Abstract

BackgroundTo investigate whether the reason to discontinue the first TNF inhibitor (TNFi) affects the response to the second TNFi in axial spondyloarthritis (axSpA).MethodsPatients with axSpA from the Rheumatic Diseases Portuguese Register (ReumaPt), who discontinued their first TNFi and started the second TNFi between June 2008 and May 2018, were included. Response was assessed by the Ankylosing Spondylitis Disease Activity Score (ASDAS) clinically important improvement (ASDAS-CII), major important improvement (ASDAS-MI), low disease activity (ASDAS-LDA), and inactive disease (ASDAS-ID). The reason for discontinuation of the first TNFi was defined, according to ASDAS-CII as primary failure (no response ≤ 6 months), secondary failure (response ≤ 6 months but lost thereafter), adverse events, and others. The association between the reason for discontinuation of the first TNFi and response to the second TNFi over time was assessed in multivariable generalized equation (GEE) models.ResultsIn total, 193 patients were included. The reason for discontinuation of the first TNFi did not influence the response to the second TNFi, according to the ASDAS-CII. However, a difference was found with more stringent outcomes, e.g., there was a higher likelihood to achieve ASDAS-ID with the second TNFi for patients discontinuing the first TNFi due to secondary failure (OR 7.3 [95%CI 1.9; 27.7]), adverse events (OR 9.1 [2.5; 33.3]), or other reasons (OR 7.7 [1.6; 37.9]) compared to primary failure.ConclusionPatients with axSpA with secondary failure to their first TNFi, compared to those with primary failure, have a better response to the second TNFi according to stringent outcomes.

Highlights

  • To investigate whether the reason to discontinue the first TNF inhibitor (TNFi) affects the response to the second TNFi in axial spondyloarthritis

  • TNFi were the only biological diseasemodifying drugs with proved efficacy in axSpA. Secukinumab and ixekizumab, both IL-17 inhibitors (IL-17i), have demonstrated efficacy in phase 3 randomized controlled trials (RCTs) [3,4,5], both in TNFi-naive and TNFi-experienced patients with radiographic axial spondyloarthritis (r-axSpA). Part of these data already translated into a change in the 2016 update of the Assessment of SpondyloArthritis International Society– European League Against Rheumatism (ASAS-EULAR) management recommendations for axSpA [6] which prescribes switching to another TNFi or an IL-17i in case of failure of the first TNFi

  • Patient characteristics In total, 346 patients with axSpA registered in Reuma.pt by the time of database lock (May 2018) had discontinued the first TNFi and started the second TNFi; out of these, 193 had available data for Ankylosing Spondylitis Disease Activity Score (ASDAS) at baseline, 3 and 6 months for the first TNFi, and were included

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Summary

Introduction

To investigate whether the reason to discontinue the first TNF inhibitor (TNFi) affects the response to the second TNFi in axial spondyloarthritis (axSpA). Secukinumab and ixekizumab, both IL-17 inhibitors (IL-17i), have demonstrated efficacy in phase 3 randomized controlled trials (RCTs) [3,4,5], both in TNFi-naive and TNFi-experienced patients with radiographic axial spondyloarthritis (r-axSpA). Part of these data already translated into a change in the 2016 update of the Assessment of SpondyloArthritis International Society– European League Against Rheumatism (ASAS-EULAR) management recommendations for axSpA [6] which prescribes switching to another TNFi or an IL-17i in case of failure of the first TNFi

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