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Abstract Number: 2339

Joint Groups Involved in Early Oligoarticular Psoriatic Arthritis and the Impact of Apremilast Treatment: Data From FOREMOST

Alen Zabotti1, Joseph F Merola2, Ulrich Mrowietz3, Philip J. Mease4, Laure Gossec5, mitsumasa kishimoto6, Michele Brunori7, Lichen Teng8, Dafna D. Gladman9 and Laura Coates10, 1Division of Rheumatology, Department of Medicine (DMED), Academic Hospital "Santa Maria della Misericordia", ASUFC, University of Udine, Udine, Italy, Udine, Italy, 2Department of Dermatology and Department of Medicine, UT Southwestern Medical Center, Dallas, TX, 3Department of Dermatology, University Medical Center Schleswig-Holstein, Kiel, Germany, 4Department of Rheumatology, Providence-Swedish Medical Center and University of Washington, Seattle, WA, 5Sorbonne Universite and Pitie-Salpetriere Hospital, Paris, France, 6Kyorin University School of Medicine, Tokyo, Japan, 7Amgen Inc, Zurich, Switzerland, 8Amgen Inc., Thousand Oaks, 9Schroeder Arthritis Institute, Krembil Research Institute, Toronto Western Hospital, Division of Rheumatology, Toronto, ON, Canada, 10Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, England, United Kingdom

Meeting: ACR Convergence 2025

Keywords: Psoriatic arthritis, Randomized Trial

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Session Information

Date: Tuesday, October 28, 2025

Title: (2338–2376) Spondyloarthritis Including Psoriatic Arthritis – Treatment Poster III

Session Type: Poster Session C

Session Time: 10:30AM-12:30PM

Background/Purpose: Data on disease progression and joint involvement patterns in early oligoarticular (oligo) PsA are sparse. In the FOREMOST study (NCT03747939), apremilast (APR) decreased the number of involved joints vs placebo (PBO) at Week (Wk) 16.1 We assess patterns of involved joints at baseline and effect of APR on joint groups through Wk 48.

Methods: FOREMOST enrolled 308 patients (pts) with early oligo PsA ( >1–≤4 swollen, >1–≤4 tender joints; 66–68 joints assessed). Pts were randomized 2:1 to APR (n=203) or PBO (n=105) for 24 wks (early escape at Wk 16), after which all pts received APR through Wk 48. Overall, 291 pts received ≥1 dose of APR (as randomized, n=203; switched from PBO, n=88). Concomitant NSAIDs and/or synthetic DMARDs were permitted at a stable dose for ≥2 wks or ≥3 months before baseline, respectively, and maintained through Wk 24. For each joint group (Table 1), percentage of pts (pt incidence) with ≥1 of the following was calculated at baseline, Wks 16 and 48: swollen and tender, swollen and/or tender, swollen only, and tender only. Baseline and Wk 16 data were analyzed for all randomized pts with the last observation carried forward for missing data; Wk 48 data were analyzed as observed for pts who received ≥1 dose of APR.

Results: Pts had low baseline joint involvement: mean swollen and tender joint count, 2.6 and 3.2, respectively;1 baseline pt incidence of “swollen and tender” and “swollen and/or tender” joints was similar and higher than “swollen only” and “tender only” (Fig 1A). Based on “swollen and tender” joints, the most commonly involved joint groups at baseline included large and small joints: finger PIP (39.0% pts with ≥1 involved joint) and MCP (33.1%), followed by knee (19.8%), and ankle and tarsus/midfoot (18.8%) (Fig 1A). Baseline patterns of swollen and tender joints were similar for APR and PBO (Fig 1B). Greater improvements in swollen and tender finger PIP, MCP, knee and ankle/tarsus/midfoot joints were observed from baseline to Wk 16 for APR vs PBO: finger PIP, –23.6% vs –9.5% pt incidence; MCP, –21.7% vs –13.3%; knee –16.3% vs +2.9%; and ankle/tarsus/midfoot, –12.3% vs –8.6% (Fig. 1B, C). Across joint groups, risk of ≥1 swollen and tender joint at Wk 16 was lower for APR vs PBO (Fig. 1D), with significant differences observed for the most commonly involved joints: odds ratio (APR vs PBO) (95% CI) for finger PIP, 0.55 (0.31, 0.98); MCP, 0.51 (0.27, 0.97); knee, 0.33 (0.16, 0.71); ankle/tarsus/midfoot, 0.41 (0.17, 0.94) (Fig. 1D). Improvements in joint involvement observed with APR at Wk 16 were maintained in pts continuing or switching to APR through Wk 48.

