New advances in the understanding and treatment of axial spondyloarthritis: from chance to choice
- PMID: 29511503
- PMCID: PMC5833172
- DOI: 10.1177/2040622317743486
New advances in the understanding and treatment of axial spondyloarthritis: from chance to choice
Abstract
Axial spondyloarthritis (axSpA) is a chronic inflammatory condition that encompasses ankylosing spondylitis (AS) as well as non-radiographic axial disease (nr-axSpA) and can lead to chronic pain, structural damage and disability. The introduction of tumour necrosis factor inhibitor (TNFi) drugs for AS heralded a new era of drug therapeutics for what was previously a largely untreatable disease. This has now been expanded with the licensing of secukinumab, an interleukin 17A (IL-17A) inhibitor for the treatment of AS. Although biologic disease modifying antirheumatic drugs (bDMARDs) are not a first line treatment option in AS or axSpA, they are highly effective following incomplete or no response to physiotherapy and non-steroidal anti-inflammatory drugs (NSAIDs). Current research strategies aim to test whether the desired treatment goal of disease remission may now be achievable with early and stratified use of bDMARDs in both AS and nr-axSpA. This review summarizes the current literature on axSpA including pathophysiology, treatment indications, radiographic progression and the evidence for new developments in the treatment of both AS and nr-axSpA.
Keywords: IL-17A; JAK inhibitors; SpA; ankylosing spondylitis; anti-TNF; axSpA; axial psoriatic arthritis; biologic therapies; sacroiliitis; secukinumab.
Conflict of interest statement
Conflict of interest statement: The authors declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: The authors Professor Dennis McGonagle and Dr Helena Marzo-Ortega have received grants and/or honoraria from Abbvie, Celgene, Janssen, Elli-Lilly, MSD, Novartis, Pfizer and UCB.
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