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Cost-Effectiveness of Nivolumab in Recurrent Metastatic Head and Neck Squamous Cell Carcinoma
Mahdi Zargar1, Thomas McFarlane1,2, Kelvin K W Chan2,3,4
1University of Waterloo School of Pharmacy, Waterloo, Ontario, Canada.
Background:
Treatment options for patients with platinum-refractory, recurrent, metastatic head and neck squamous cell carcinoma (r/m HNSCC) are limited and prognosis is poor. The recent CheckMate 141 clinical trial demonstrated that nivolumab, an anti-programmed cell death protein 1 monoclonal antibody, was efficacious in extending the median overall survival (OS) in this patient population compared with standard therapies. We conducted a cost-effectiveness analysis to determine whether nivolumab is a cost-effective treatment in this patient population and examined various subgroups to determine for which, if any, the treatment is more cost-effective.
Materials And Methods:
We implemented a state transition model for HNSCC with a patient cohort who had tumor progression 6 months after the last dose of platinum-containing chemotherapy and compared the cost-effectiveness of nivolumab with docetaxel. Treatment effect estimates and adverse event rates were obtained from CheckMate 141. Costs, utilities, and other model inputs were gathered from published sources. We used a Canadian perspective, a 5-year time horizon, and a 1.5% discount rate for the analysis.
Results:
Nivolumab extended mean OS by 4 months compared with docetaxel and resulted in fewer treatment-related adverse events, producing an incremental effectiveness of 0.13 quality-adjusted life years (QALY). The incremental cost of treatment with nivolumab was $18,823. At a willingness-to-pay threshold of $100,000/QALY, nivolumab was not a cost-effective treatment option for r/m HNSCC, with an incremental cost-effectiveness ratio of $144,744/QALY. Nivolumab would be cost-effective if its price was reduced by 20%. Our subgroup analysis seemed to indicate that nivolumab might be cost-effective for tumors with expression of programmed death-ligand 1 >5%.
Conclusion:
We conclude that although nivolumab offers clinical benefit for the treatment of r/m HNSCC over current regimens, it is not cost-effective based on its list price. We have also established a value-based price estimate for nivolumab to be cost-effective in this patient population. Further study is required to draw a definitive conclusion on biomarkers for cost-effectiveness.
Implications For Practice:
In health care settings in which cost considerations are a constraint on choice of therapy, patient selection should be carefully considered to maintain efficiency in the system. Until a biomarker for response to therapy is identified for nivolumab, this medication is unlikely to be cost-effective for most patients with recurrent, metastatic head and neck squamous cell carcinoma.
Insights
Nivolumab offers clinical benefits for recurrent, metastatic head and neck squamous cell carcinoma (r/m HNSCC) but is not cost-effective at its current price. Cost-effectiveness may be achieved with a price reduction or for patients with high programmed death-ligand 1 expression.
Area of Science:
- Oncology
- Health Economics
- Pharmacoeconomics
Background:
- Limited treatment options and poor prognosis exist for platinum-refractory, recurrent, metastatic head and neck squamous cell carcinoma (r/m HNSCC).
- Nivolumab, an anti-programmed cell death protein 1 (PD-1) antibody, demonstrated improved overall survival (OS) in the CheckMate 141 trial for this patient population.
- Cost-effectiveness of nivolumab compared to standard therapies in r/m HNSCC requires evaluation.
Purpose of the Study:
- To determine the cost-effectiveness of nivolumab versus docetaxel for treating platinum-refractory, recurrent, metastatic head and neck squamous cell carcinoma (r/m HNSCC).
- To identify patient subgroups for whom nivolumab may be more cost-effective.
Main Methods:
- A state transition model was developed for HNSCC patients progressing after platinum chemotherapy.
- Treatment effects and adverse events were sourced from the CheckMate 141 trial.
- A Canadian perspective, 5-year time horizon, and 1.5% discount rate were applied.
Main Results:
- Nivolumab extended mean OS by 4 months and improved quality-adjusted life years (QALYs) by 0.13 compared to docetaxel.
- The incremental cost-effectiveness ratio (ICER) for nivolumab was $144,744/QALY, exceeding the $100,000/QALY willingness-to-pay threshold.
- Nivolumab could be cost-effective with a 20% price reduction or for patients with programmed death-ligand 1 (PD-L1) expression >5%.
Conclusions:
- Nivolumab provides clinical benefits for r/m HNSCC but is not cost-effective at its current list price.
- A value-based price estimate suggests potential cost-effectiveness with price adjustments.
- Further research is needed to identify reliable biomarkers for nivolumab cost-effectiveness.
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