TY - JOUR
T1 - Secukinumab efficacy on enthesitis in patients with ankylosing spondylitis
T2 - Pooled analysis of four pivotal phase III studies
AU - Schett, Georg
AU - Baraliakos, Xenofon
AU - van den Bosch, Filip
AU - Deodhar, Atul
AU - Østergaard, Mikkel
AU - Gupta, Ayan Das
AU - Mpofu, Shephard
AU - Fox, Todd
AU - Winseck, Adam
AU - Porter, Brian
AU - Shete, Abhijit
AU - Gensler, Lianne S.
N1 - Publisher Copyright:
© 2021 Journal of Rheumatology. All rights reserved.
PY - 2021/8/1
Y1 - 2021/8/1
N2 - Objective. To assess the efficacy of secukinumab on axial and peripheral enthesitis in patients with ankylosing spondylitis (AS) using pooled data from randomized controlled phase III studies. Methods. In this posthoc analysis, data were pooled from patients originally randomized to secukinumab 150 mg, 300 mg, or placebo (PBO) from phase III MEASURE 1-4 studies (ClinicalTrials.gov: NCT01358175, NCT01649375, NCT02008916, and NCT02159053). Maastricht AS Enthesitis Score (MASES) was used for assessments of enthesitis through Week 52. Efficacy outcomes were mean change in MASES score and complete resolution (MASES = 0) of enthesitis in patients with baseline MASES > 0. Results. A total of 693 (71.5%) patients had enthesitis at baseline in secukinumab 300 mg, 150 mg, and PBO groups (58 [76.3%], 355 [70.4%], and 280 [72%], respectively) out of 969 patients pooled in this analysis. At Week 16, mean changes from baseline for overall MASES and enthesitis at axial MASES sites, respectively, were as follows: -2.9 (P < 0.01) and -2.9 (P < 0.01) for secukinumab 300 mg; -2.4 (P < 0.015) and -2.3 (P< 0.05) for secukinumab 150 mg; and -1.9 and -1.8 for PBO, with improvements seen through Week 52. More than one-third of secukinumab-treated patients (300 mg: 36.2%; 150 mg: 40.8%) achieved complete resolution of enthesitis at Week 16. Conclusion. Secukinumab improved enthesitis at overall MASES and axial sites in patients with AS.
AB - Objective. To assess the efficacy of secukinumab on axial and peripheral enthesitis in patients with ankylosing spondylitis (AS) using pooled data from randomized controlled phase III studies. Methods. In this posthoc analysis, data were pooled from patients originally randomized to secukinumab 150 mg, 300 mg, or placebo (PBO) from phase III MEASURE 1-4 studies (ClinicalTrials.gov: NCT01358175, NCT01649375, NCT02008916, and NCT02159053). Maastricht AS Enthesitis Score (MASES) was used for assessments of enthesitis through Week 52. Efficacy outcomes were mean change in MASES score and complete resolution (MASES = 0) of enthesitis in patients with baseline MASES > 0. Results. A total of 693 (71.5%) patients had enthesitis at baseline in secukinumab 300 mg, 150 mg, and PBO groups (58 [76.3%], 355 [70.4%], and 280 [72%], respectively) out of 969 patients pooled in this analysis. At Week 16, mean changes from baseline for overall MASES and enthesitis at axial MASES sites, respectively, were as follows: -2.9 (P < 0.01) and -2.9 (P < 0.01) for secukinumab 300 mg; -2.4 (P < 0.015) and -2.3 (P< 0.05) for secukinumab 150 mg; and -1.9 and -1.8 for PBO, with improvements seen through Week 52. More than one-third of secukinumab-treated patients (300 mg: 36.2%; 150 mg: 40.8%) achieved complete resolution of enthesitis at Week 16. Conclusion. Secukinumab improved enthesitis at overall MASES and axial sites in patients with AS.
KW - Ankylosing spondylitis
KW - Biological therapy
KW - Inflammation
KW - Interleukin
KW - Spondyloarthropathy
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U2 - 10.3899/jrheum.201111
DO - 10.3899/jrheum.201111
M3 - Article
C2 - 33722947
AN - SCOPUS:85112301680
SN - 0315-162X
VL - 48
SP - 1251
EP - 1258
JO - Journal of Rheumatology
JF - Journal of Rheumatology
IS - 8
ER -