» Articles » PMID: 33488787

The Role of Ixekizumab in Non-radiographic Axial Spondyloarthritis

Overview
Date 2021 Jan 25
PMID 33488787
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Among patients with axial spondyloarthritis (axSpA), non-radiographic axial spondyloarthritis (nr-axSpA) is distinguished from ankylosing spondylitis (AS) by a lack of obvious radiographic changes in the sacroiliac joint. Tumor necrosis factor inhibitor (TNFi) has been used as a highly effective treatment in patients with AS and has shown good efficacy and safety in clinical trials in patients with nr-axSpA. As the pathophysiological mechanism for axSpA has started to become better recognized, various drugs other than TNFi, all of which are related to the interleukin-17 (IL-17) axis, are being evaluated in patients with axSpA. IL-17 inhibitors, such as secukinumab and ixekizumab, are effective drugs for patients with AS. A recent clinical trial reported that ixekizumab, a monoclonal antibody against IL-17A, was also effective in patients with nr-axSpA. In a COAST-X study, ixekizumab was superior to a placebo for improving signs and symptoms in patients with nr-axSpA at weeks 16 and 52. The adverse events were no different from those found in previous ixekizumab studies, and no new safety signals were identified. However, when considering several IL-17 inhibitors, it is necessary to obtain sufficient data to identify the exacerbation of extra-articular manifestation. In terms of effectiveness and safety, ixekizumab may be an appropriate alternative to TNFi in nr-axSpA patients.

Citing Articles

The role of ixekizumab in the treatment of nonradiographic axial spondyloarthritis.

Nam B, Kim T Immunotherapy. 2024; 16(9):569-580.

PMID: 38511247 PMC: 11290369. DOI: 10.2217/imt-2023-0015.


Risk Factors of Ixekizumab-Induced Injection Site Reactions in Patients with Psoriatic Diseases: Report from a Single Medical Center.

Chiu I, Tsai T Biomedicines. 2023; 11(6).

PMID: 37371813 PMC: 10296553. DOI: 10.3390/biomedicines11061718.


Secukinumab in axial spondyloarthritis: a narrative review of clinical evidence.

Braun J, Kiltz U, Buhring B, Baraliakos X Ther Adv Musculoskelet Dis. 2021; 13:1759720X211041854.

PMID: 34471428 PMC: 8404628. DOI: 10.1177/1759720X211041854.


Anti-IL-17 Agents in the Treatment of Axial Spondyloarthritis.

Atzeni F, Carriero A, Boccassini L, DAngelo S Immunotargets Ther. 2021; 10:141-153.

PMID: 33977094 PMC: 8104974. DOI: 10.2147/ITT.S259126.

References
1.
Griffiths C, Reich K, Lebwohl M, van de Kerkhof P, Paul C, Menter A . Comparison of ixekizumab with etanercept or placebo in moderate-to-severe psoriasis (UNCOVER-2 and UNCOVER-3): results from two phase 3 randomised trials. Lancet. 2015; 386(9993):541-51. DOI: 10.1016/S0140-6736(15)60125-8. View

2.
Kim H, Kwon S, Jung K, Kim S, Baek H, Seo M . Safety of Resuming Tumor Necrosis Factor Inhibitors in Ankylosing Spondylitis Patients Concomitant with the Treatment of Active Tuberculosis: A Retrospective Nationwide Registry of the Korean Society of Spondyloarthritis Research. PLoS One. 2016; 11(4):e0153816. PMC: 4839632. DOI: 10.1371/journal.pone.0153816. View

3.
Dougados M, Cheng-Chung Wei J, Landewe R, Sieper J, Baraliakos X, Van den Bosch F . Efficacy and safety of ixekizumab through 52 weeks in two phase 3, randomised, controlled clinical trials in patients with active radiographic axial spondyloarthritis (COAST-V and COAST-W). Ann Rheum Dis. 2019; 79(2):176-185. PMC: 7025731. DOI: 10.1136/annrheumdis-2019-216118. View

4.
Rudwaleit M, Landewe R, van der Heijde D, Listing J, Brandt J, Braun J . The development of Assessment of SpondyloArthritis international Society classification criteria for axial spondyloarthritis (part I): classification of paper patients by expert opinion including uncertainty appraisal. Ann Rheum Dis. 2009; 68(6):770-6. DOI: 10.1136/ard.2009.108217. View

5.
Ruyssen-Witrand A, Perry R, Watkins C, Braileanu G, Kumar G, Kiri S . Efficacy and safety of biologics in psoriatic arthritis: a systematic literature review and network meta-analysis. RMD Open. 2020; 6(1). PMC: 7046955. DOI: 10.1136/rmdopen-2019-001117. View