Projected increases of cancer-attributable health-care costs, accompanied by staff shortages, will impose future economic and operational challenges on national health-care systems. Herein, we highlight a series of clinical and health economic rationales in support of publicly funded clinical trial teams that conduct real-world dose-reduction trials aiming for adjustment of cancer drug label doses to reduce not only the financial burden on payers, but also the toxicity burden on patients.
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Acknowledgements
The work of K.T.M. is supported by a Novo Nordisk Foundation clinical research fellowship (grant no. 100191) and centre grant (Novo Nordisk Foundation Center for Stem Cell Biology, DanStem, grant no. NNF17CC0027852), by the Danish Council for Strategic Research (grant no. 2034-00089B), the Danish Cancer Society (grant no. R302-A17376), Børnecancerfonden (2021-7385), the Danish Health Regions, and the Sven Andersen Fonden. The work of L.E. is supported by Nordic Institute of Health Economics A/S.
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Theilgaard-Mönch, K., Ehlers, L.H. Dose-reduction trials in oncology — aiming for less toxicity and better quality of life at lower costs. Nat Rev Clin Oncol 21, 81–82 (2024). https://doi.org/10.1038/s41571-023-00831-5
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DOI: https://doi.org/10.1038/s41571-023-00831-5