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Abstract Number: 1460

Effect of Guselkumab and IL-17 Inhibitors on Work Productivity and Activity Impairment in Psoriatic Arthritis: 6-Month Results of the PsABIOnd Observational Study

Stefan Siebert1, Mohamed Sharaf2, Frank Behrens3, Proton Rahman4, mitsumasa kishimoto5, Enrique R. Soriano6, Emmanouil Rampakakis7, László Köleséri8, Karissa Lozenski9, Ruben Queiro10, Ennio Lubrano11 and Laure Gossec12, 1University of Glasgow, Glasgow, United Kingdom, 2Janssen - Johnson & Johnson, Dubai, United Arab Emirates, 3Goethe-University & Fraunhofer ITMP, Frankfurt, Germany, 4Division of Rheumatology, Craig L. Dobbin Genetics Research Centre, Discipline of Medicine, Memorial University of Newfoundland, St. John's, Canada, 5Kyorin University School of Medicine, Tokyo, Japan, 6Rheumatology Section, Internal Medicine Service, Hospital Italiano de Buenos Aires and University Hospital Italiano de Buenos Aires, Buenos Aires, Argentina, 7JSS Medical Research, Montréal, QC, Canada, 8IQVIA, Budapest, Hungary, 9Johnson & Johnson, Horsham, PA, 10Hospital Universitario Central de Asturias, Oviedo. Asturias, Spain, 11Department of Medicine, Università deglia Studi del Molise, CAMPOBASSO, Italy, 12Sorbonne Universite and Pitie-Salpetriere Hospital, Paris, France

Meeting: ACR Convergence 2025

Keywords: Biologicals, Interleukins, Patient reported outcomes, Psoriatic arthritis

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Session Information

Date: Monday, October 27, 2025

Title: (1434–1466) Spondyloarthritis Including Psoriatic Arthritis – Treatment Poster II

Session Type: Poster Session B

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

Background/Purpose: Work impairment is a key issue in PsA. Biologic treatments can improve work status in patients (pts) with PsA; however, there is lack of comparative real-world data for different modes of action, e.g. IL-23 and IL-17 inhibitors (i). The current analysis aimed to assess PsA pt-reported outcomes (PRO), specifically work productivity, activity impairment, and disease impact after 6 months of treatment with guselkumab (GUS) and IL-17i.

Methods: PsABIOnd (NCT05049798) is a global (20 countries) observational study in PsA pts starting GUS or IL‑17i as 1st-to-4th line of biologic therapy per standard of care.1 Here, the full population of the PsABIOnd study was analyzed over the first 6 months of follow-up. Work productivity (overall work productivity loss, absenteeism, presenteeism) and activity impairment were assessed via the Work Productivity and Activity Impairment Questionnaire (WPAI; 0-100).2 Pt-reported disease impact was assessed using the PsA Impact of Disease-12 (PsAID‑12; 0-10),3 including the mean total score and proportions of pts achieving minimal clinically important improvement (MCII; improvement by ≥1.4; among pts with BL PsAID-12 score ≥1.4). All analyses were performed according to initial treatment group allocation and treatment comparison was based on 95% confidence intervals (CI).

Results: 1134 pts were analyzed; 555 and 579 received GUS or IL-17i, respectively, as their initial treatment. Mean age (53.2/53.5 yrs), sex (60.4%/59.2% female), and prior exposure to a targeted drug (63.4%/62.3%) were comparable for GUS/IL-17i. Mean overall baseline work productivity loss (42.3%/44.5% for GUS/IL17i groups), absenteeism (14.3%/12.9%), presenteeism (39.2%/42.1%), activity impairment (48.5%/50.6%), and mean baseline PsAID-12 total score (5.1/5.1) were also similar between groups.At the 6-month visit, comparable improvements were observed in all WPAI outcomes with GUS and IL-17i. Mean (95% CI) improvements in GUS/IL-17i were: overall work productivity loss (-13.1 [-16.5, -9.7]/-13.8 [-17.5, -10.1]%), absenteeism (-6.4 [-10.4, -2.4]/-2.5 [-5.1, 0.2]%), presenteeism (-12.5 [-15.7, -9.3]/-14.0 [-17.5, -10.5]%), activity impairment (-13.1 [-15.4, -10.8]/-15.7 [-18.2, -13.1]%; Fig 1). Mean PsAID-12 total scores also improved significantly (-1.6 [-1.7, -1.4]/-1.8 [-2.0, -1.6]) reaching levels (3.5/3.3) indicative of symptom impact below the pt acceptable symptom state threshold (≤ 4.0) in both groups (Fig 2). Rates of pts achieving PsAID-12 MCII at 6 months were also comparable (54.7%/55.9%).

