Abstract
Discovery and clinical development of monoclonal antibodies with the ability to interfere in the regulation of the immune response have significantly changed the landscape of oncology in recent years. Among the active agents licensed by the regulatory agencies, nivolumab and pembrolizumab are paradigmatic as the most relevant ones according to the magnitude of available data derived from the extensive preclinical and clinical experience. Although in both cases the respective data sheets indicate well-defined dosage regimens, a review of the literature permits to verify the existence of many issues still unresolved about dosing the two agents, so it must be considered an open question of potentially important consequences, in which to work to improve the effectiveness and efficiency of use.
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MS has conceived the work and drafted the paper. EC has made substantial contributions to the design of the work and drafted the paper. JJM has substantively contributed to the design. VE-O has made substantial contributions to the design of the work and drafted the paper. EM-N has substantively revised the work. AC has substantively revised the work. JR has made substantial contributions and drafted the paper. All authors have approved the submitted version and are personally accountable for the author's own contributions and they ensure that questions related to the accuracy or integrity of any part of the work, even ones in which the author was not personally involved, are appropriately investigated, resolved, and the resolution documented in the literature.
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Manuel Sureda has received travel grants from Bristol Myers and MSD. Juan José Mata has received travel grants from Bristol Myers. The other authors have no conflicts of interest to disclose.
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Sureda, M., Calvo, E., Mata, J.J. et al. Dosage of anti-PD-1 monoclonal antibodies: a cardinal open question. Clin Transl Oncol 23, 1511–1519 (2021). https://doi.org/10.1007/s12094-021-02563-3
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DOI: https://doi.org/10.1007/s12094-021-02563-3