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Abstract Number: 1878

Customized Therapy for SLE: How Disease Severity Influences the Use of Corticosteroids and Biologics in Patients with SLE in the Lupus Federated Data Network (LupusNet) and a US Claims Database

Ashley Orillion1, Federico Zazzetti2, Anna Sheahan3, Clair Blacketer1, Michel van Speybroeck4, Sarah Gasman1, Reyhan Sonmez5, Erika Noss1, Manuel Ugarte-Gil6, Rocío Gamboa-Cárdenas7, Víctor Pimentel-Quiroz8, Kaleb Michaud9, Patti Katz10, Rangi Kandane-Rathnayake11, Eric Morand12, Worawit Louthrenoo13, Alberta Hoi14, Yi-Hsing Chen15, Jiacai Cho16, Laniyati Hamijoyo17, Shue Fen Luo18, Sandra Navarra19, Mandana Nikpour20, José María Pego-Reigosa21, Iñigo Rúa-Figueroa22, Zulema Plaza23, María Galindo-Izquierdo24, Julia Martínez Barrio25, Jaime Calvo26, Antonio Fernández-Nebro27, Raúl Menor Almagro28, EVA GLORIA TOMERO MURIEL29, Javier Narváez30 and Chetan S. Karyekar31, 1Johnson & Johnson, Spring House, PA, USA, Spring House, PA, 2Johnson & Johnson, Horsham, PA, USA, Ambler, PA, 3Johnson & Johnson, Horsham, PA, USA, Horhsam, PA, 4Johnson & Johnson, Beerse, Belgium, Beerse, Belgium, 5Capgemini Consulting, Zurich, Switzerland, Zurich, Switzerland, 6Grupo Peruano de Estudio de Enfermedades Autoinmunes Sistémicas, Universidad Científica del Sur, Lima, Peru; Hospital Guillermo Almenara Irigoyen, EsSalud, Lima, Peru, Lima, Peru, 7Universidad Científica del Sur, Lima, Peru, 8Grupo Peruano de Estudio de Enfermedades Autoinmunes Sistémicas, Universidad Científica del Sur, Lima, Perú; Rheumatology Department, Hospital Guillermo Almenara Irigoyen, EsSalud, Lima, Perú, Lima, Peru, 9University of Nebraska Medical Center, Omaha, NE, 10UCSF, San Rafael, CA, 11Center for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia, 12Centre for Inflammatory Diseases, Monash University and Monash Health, Melbourne, Victoria, Australia, 13Chiang Mai University Hospital, Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Chiang Mai, Thailand, Chiang Mai, Thailand, 14Centre for Inflammatory Diseases, Monash University and Department of Rheumatology, Monash Health, Clayton, Victoria, Australia, 15Taichung Veterans General Hospital, Division of Allergy, Immunology and Rheumatology, Taichung, Taiwan, Taichung, Taiwan (Republic of China), 16National University Hospital, Rheumatology Division, Department of Medicine, Singapore, Singapore, Singapore, Singapore, 17Padjadjaran University/Hasan Sadikin General Hospital, Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Bandung, Indonesia, Badung, Indonesia, 18Chang Gung Memorial Hospital, Chang Gung University, Department of Rheumatology, Allergy and Immunology, Taipei, Taiwan, Taoyuan, Taiwan (Republic of China), 19University of Santo Tomas, Manila, Philippines, 20University of Sydney, School of Public Health, Faculty of Medicine and Health, Sydney, New South Wales, Australia; St Vincent’s Hospital Melbourne, Department of Rheumatology, Fitzroy, Victoria, Australia, Melbourne, Victoria, Australia, 21Department of Rheumatology, University Hospital of Vigo, Vigo, Spain; IRIDIS Group (Investigation in Rheumatology and Immune-Diseases), Galicia Sur Health Research Institute, Vigo, Spain, 22Hospital de Gran Canaria Doctor Negrin, Las Palmas GC, Spain, 23Research Unit, Spanish Society of Rheumatology, Madrid, Spain, Madrid, Spain, 24Department of Rheumatology, Hospital Universitario 12 de Octubre, Madrid, Spain, Madrid, Madrid, Spain, 25Department of Rheumatology, Hospital Gregorio Marañón, Madrid, Spain, Madrid, Madrid, Spain, 26Department of Rheumatology, Hospital Universitario Araba, School of Medicne, Universidad del País Vasco, BIOARABA Health Research Institute, Vitoria, Spain, Vitoria, Pais Vasco, Spain, 27Hospital Regional Universitario de Malaga, Malaga, Spain, Malaga, Spain, 28Department of Rheumatology, Hospital de Jerez, Spain, Puerto De Santa María, Spain, 29Hospital Universitario de la Princesa, Madrid, Spain, 30Hospital Universitario de Bellvitge, Barcelona, Spain, 31Johnson & Johnson, Spring House, PA, USA, Spring House

