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Review
. 2024 Nov;25(11):e611-e616.
doi: 10.1016/S1470-2045(24)00212-2. Epub 2024 Oct 14.

Interchangeability of immune checkpoint inhibitors: an urgent need for action

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Review

Interchangeability of immune checkpoint inhibitors: an urgent need for action

Michiel Zietse et al. Lancet Oncol. 2024 Nov.

Abstract

Prevailing uncertainties regarding the therapeutic interchangeability of PD-1 and PD-L1 inhibitors affect both clinical decision making and health-care budgeting. This Personal View presents a comprehensive assessment of the fragmented regulatory landscape of PD-1 and PD-L1 inhibitors, highlighting the complex dynamics of market competition, pricing, and the effect on health-care budgets. Our paper explores the current state of clinical trials, uninformative trial designs, and the challenges they pose in evaluating the therapeutic interchangeability of these drugs. To address these challenges, research that will inform us of the extent of interchangeability of PD-1 and PD-L1 inhibitors is needed. We recommend head-to-head randomised controlled trials, standardised study designs for indirect comparisons, trials with monotherapy groups, post-approval trials funded from private or public sources, and adoption of a near-equivalence framework in both conducting and evaluating trials.

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Conflict of interest statement

Declaration of interests RWFvL reports research grants (all paid to their institution) from Bristol Myers Squibb and Pfizer; received consulting fees from Bristol Myers Squibb, Roche, Pierre Fabre, AstraZeneca, and Pfizer; received speaker fees from AstraZeneca; and declares travel support from Ipsen, all outside the submitted work. SBvWvD-K reports a research grant (paid to their institution) for PRIME-ROSE (grant number 101104269); and received travel support from the European Medicines Agency, Nordic Precision Medicine Forum, Centre for Innovation in Regulatory Science, and Cancer Drug Development Forum, all outside the submitted work. RHJM reports unrestricted research grants (all paid to their institution) from Astellas, Bayer, Boehringer ngelheim, Cristal Therapeutics, Deuter Oncology, Novartis, Nordic Pharma, Pamgene, Pfizer, Roche, Sanofi, and Servier, all outside the submitted work. All other authors declare no competing interests.

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