Predictors of response to secukinumab in patients with psoriatic arthritis and axial manifestations: a post-hoc analysis of the MAXIMISE trial

<strong>Objectives</strong> To investigate patient characteristics predictive of response to secukinumab in patients with psoriatic arthritis (PsA) with axial manifestations. <br><strong> Methods</strong> In a post-hoc analysis from the MAXIMISE trial (NCT02721966) in p...

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Main Authors: Baraliakos, X, Pournara, E, Gossec, L, Mease, P, White, R, O’Brien, E, Schulz, B, Marzo Ortega, H, Coates, LC
Format: Journal article
Language:English
Published: BMJ Publishing Group 2022
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author Baraliakos, X
Pournara, E
Gossec, L
Mease, P
White, R
O’Brien, E
Schulz, B
Marzo Ortega, H
Coates, LC
author_facet Baraliakos, X
Pournara, E
Gossec, L
Mease, P
White, R
O’Brien, E
Schulz, B
Marzo Ortega, H
Coates, LC
author_sort Baraliakos, X
collection OXFORD
description <strong>Objectives</strong> To investigate patient characteristics predictive of response to secukinumab in patients with psoriatic arthritis (PsA) with axial manifestations. <br><strong> Methods</strong> In a post-hoc analysis from the MAXIMISE trial (NCT02721966) in patients with PsA and axial manifestations, we tested the hypothesis that the OR of the effect of treatment on the primary endpoint of the trial (Assessment of SpondyloArthritis international Society (ASAS) 20 responder status at week 12) would be different depending on 12 prespecified predictor variables. We applied a two-model logistic regression approach, a main effects and an interaction model. <br><strong> Results </strong>The OR (95% CI) for ASAS20 response for the presence of nail dystrophy was 3.2 (95% CI 0.93 to 10.99) in the secukinumab 150 mg group and 5.0 (95% CI 1.47 to 17.19) in the secukinumab 300 mg group compared with the placebo group (p=0.029). Odds of being a responder were similar in men and women in the secukinumab groups, though men fared worse than women in the placebo group (p=0.039). Current smokers were less likely to be ASAS20 responders compared with never smokers regardless of the treatment group (p=0.589). <br><strong> Conclusion </strong>Nail dystrophy was identified as a predictor of response to secukinumab in patients with PsA with axial manifestations in the MAXIMISE trial. These findings may be explained by the nail-entheseal concept as part of the axial phenotype in PsA .
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spelling oxford-uuid:99ce4a31-f5d4-44b1-8665-0f6a2252a23f2022-09-28T11:00:31ZPredictors of response to secukinumab in patients with psoriatic arthritis and axial manifestations: a post-hoc analysis of the MAXIMISE trialJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:99ce4a31-f5d4-44b1-8665-0f6a2252a23fEnglishSymplectic ElementsBMJ Publishing Group2022Baraliakos, XPournara, EGossec, LMease, PWhite, RO’Brien, ESchulz, BMarzo Ortega, HCoates, LC<strong>Objectives</strong> To investigate patient characteristics predictive of response to secukinumab in patients with psoriatic arthritis (PsA) with axial manifestations. <br><strong> Methods</strong> In a post-hoc analysis from the MAXIMISE trial (NCT02721966) in patients with PsA and axial manifestations, we tested the hypothesis that the OR of the effect of treatment on the primary endpoint of the trial (Assessment of SpondyloArthritis international Society (ASAS) 20 responder status at week 12) would be different depending on 12 prespecified predictor variables. We applied a two-model logistic regression approach, a main effects and an interaction model. <br><strong> Results </strong>The OR (95% CI) for ASAS20 response for the presence of nail dystrophy was 3.2 (95% CI 0.93 to 10.99) in the secukinumab 150 mg group and 5.0 (95% CI 1.47 to 17.19) in the secukinumab 300 mg group compared with the placebo group (p=0.029). Odds of being a responder were similar in men and women in the secukinumab groups, though men fared worse than women in the placebo group (p=0.039). Current smokers were less likely to be ASAS20 responders compared with never smokers regardless of the treatment group (p=0.589). <br><strong> Conclusion </strong>Nail dystrophy was identified as a predictor of response to secukinumab in patients with PsA with axial manifestations in the MAXIMISE trial. These findings may be explained by the nail-entheseal concept as part of the axial phenotype in PsA .
spellingShingle Baraliakos, X
Pournara, E
Gossec, L
Mease, P
White, R
O’Brien, E
Schulz, B
Marzo Ortega, H
Coates, LC
Predictors of response to secukinumab in patients with psoriatic arthritis and axial manifestations: a post-hoc analysis of the MAXIMISE trial
title Predictors of response to secukinumab in patients with psoriatic arthritis and axial manifestations: a post-hoc analysis of the MAXIMISE trial
title_full Predictors of response to secukinumab in patients with psoriatic arthritis and axial manifestations: a post-hoc analysis of the MAXIMISE trial
title_fullStr Predictors of response to secukinumab in patients with psoriatic arthritis and axial manifestations: a post-hoc analysis of the MAXIMISE trial
title_full_unstemmed Predictors of response to secukinumab in patients with psoriatic arthritis and axial manifestations: a post-hoc analysis of the MAXIMISE trial
title_short Predictors of response to secukinumab in patients with psoriatic arthritis and axial manifestations: a post-hoc analysis of the MAXIMISE trial
title_sort predictors of response to secukinumab in patients with psoriatic arthritis and axial manifestations a post hoc analysis of the maximise trial
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