Meeting: ACR Convergence 2025

Keywords: Biologicals, glucocorticoids, registry, Systemic lupus erythematosus (SLE)

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Session Information

Date: Tuesday, October 28, 2025

Title: (1877–1913) Epidemiology & Public Health Poster III

Session Type: Poster Session C

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

Background/Purpose: The management of SLE varies worldwide. Current SLE treatment goals focus on preventing flares, controlling disease activity, and preventing organ damage accrual. LupusNet is the largest federated data network in SLE that combines and harmonizes data from 5 existing registries to enable greater data consistency and enhance understanding of global clinical presentations and outcomes of SLE. This study assessed treatment patterns for patients with SLE, categorized by disease severity, from LupusNet and a US claims database.

Methods: Data from 3 of 5 SLE registries in LupusNet, APLC (Asia Pacific), RELESSER (Europe), and Almenara (South America), were analyzed from 2012 to 2024, using a privacy-preserving federated data network approach where only aggregated results were shared. Additionally, data from the US Merative MarketScan® Commercial Claims and Encounters (CCAE) Database from 2019 to 2024 were included in the analysis. In LupusNet, data from patients with ≥3 years of follow-up and ≥3 follow-up visits were collected and stratified into mild, moderate, or severe disease based on a SLEDAI score at year 3 follow-up visit (Table 1). In the US claims database, data from patients who were diagnosed with SLE were stratified by mild, moderate, or severe disease based on documented symptoms and clinical features (Table 1). Treatment exposures (ie, glucocorticoids, antimalarials, immunosuppressants, biologic therapies, and other immunosuppressants/immunomodulators) were assessed over follow-up.

Results: LupusNet included 3857 eligible patients: 3070 with mild disease, 637 with moderate disease, and 150 with severe disease. US claims data included 49,350 eligible patients: 23,461 with mild disease, 16,172 with moderate disease, and 9717 with severe disease. Glucocorticoid use was widespread across all disease severity levels: 63%-65% of patients with mild disease, 76%-84% with moderate disease, and 89%-95% with severe disease received glucocorticoids in both LupusNet and US claims data (Figure 1). Antimalarials were also frequently prescribed in 58%-66% of patients, regardless of disease severity. In contrast, use of immunosuppressants varied with disease severity: 25%-50% of patients with mild disease, 43%-67% with moderate disease, and 69%-81% with severe disease received immunosuppressants. Biologic therapies and other immunosuppressants/immunomodulators were utilized less frequently across all disease severity levels in LupusNet (4% and 2%-4%, respectively), while the use of these therapies increased with disease severity in US claims data (8%-44% and 4%-13%, respectively).

Conclusion: This analysis of patient data from LupusNet registries and the US claims database revealed that a considerable number of patients with active, severe SLE across geographic locations were not receiving immunosuppressants or biologic therapies. This suggests a heavy dependence on glucocorticoids to control disease activity and a potential underutilization of steroid-sparing therapies. Additional research is needed to explore long-term treatment trends and barriers to accessing treatments in patients with SLE.

