且未接受过系统化疗的患者)的Kaplan-Meier 治疗时间、无进展生存期和总生存期估计值拟合参数模型,并通过长期登记数据进行验证。根据试验中收集的 EuroQoL-5 维度(EQ-5D)效用数据计算质量调整生命年(QALY)。纳入药物获取/管理、不良事件和临床管理的成本($US,2016 年值)。成本和结果每年贴现 3%。进行了一系列确定性和概率敏感性分析,以检验结果的稳健性。
在基本情况假设下,与 SoC 相比,派姆单抗预计可增加 1.31 个生命年(LY)和 1.05 个 QALY,增量成本为 102439 美元。增量成本每获得一个 QALY 为 97621 美元,增量成本每获得一个 LY 为 78344 美元。
与 SoC 含铂化疗相比,派姆单抗作为高 PD-L1 表达的转移性 NSCLC 成人一线治疗方案,预计具有成本效益。