Effectiveness of secukinumab in radiographic and non-radiographic axial spondyloarthritis: a European routine-care observational study
Christiansen, Sara Nysom; Rasmussen, Simon Horskjær; Ostergaard, Mikkel; Pons, Marion; Michelsen, Brigitte; Pavelka, Karel; Codreanu, Catalin; Ciurea, Adrian; Glintborg, Bente; Santos, Maria Jose; Sari, Ismail; Rotar, Ziga; Gudbjornsson, Bjorn; Macfarlane, Gary J.; Relas, Heikki; Iannone, Florenzo; Laas, Karin; Wallman, Johan K.; van de Sande, Marleen; Provan, Sella Aarrestad; Castrejon, Isabel; Zavada, Jakub; Mogosan, Corina; Nissen, Michael J.; Loft, Anne Gitte; Barcelos, Anabela; Erez, Yesim; Pirkmajer, Katja Perdan; Grondal, Gerdur; Jones, Gareth T.; Hokkanen, Anna-Mari; Chimenti, Maria Sole; Vorobjov, Sigrid; Giuseppe, Daniela Di; Kvien, Tore Kristian Aaserud; Otero-Varela, Lucia; van der Horst-Bruinsma, Irene; Hetland, Merete Lund; Ørnbjerg, Lykke Midtbøll
Peer reviewed, Journal article
Published version
Date
2024Metadata
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Abstract
Objectives To compare the treatment effectiveness of secukinumab in radiographic (r) versus non-radiographic (nr) axial spondyloarthritis (axSpA) patients treated in routine care across Europe.
Methods Prospectively collected data on secukinumab-treated axSpA patients with known radiographic status were pooled from nine countries.
Remission rates based on patient-reported outcomes (PROs; Numeric Rating Scale (0–10), for example, pain ≤2/Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) ≤2 and Ankylosing Spondylitis Disease Activity Score (ASDAS) inactive disease (ID) <1.3 after 6/12/24 months of secukinumab treatment were calculated.
Remission and drug retention rates in r-axSpA versus nr-axSpA patients were compared by logistic and Cox regression models (unadjusted/adjusted for age+sex/adjusted for multiple confounders).
Results Overall, 1161 secukinumab-treated patients were included (r-axSpA/nr-axSpA: 922/239). At baseline, r-axSpA patients had longer disease duration and higher C reactive protein, were more often male and HLA-B27 positive and had received fewer prior biological or targeted synthetic disease-modifying antirheumatic drugs compared with nr-axSpA patients, whereas PROs were largely similar.
During follow-up, crude PRO remission rates were significantly higher in r-axSpA compared with nr-axSpA patients (6 months: pain≤2: 40%/28%, OR=1.7; BASDAI≤2: 37%/25%, OR=1.8), as were drug retention rates (24 months: 66%/58%, HR 0.73 (ref: r-axSpA)). Proportions of patients achieving ASDAS ID were low for both groups, particularly nr-axSpA (6 months: 11%/8%).
However, when adjusting for age+sex, these differences diminished, and after adjusting for multiple confounders, no significant between-group differences remained for either remission or drug retention rates.
Conclusion Crude remission/drug retention rates in European secukinumab-treated patients were higher in r-axSpA compared with nr-axSpA patients. In adjusted analyses, secukinumab effectiveness was similar in both groups, suggesting that observed differences were related to factors other than radiographic status.