Journal
CLINICAL ONCOLOGY
Volume 34, Issue 3, Pages E123-E129Publisher
ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.clon.2021.10.008
Keywords
Cemiplimab; chemotherapy; cost-effectiveness analysis; NSCLC; PD-L1
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The study evaluated the cost-effectiveness of cemiplimab versus chemotherapy in treating NSCLC in the US. The results showed that cemiplimab significantly prolonged the progression-free survival and overall survival of patients compared to chemotherapy, but at an additional cost. The cost-effectiveness analysis indicated that cemiplimab is a cost-effective option for first-line treatment in NSCLC patients with at least 50% PD-L1 positivity from an American perspective.
Aims: The EMPOWER-Lung 1 trial showed that cemiplimab significantly prolongs the duration of progression-free survival and overall survival in advanced non -small cell lung cancer (NSCLC) patients with at least 50% programmed cell death receptor ligand-1 (PD-L1) positivity, yet the financial burden may limit its use. The aim of the present study was to evaluate the cost-effectiveness of cemiplimab versus chemotherapy in a US setting. Materials and methods: A Markov model, with three mutually exclusive health states, was used to compare the expected health outcomes and cost of cemi-plimab with chemotherapy. Survival data and transition probabilities were collected from the EMPOWER-Lung 1 trial. Utility values and costs are publicly available from open sources. One-way and probabilistic sensitivity analyses were conducted in both the whole population and subgroups to test the robustness of the parameters and structure. Results: Treatment of NSCLC with cemiplimab yielded an extra 1.07 quality-adjusted life years (QALYs) at an additional cost of $98 211 compared with chemotherapy, associated with an incremental cost-effectiveness ratio of $91 891/QALY and an incremental net health benefit of 0.087 QALYs at a willingness to pay threshold of $100 000/QALY. The probabilistic sensitivity analysis indicated that cemiplimab provided an 83.2% probability of being cost-effective. One-way sensitivity analysis suggested that the price of cemiplimab was the chief driver in this model. A subgroup analysis showed that cemiplimab was the preferred incremental net health benefit in more than half of the subgroups, including patients with squamous type disease and metastases. Conclusions: Cemiplimab is a cost-effective option in the first-line treatment of NSCLC in patients who are at least 50% PD-L1 positive from an American perspective. (c) 2021 The of Published Elsevier Ltd. All reserved.
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