AUTHOR=Hu Huabin , She Longjiang , Liao Mengting , Shi Yin , Yao Linli , Ding Dong , Zhu Youwen , Zeng Shan , Carbone David P. , Huang Jin TITLE=Cost-Effectiveness Analysis of Nivolumab Plus Ipilimumab vs. Chemotherapy as First-Line Therapy in Advanced Non-Small Cell Lung Cancer JOURNAL=Frontiers in Oncology VOLUME=Volume 10 - 2020 YEAR=2020 URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2020.01649 DOI=10.3389/fonc.2020.01649 ISSN=2234-943X ABSTRACT=ABSTRACT Background: 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). Methods: A Markov model was developed to estimate cost and effectiveness of nivolumab plus ipilimumab versus chemotherapy as the first-line therapy in patients with advanced NSCLC based on outcomes data from the CheckMate 227 trial. Cost and health outcomes were estimated at a willingness-to-pay (WTP) threshold of $150000 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. Results: The incremental costs and QALYs that nivolumab plus ipilimumab yielded, compared with chemotherapy, 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%, leading 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 provided an additional 2.04 QALYs, at a cost of $69182.50 per QALY. Conclusion: Nivolumab plus ipilimumab as first-line therapy is a cost-effective strategy compared with chemotherapy in advanced NSCLC patients with PD-L1 expression levels ≥50% and ≥1% or a high TMB, at a willingness-to-pay threshold of $150000 per QALY, but not in the patients with a PD-L1 expression <1%.