TY - JOUR
T1 - Overall and Sex-Specific Predictors of Secukinumab Effectiveness in European Patients With Psoriatic Arthritis
T2 - Results From the EuroSpA Collaboration
AU - Heberg, Jette
AU - Georgiadis, Stylianos
AU - Ahmadzay, Zohra Faizy
AU - Glintborg, Bente
AU - Castrejón, Isabel
AU - Kazemi, Mehrdad Shoae
AU - Loft, Anne Gitte
AU - Michelsen, Brigitte
AU - Rasmussen, Simon Horskjær
AU - Laas, Karin
AU - Vorobjov, Sigrid
AU - Sánchez-Alonso, Fernando
AU - Rotar, Ziga
AU - Pirkmajer, Katja Perdan
AU - Šenolt, Ladislav
AU - Gudbjornsson, Bjorn
AU - Gröndal, Gerdur
AU - Codreanu, Catalin
AU - Iannone, Florenzo
AU - Atzeni, Fabiola
AU - Mann, Heřman
AU - Nordström, Dan
AU - Hokkanen, Anna-Mari
AU - Garcia, Jorge
AU - Barcelos, Filipe
AU - Mielnik, Pawel
AU - Kvien, Tore K.
AU - Kenar-Artin, Gokce
AU - van de Sande, Marleen
AU - Nissen, Michael J.
AU - Müller, Burkhard
AU - Olofsson, Tor
AU - Wallman, Johan K.
AU - Hetland, Merete Lund
AU - Østergaard, Mikkel
AU - Ørnbjerg, Lykke Midtbøll
N1 - Publisher Copyright:
© 2026, The Journal of Rheumatology. This is an Open Access article, which permits use, distribution, and reproduction, without modification, provided the original article is correctly cited and is not used for commercial purposes. All rights reserved.
PY - 2026/9/1
Y1 - 2026/9/1
N2 - Objective. Identifying patient characteristics that predict treatment response in psoriatic arthritis (PsA) may help optimize treat-to-target strategies. We aimed to explore overall and sex-specific predictors of secukinumab (SEC) effectiveness in European patients with PsA treated in routine care. Methods. We analyzed data from 14 registries in the European Spondyloarthritis (EuroSpA) Research Collaboration. Patients aged ≥ 18 years at diagnosis, initiating SEC treatment from January 2015 to January 2021, were included. Multiple imputation was used for missing covariates at treatment start (baseline) and Disease Activity Index for Psoriatic Arthritis based on 28 joints (DAPSA28) at 6 months. Overall and sex-stratified analyses were performed by logistic and Cox regressions to identify baseline predictors of the following treatment outcomes: (1) DAPSA28 low disease activity (LDA; DAPSA28 ≤ 14) at 6 months, (2) DAPSA28 moderate response at 6 months, and (3) SEC discontinuation within 12 months. Results. In total, 2790 patients (43% male) were included. Median age was 43 years (IQR 34-52), and SEC was the first-line biologic/targeted synthetic disease-modifying antirheumatic drug (b/tsDMARD) in 665 patients (24%). Positive predictors for both DAPSA28 LDA and DAPSA28 moderate response were male sex, fewer previous b/tsDMARDs, C-reactive protein (CRP) > 10 mg/L, and lower Health Assessment Questionnaire (HAQ) score. Absence of psoriasis, higher patient fatigue, and tender joint counts predicted SEC discontinuation within 12 months. For some outcomes, sex-specific predictors were fewer previous b/tsDMARDs and CRP > 10 mg/L among male patients and lower patient fatigue score among female patients. Conclusion. We identified overall and sex-specific predictors of SEC effectiveness in European patients with PsA. Our findings may support personalized treatment decisions.
AB - Objective. Identifying patient characteristics that predict treatment response in psoriatic arthritis (PsA) may help optimize treat-to-target strategies. We aimed to explore overall and sex-specific predictors of secukinumab (SEC) effectiveness in European patients with PsA treated in routine care. Methods. We analyzed data from 14 registries in the European Spondyloarthritis (EuroSpA) Research Collaboration. Patients aged ≥ 18 years at diagnosis, initiating SEC treatment from January 2015 to January 2021, were included. Multiple imputation was used for missing covariates at treatment start (baseline) and Disease Activity Index for Psoriatic Arthritis based on 28 joints (DAPSA28) at 6 months. Overall and sex-stratified analyses were performed by logistic and Cox regressions to identify baseline predictors of the following treatment outcomes: (1) DAPSA28 low disease activity (LDA; DAPSA28 ≤ 14) at 6 months, (2) DAPSA28 moderate response at 6 months, and (3) SEC discontinuation within 12 months. Results. In total, 2790 patients (43% male) were included. Median age was 43 years (IQR 34-52), and SEC was the first-line biologic/targeted synthetic disease-modifying antirheumatic drug (b/tsDMARD) in 665 patients (24%). Positive predictors for both DAPSA28 LDA and DAPSA28 moderate response were male sex, fewer previous b/tsDMARDs, C-reactive protein (CRP) > 10 mg/L, and lower Health Assessment Questionnaire (HAQ) score. Absence of psoriasis, higher patient fatigue, and tender joint counts predicted SEC discontinuation within 12 months. For some outcomes, sex-specific predictors were fewer previous b/tsDMARDs and CRP > 10 mg/L among male patients and lower patient fatigue score among female patients. Conclusion. We identified overall and sex-specific predictors of SEC effectiveness in European patients with PsA. Our findings may support personalized treatment decisions.
KW - interleukin 17A inhibitors
KW - psoriatic arthritis
KW - rheumatology
KW - sex
KW - spondyloarthritis
KW - treat-to-target
UR - https://www.scopus.com/pages/publications/105049010851
U2 - 10.3899/jrheum.2025-1023
DO - 10.3899/jrheum.2025-1023
M3 - Journal article
C2 - 42297436
AN - SCOPUS:105049010851
SN - 0315-162X
VL - 53
SP - 977
EP - 985
JO - Journal of Rheumatology
JF - Journal of Rheumatology
IS - 9
ER -