Conclusion: By 6 months of treatment in real-world, improvements in work productivity and ability to perform daily activities were observed with both GUS and IL-17i which were paralleled with clinically meaningful improvements in pt-reported multidomain disease impact. Based on overlapping CIs, improvements in PROs were comparable between the two modes of action. These results may be useful for reimbursement decisions and healthcare provider/pt shared treatment decision-making.References1. Siebert S. Rheumatol Ther. 2023;10(2):4892. Teilly MC. Parmacoeconomics. 1993; 4(5):3533. Gossec L. Ann Rheum Dis. 2014;73(6):1012

Supporting image 1

Supporting image 2


Disclosures: S. Siebert: AbbVie, 6, Amgen, 6, AstraZeneca, 6, BMS, 5, Boehringer-Ingelheim, 5, Eli Lilly, 5, GlaxoSmithKlein, 5, Johnson & Johnson, 5, 6, Novartis, 6, Pfizer, 6, Syncona, 6, Teijin Pharma, 6, UCB, 5, 6; M. Sharaf: Johnson & Johnson, 3, 11; F. Behrens: AbbVie, 2, 6, BMS, 2, 6, Boehringer Ingelheim, 2, 6, Celgene, 2, 5, 6, Chugai, 2, 5, 6, Eli Lilly, 2, 6, Galapagos, 2, 6, Genzyme, 2, 6, Gilead, 2, 6, Johnson & Johnson, 2, 5, 6, MSD, 2, 6, Novartis, 2, 6, Pfizer, 2, 5, 6, Roche, 2, 5, 6, Sanofi, 2, 6, UCB, 2, 6; P. Rahman: Abbott, 2, AbbVie, 2, Amgen, 2, BMS, 2, Celgene, 2, Eli Lilly, 2, Janssen, 2, 5, Novartis, 2, 5, Pfizer, 2, UCB, 2; 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; E. Soriano: AbbVie, 5, 6, BMS, 5, 6, Eli Lilly, 5, 6, GSK, 5, 6, J&J, 5, 6, Novartis, 5, 6, Pfizer, 5, 6, Raffo, 5, 6, UCB, 5, 6; E. Rampakakis: Johnson & Johnson, 2, JSS Medical Research, 3; L. Köleséri: IQVIA, 3, Johnson & Johnson, 2; K. Lozenski: BMS, 11, Johnson & Johnson, 3, 11; R. Queiro: AbbVie, 2, 5, 6, Amgen, 2, 6, Celgene, 2, 6, Eli Lilly, 2, 6, Johnson & Johnson, 2, 5, 6, MSD, 2, 6, Novartis, 2, 5, 6, Pfizer, 2, 6; E. Lubrano: AbbVie, 6, Amgen, 6, Eli Lilly, 6, GlaxoSmithKlein, 6, Johnson & Johnson, 6, Novartis, 6, UCB, 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.

To cite this abstract in AMA style:

Siebert S, Sharaf M, Behrens F, Rahman P, kishimoto m, Soriano E, Rampakakis E, Köleséri L, Lozenski K, Queiro R, Lubrano E, Gossec L. Effect of Guselkumab and IL-17 Inhibitors on Work Productivity and Activity Impairment in Psoriatic Arthritis: 6-Month Results of the PsABIOnd Observational Study [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/effect-of-guselkumab-and-il-17-inhibitors-on-work-productivity-and-activity-impairment-in-psoriatic-arthritis-6-month-results-of-the-psabiond-observational-study/. Accessed .
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