Camrelizumab in patients with advanced non-squamous non-small cell lung cancer: a cost-effective analysis in China.
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Where this comes from
- Record sourced from PubMed, PMID 36194670.
- Also identified by DOI 10.1136/bmjopen-2022-061592 and PMC identifier 9362787.
- Licence recorded as CC BY-NC.
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Abstract
Camrelizumab is a selective, humanised, high-affinity IgG<sub>4</sub> kappa monoclonal antibody against programmed cell death 1 that shows effective antitumour activity with acceptable toxicity in multiple tumour types. The CameL trial demonstrated that camrelizumab plus chemotherapy (CC) significantly prolonged the median progression-free survival and median overall survival versus chemotherapy alone (CA) in patients with advanced non-squamous non-small cell lung cancer (NSCLC). Our study was conducted to investigate the cost-effectiveness of the two strategies in chemotherapy-naive patients with advanced non-squamous NSCLC. A Markov simulation model was generated based on the CameL trial. The two simulated treatments included CC and CA. Utility was derived from published literature, and costs were calculated based on those at our hospital in Chengdu, China. Incremental cost-effectiveness ratios (ICERs) were calculated to compare the cost-effectiveness of the two treatment arms. In the overall population, the total costs were $27 223.40 and $13 740.10 for CC and CA treatment, respectively. The CC treatment produced 1.37 quality-adjusted life years (QALYs), and the CA treatment produced 1.17 QALYs. Hence, patients who were in the CC group spent an additional $13 483.30 and generated an increase of 0.20 QALYs, resulting in an ICER of $67 416.50 per QALY. For chemotherapy-naive patients with advanced non-squamous NSCLC, CC is not considered a cost-effective treatment versus CA in China when considering a willingness-to-pay threshold of $31 500 per QALY. NCT03134872.
Medical subject headings
- Carcinoma, Non-Small-Cell Lung
- Lung Neoplasms