Supporting image 1

Supporting image 2


Disclosures: A. Orillion: Johnson & Johnson, 3, 11; F. Zazzetti: Johnson & Johnson, 3, 11; A. Sheahan: Johnson & Johnson, 3, 12, may hold stock options; C. Blacketer: Johnson & Johnson, 3, 12, may hold stock options; M. van Speybroeck: Johnson & Johnson, 3, 12, may hold stock options; S. Gasman: Johnson & Johnson, 3, 12, may hold stock options; R. Sonmez: Johnson & Johnson, 2, 12, may hold stock options; E. Noss: Johnson & Johnson, 3, 12, may hold stock options; M. Ugarte-Gil: AstraZeneca, 2, 6, Ferrer, 2, 6, GSK, 2, 6, Johnson & Johnson, 5, Novartis, 2, 6, Tecnofarma, 2, 6; R. Gamboa-Cárdenas: None; V. Pimentel-Quiroz: None; K. Michaud: None; P. Katz: None; R. Kandane-Rathnayake: Bristol-Myers Squibb(BMS), 5, GlaxoSmithKline (GSK), 5, Novartis, 5; E. Morand: AbbVie, 2, 5, Amgen, 5, AstraZeneca, 1, 2, 5, 6, Biogen, 1, 2, 5, 6, Bristol Meyers Squibb, 1, 2, 5, 6, Dragonfly, 1, 2, 6, Eli Lilly, 1, 2, 5, 6, EMD Serono, 1, 2, 5, 6, Genentech, 5, GSK, 1, 2, 5, 6, Johnson & Johnson, 5, Novartis, 2, 5, 6, Quell, 1, 2, 6, Remegen, 1, 2, 6, Takeda, 5, UCB, 1, 2, 5, Zenas, 1, 2, 6; W. Louthrenoo: None; A. Hoi: AstraZeneca, 1, 5, 12, contract research, Bristol-Myers Squibb(BMS), 5, Eli Lilly, 5, GlaxoSmithKline (GSK), 1, Johnson & Johnson, 1, Merck/MSD, 12, contract research, UCB, 5; Y. Chen: Abbvie, 12,, 2, 6, Agnitio Science Technology, 2, 6, Astellas, 12,, 2, 6, AstraZeneca, 12,, 2, 6, Biogen, 12,, BMS, 12,, 2, 6, Boehringer-Ingelheim, 12,, Celldex, 12,, CSL Behring, 2, 6, Eisai, 2, 6, Gilead, 12,, 2, 6, GSK, 12,, 2, 6, Guigai, 12,, 2, 6, Inova Diagnostics, 2, 5, Johnson & Johnson, 12,, 2, 6, Lilly, 2, 6, Medigen Vaccine Biologics, 12,, MSD, 12,, 2, 6, Novartis, 2, 6, Pfizer, 12,, 2, 6, Roche, 12,, Sanofi, 12,, 2, 6, Taichung Veterans General Hospital, 12,, Taiwan Department of Health, 12,, Taiwan Ministry of Science and Technology, 12,, Thermo Fisher, 2, 6, UCB, 12,, 2, 6, United Biopharma, 2, 6; J. Cho: None; L. Hamijoyo: None; S. Luo: None; S. Navarra: Astellas, 2, 6, AstraZeneca, 2, 6, Aurinia, 2, 6, Biogen, 2, 12, Independent Data Monitoring Committee, Viatris (Idorsia), 2, 6; M. Nikpour: AstraZeneca, 2, 6, Boehringer-Ingelheim, 2, 6, Bristol-Myers Squibb(BMS), 2, 6, GlaxoSmithKline (GSK), 2, 6, Johnson & Johnson, 2, 6; J. Pego-Reigosa: AstraZeneca, 1, 5, 6, GlaxoSmithKline (GSK), 1, 5, 6, Otsuka, 1, 6; I. Rúa-Figueroa: None; Z. Plaza: None; M. Galindo-Izquierdo: None; J. Martínez Barrio: None; J. Calvo: None; A. Fernández-Nebro: Argenx, 5, AstraZeneca, 2, 5, 6, Chemo, 5, Eli Lilly, 2, 6, Galapagos, 2, 5, 6, Gebro Pharma, 2, 6, GlaxoSmithKline (GSK), 2, 6, Johnson & Johnson, 5, Merck Serono, 5, MSD, 5, Novartis, 2, 5, 6, Takeda, 5, UCB, 5; R. Menor Almagro: None; E. TOMERO MURIEL: None; J. Narváez: None; C. Karyekar: Johnson & Johnson, 12, Former employee and may hold stock options.

To cite this abstract in AMA style:

Orillion A, Zazzetti F, Sheahan A, Blacketer C, van Speybroeck M, Gasman S, Sonmez R, Noss E, Ugarte-Gil M, Gamboa-Cárdenas R, Pimentel-Quiroz V, Michaud K, Katz P, Kandane-Rathnayake R, Morand E, Louthrenoo W, Hoi A, Chen Y, Cho J, Hamijoyo L, Luo S, Navarra S, Nikpour M, Pego-Reigosa J, Rúa-Figueroa I, Plaza Z, Galindo-Izquierdo M, Martínez Barrio J, Calvo J, Fernández-Nebro A, Menor Almagro R, TOMERO MURIEL E, Narváez J, Karyekar C. Customized Therapy for SLE: How Disease Severity Influences the Use of Corticosteroids and Biologics in Patients with SLE in the Lupus Federated Data Network (LupusNet) and a US Claims Database [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/customized-therapy-for-sle-how-disease-severity-influences-the-use-of-corticosteroids-and-biologics-in-patients-with-sle-in-the-lupus-federated-data-network-lupusnet-and-a-us-claims-database/. Accessed .
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