Cost-effectiveness of nivolumab plus ipilimumab as first-line therapy in advanced renal-cell carcinoma

Background Nivolumab plus ipilimumab improves overall survival and is associated with less toxicity compared with sunitinib in the first-line setting of advanced renal-cell carcinoma (RCC). The current study aimed to assess the cost-effectiveness of nivolumab plus ipilimumab for first-line treatment of advanced RCC from the payer perspectives high- and middle-income regions. Methods A decision-analytic model was constructed to evaluate the health and economic outcomes of first-line sunitinib and nivolumab plus ipilimumab treatment associated with advanced RCC. The clinical and utility data were obtained from published reports. The cost data were acquired for the payer perspectives of the United States (US), United Kingdom (UK), and China. Sensitivity analyses were performed to test the uncertainties of the results. Quality-adjusted life-years (QALYs) and incremental cost-effectiveness ratios (ICERs) were used. Results Nivolumab plus ipilimumab gained 0.70–0.76 QALYs compared with sunitinib. Our analysis determined the following ICERs for nivolumab plus ipilimumab over sunitinib in first-line advanced RCC treatment: US $ 85,506 /QALY; UK $ 126,499/QALY; and China $ 4682/QALY. Sensitivity analyses found the model outputs to be most affected for body weight and for the prices of nivolumab, sunitinib and ipilimumab. Conclusions Nivolumab plus ipilimumab as first-line treatment could gain more health benefits for advanced RCC in comparison with standard sunitinib, which is considered to be cost-effective in the US and China but not in the UK. Electronic supplementary material The online version of this article (10.1186/s40425-018-0440-9) contains supplementary material, which is available to authorized users.

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PID https://www.doi.org/10.1186/s40425-018-0440-9
PID pmc:PMC6247499
PID pmid:30458884
URL http://link.springer.com/article/10.1186/s40425-018-0440-9
URL https://www.ncbi.nlm.nih.gov/pubmed/30458884
URL http://link.springer.com/content/pdf/10.1186/s40425-018-0440-9.pdf
URL https://jitc.biomedcentral.com/track/pdf/10.1186/s40425-018-0440-9
URL https://link.springer.com/article/10.1186/s40425-018-0440-9
URL https://jitc.biomedcentral.com/articles/10.1186/s40425-018-0440-9
URL https://dx.doi.org/10.1186/s40425-018-0440-9
URL https://academic.microsoft.com/#/detail/2900705321
URL http://europepmc.org/articles/PMC6247499
URL https://jitc.bmj.com/content/6/1/124
URL https://jitc.bmj.com/content/jitc/6/1/124.full.pdf
URL http://link.springer.com/article/10.1186/s40425-018-0440-9/fulltext.html
URL https://doaj.org/toc/2051-1426
URL http://dx.doi.org/10.1186/s40425-018-0440-9
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Access Right Open Access
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Author Bin, Wu
Author Qiang, Zhang
Author Jie, Sun
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Collected From Europe PubMed Central; PubMed Central; UnpayWall; Datacite; DOAJ-Articles; Crossref; Microsoft Academic Graph
Hosted By Europe PubMed Central; Journal for ImmunoTherapy of Cancer
Journal Journal for Immunotherapy of Cancer, 6,
Publication Date 2018-11-20
Publisher BioMed Central
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Language English
Resource Type Other literature type; Article; UNKNOWN
system:type publication
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Source https://science-innovation-policy.openaire.eu/search/publication?articleId=dedup_wf_001::67ac07993c00bf0ba7e90aa79febfcfd
Author jsonws_user
Last Updated 26 December 2020, 16:53 (CET)
Created 26 December 2020, 16:53 (CET)