Hu Huabin, She Longjiang, Liao Mengting, Shi Yin, Yao Linli, Ding Dong, Zhu Youwen, Zeng Shan, Carbone David P, Huang Jin
Department of Medical Oncology, The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangdong Institute of Gastroenterology, Guangzhou, China.
Front Oncol. 2020 Sep 8;10:1649. doi: 10.3389/fonc.2020.01649. eCollection 2020.
The CheckMate 227 trial has indicated that nivolumab plus ipilimumab compared with chemotherapy significantly increases long-term survival in the first-line setting of advanced non-small-cell lung cancer (NSCLC). A Markov model was built to estimate the cost and effectiveness of nivolumab plus ipilimumab vs. chemotherapy as the first-line therapy in patients with advanced NSCLC based on outcomes data from the CheckMate 227 trial. We calculated the cost and health outcomes at a willingness-to-pay (WTP) threshold of $150,000 per quality adjusted life year (QALY) in populations with different programmed death ligand 1 (PD-L1) expression levels (≥50, ≥1, and <1%) or a high tumor mutational burden (TMB) (≥10 mutations per megabase). Sensitivity analysis were used to test the model stability. The outcomes showed that the incremental costs and QALYs by using nivolumab plus ipilimumab were $124180.76 and 1.16, $70951.42 and 0.53, $144093.63 and 0.83 for the advanced NSCLC patients with a PD-L1 expression ≥50%, ≥1%, and <1%, which led to an incremental cost-effective ratio (ICER) of $107403.72, $133732.20, and $172589.15 per QALY, respectively. For patients with a high TMB, nivolumab plus ipilimumab contributed an extra 2.04 QALYs at a cost of $69182.50 per QALY. Nivolumab plus ipilimumab as first-line therapy makes a better cost-effective strategy than chemotherapy in advanced NSCLC patients with PD-L1 expression levels ≥50% and ≥1% or a high TMB, at a willingness-to-pay threshold of $150,000 per QALY, but not in the patients with a PD-L1 expression <1%.
CheckMate 227试验表明,在晚期非小细胞肺癌(NSCLC)一线治疗中,纳武利尤单抗联合伊匹木单抗与化疗相比可显著提高长期生存率。基于CheckMate 227试验的结果数据,构建了一个马尔可夫模型,以评估纳武利尤单抗联合伊匹木单抗与化疗作为晚期NSCLC患者一线治疗的成本和效果。我们在不同程序性死亡配体1(PD-L1)表达水平(≥50%、≥1%和<1%)或高肿瘤突变负荷(TMB)(每兆碱基≥10个突变)的人群中,以每质量调整生命年(QALY)150,000美元的支付意愿(WTP)阈值计算成本和健康结果。采用敏感性分析来检验模型的稳定性。结果显示,对于PD-L1表达≥50%、≥1%和<1%的晚期NSCLC患者,使用纳武利尤单抗联合伊匹木单抗的增量成本和QALY分别为124180.76美元和1.16、70951.42美元和0.53、144093.63美元和0.83,导致每QALY的增量成本效益比(ICER)分别为107403.72美元、133732.20美元和172589.15美元。对于高TMB患者,纳武利尤单抗联合伊匹木单抗每QALY成本为69182.50美元,可额外增加2.04个QALY。在每QALY支付意愿阈值为150,000美元时,对于PD-L1表达水平≥50%和≥1%或高TMB的晚期NSCLC患者,纳武利尤单抗联合伊匹木单抗作为一线治疗比化疗具有更好的成本效益策略,但对于PD-L1表达<1%的患者则不然。