Factors associated with the retention of secukinumab in patients with axial spondyloarthritis in real-world practice: results from a retrospective study (FORSYA).
Maxime DougadosJulien LucasEmilie DesfleursPascal ClaudepierrePhilippe GoupilleAdeline Ruyssen-WitrandAlain SarauxAnne TournadreDaniel WendlingCédric LukasPublished in: RMD open (2023)
Following its approval in France, ~59% of axSpA patients retained secukinumab in daily practice, at 1 year. Prior exposure to TNFi, OSI and IBD were identified as risk factors for secukinumab discontinuation.