As in rheumatoid arthritis, achieving low disease activity or remission in psoriatic arthritis (PsA) remains a challenge and unmet need for many individuals. However, the complex pathogenesis, heterogeneity and varied tissue involvement in PsA mean that dedicated definitions and novel solutions are required for difficult-to-treat disease.
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Acknowledgements
H.M.-O.’s work is supported by the National Institute for Health Research (NIHR) Leeds Biomedical Research Centre (LBRC). The views expressed are those of the authors and not necessarily those of the UK National Health Service, the NIHR, or the UK Department of Health. S.S. and H.M.-O. are co-leads for the planned EULAR task force to develop Points to Consider for the Definition of Difficult-to-treat PsA.
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S.S. declares that he has received institutional research support from Amgen, Boehringer Ingelheim, Bristol Myers Squibb, Eli Lilly, GSK, Janssen, Teijin Pharma and UCB and honoraria and/or speaker fees from AbbVie, Amgen, AstraZeneca, Eli Lilly, Janssen, Teijin Pharma and UCB. H.M.-O. declares that she has received research grants from Janssen, Novartis, Pfizer and UCB and honoraria and/or speaker fees from AbbVie, Amgen, Eli-Lilly, Janssen, Moonlake, Novartis, Pfizer, Takeda and UCB.
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Siebert, S., Marzo-Ortega, H. Difficult-to-treat psoriatic arthritis: moving out of the rheumatoid arthritis shadow. Nat Rev Rheumatol 20, 135–136 (2024). https://doi.org/10.1038/s41584-024-01083-y
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DOI: https://doi.org/10.1038/s41584-024-01083-y