Biologic therapy and spinal radiographic progression in patients with axial spondyloarthritis: A structured literature review.
ankylosing spondylitis
biologic therapy
interleukin-17A inhibitor
radiography
tumor necrosis factor inhibitor
Journal
Therapeutic advances in musculoskeletal disease
ISSN: 1759-720X
Titre abrégé: Ther Adv Musculoskelet Dis
Pays: England
ID NLM: 101517322
Informations de publication
Date de publication:
2020
2020
Historique:
received:
04
10
2019
accepted:
09
01
2020
entrez:
18
3
2020
pubmed:
18
3
2020
medline:
18
3
2020
Statut:
epublish
Résumé
We aimed to perform a structured literature review of spinal radiographic progression, as assessed by the modified Stoke Ankylosing Spondylitis Spine Score (mSASSS), in patients with ankylosing spondylitis (AS) or nonradiographic axial spondyloarthritis (nr-axSpA) treated with biologic therapy. Searches were limited to English language manuscripts published in the 11 years prior to 9 July 2019. Randomized controlled trials, open-label extensions (OLEs) and observational studies reporting mSASSS progression in patients with AS or nr-axSpA treated with biologics were eligible for inclusion. Bias was assessed using the methodological index for nonrandomized studies (MINORS) tool. Among the 322 studies identified in the literature search, 23 (11 OLEs and 12 cohort studies) met the eligibility criteria and were selected for inclusion. Most studies reported mSASSS progression in patients with AS receiving tumor necrosis factor inhibitor (TNFi) treatment. One study reported mSASSS progression in patients with AS treated with secukinumab, an interleukin-17A inhibitor. The mean (range) MINORS score was 11.3 (7-15) for the 15 noncomparative studies and 15 (12-22) for the 8 comparative studies. Although results of the individual studies were variable, mSASSS progression in patients with AS was generally minimal and slow with long-term TNFi therapy. Moreover, odds ratios for the likelihood of mSASSS progression with/without TNFi favoured TNFi therapy in several of the cohort studies. The rate of mSASSS progression following continuous secukinumab treatment was low and remained stable over 4 years. Of two studies reporting progression in patients with nr-axSpA treated with TNFis, one showed no mSASSS progression; however, the lack of control limited comparative conclusions.
Identifiants
pubmed: 32180840
doi: 10.1177/1759720X20906040
pii: 10.1177_1759720X20906040
pmc: PMC7057409
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
1759720X20906040Informations de copyright
© The Author(s), 2020.
Déclaration de conflit d'intérêts
Conflict of interest statement: Xenofon Baraliakos reports consultancy or speaker’s fees from AbbVie, BMS, Celgene, Chugai, Hexal, Galapagos, Janssen, Lilly, MSD, Novartis, Pfizer, Sandoz, Sanofi and UCB Pharma. Lianne S. Gensler reports grants from AbbVie, Amgen, Novartis, Pfizer and UCB Pharma, and personal fees from Galapagos, Janssen, Lilly, Novartis, Pfizer and UCB Pharma. Salvatore D’Angelo reports consultancy fees from AbbVie, BMS, Janssen, MSD, Novartis, Pfizer and UCB Pharma. Florenzo Iannone reports consultancy or speaker’s fees from AbbVie, BMS, Celgene, Janssen, MSD, Novartis, Pfizer and Roche. Ennio G. Favalli reports consultancy and lecture fees from AbbVie, MSD, Novartis, Pfizer and UCB Pharma. Natasha de Peyrecave and Simone E. Auteri are employees of UCB Pharma. Roberto Caporali reports speaker’s fees from AbbVie, BMS, Celgene, HSD, Lilly, Pfizer, Roche and UCB Pharma.
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