Conclusion: Our data indicate a mix of large and small joints involved in early oligo PsA, with hand and finger most common. We observed similar joint patterns as reported at PsA onset in real-world cohorts,2,3 underscoring the value of FOREMOST in understanding early oligo PsA. Compared with PBO, APR significantly reduced joint involvement across large and small joints. Our findings can help orient physicians treating early oligo PsA.References: 1 Gossec. Ann Rheum Dis. 2024;83(11):1480-14882 Zabotti. RMD Open. 2024;10(2):e004314 3 Gladman. J Rheumatol. 2021;48(12):1824-1829

Supporting image 1Table 1. Joint groups analyzed

Supporting image 2Figure 1. Joint involvement in the FOREMOST study of early oligoarticular PsA


Disclosures: A. Zabotti: AbbVie/Abbott, 2, 5, Amgen, 2, 5, Eli Lilly, 2, 5, Johnson & Johnson, 2, 5, 6, Novartis, 2, 5, UCB, 2, 5; J. Merola: AbbVie, 2, Amgen, 2, 5, AstraZeneca, 2, 5, Biogen, 2, 5, Boehringer Ingelheim, 2, 5, Bristol Myers Squibb, 2, 5, Dermavant, 2, 5, Eli Lilly and Company, 2, 5, Incyte, 2, Janssen, 2, 5, LEO Pharma, 2, MoonLake Immunotherapeutics, 2, 5, Novartis, 2, Pfizer, 2, Sanofi-Regeneron, 2, 5, Sun Pharma, 5, UCB, 2, 5; U. Mrowietz: AbbVie, 1, 5, 6, Aditxt, 1, Almirall, 1, Amgen, 1, Biogen, 1, Boehringer-Ingelheim, 1, Bristol-Myers Squibb(BMS), 1, Eli Lilly, 1, Immunic Therapeutics, 1, Janssen-Cilag, 1, LEO Pharma, 1, Merck/MSD, 1, Novartis, 1, Phi-Stone, 1, selectION, 1, Sharp & Dohme, 1, 5, 6, UCB, 1, UNION therapeutics, 1, 5, 6; P. Mease: AbbVie, 2, 5, 6, Acelyrin, 2, 5, Amgen, 2, 5, 6, BMS, 2, 5, Century, 2, Cullinan, 2, Eli Lilly and Company, 2, 5, 6, Inmagene, 2, J&J Innovative Medicine, 2, 5, 6, MoonLake Immunotherapeutics, 2, Novartis, 2, 5, 6, Pfizer, 2, 5, 6, Sana, 5, Spyre, 5, Takeda, 2, UCB, 2, 5, 6; L. Gossec: AbbVie, 2, 5, Amgen, 2, Biogen, 5, BMS, 2, Celltrion, 2, Eli Lilly, 2, 5, Janssen, 2, MSD, 2, Novartis, 2, 5, Pfizer, 2, UCB, 2, 5; m. kishimoto: AbbVie, 2, 6, Amgen, 2, 6, Asahi-Kasei Pharma, 2, 6, Astellas, 2, 6, Ayumi, 2, 6, BMS, 2, 6, Celgene, 2, 6, Chugai, 2, 6, Daiichi-Sankyo, 2, 6, Eisai, 2, 6, Eli Lilly, 2, 6, Gilead, 2, 6, Johnson & Johnson, 2, 6, Kyowa Kirin, 2, 6, Novartis, 2, 6, Ono Pharma, 2, 6, Takeda, 2, 6, Tanabe-Mitsubishi, 2, 6, UCB, 2, 6; M. Brunori: Amgen, 3; L. Teng: Amgen Inc., 3, 11; D. Gladman: AbbVie, 2, 5, Amgen, 2, 5, AstraZeneca, 2, BMS, 2, 5, Eli Lilly, 2, 5, Janssen, 5, Johnson & Johnson, 2, Novartis, 2, 5, Pfizer, 2, 5, Roche, 2, UCB, 2, 5; L. Coates: AbbVie, 2, 5, 6, Amgen, 2, 5, 6, Biogen, 6, BMS, 2, Boehringer Ingelheim, 2, Celgene, 2, 5, 6, Domain, 2, Eli Lilly and Company, 2, 5, 6, Galapagos, 2, 6, Gilead, 2, 5, 6, GSK, 6, Janssen, 2, 5, 6, Medac, 6, MoonLake Immunotherapeutics, 2, Novartis, 2, 5, 6, Pfizer, 2, 5, 6, UCB, 2, 5, 6.

To cite this abstract in AMA style:

Zabotti A, Merola J, Mrowietz U, Mease P, Gossec L, kishimoto m, Brunori M, Teng L, Gladman D, Coates L. Joint Groups Involved in Early Oligoarticular Psoriatic Arthritis and the Impact of Apremilast Treatment: Data From FOREMOST [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/joint-groups-involved-in-early-oligoarticular-psoriatic-arthritis-and-the-impact-of-apremilast-treatment-data-from-foremost/. Accessed .
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