Management of patients with inflammatory rheumatic diseases after treatment failure with a first TNF inhibitor: a narrative review.
Axial spondyloarthritis
TNF-inhibitor failure
juvenile idiopathic arthritis
psoriatic arthritis
rheumatoid arthritis
Journal
Modern rheumatology
ISSN: 1439-7609
Titre abrégé: Mod Rheumatol
Pays: England
ID NLM: 100959226
Informations de publication
Date de publication:
06 Apr 2023
06 Apr 2023
Historique:
received:
21
11
2022
revised:
04
03
2023
accepted:
05
04
2023
entrez:
6
4
2023
pubmed:
7
4
2023
medline:
7
4
2023
Statut:
aheadofprint
Résumé
The emergence of biologics with different modes of action (MoA) and therapeutic targets have changed treatment patterns in patients with inflammatory rheumatic diseases. While tumour necrosis factor inhibitors (TNFi) are often utilized as the first biologic disease-modifying antirheumatic drug, some patients may not respond adequately (primary failure), fail to sustain response over time (secondary failure), or experience intolerable adverse events. Whether these patients would benefit more from cycling to a different TNFi or switching to a biologic with a different MoA is still unclear. We discuss here treatment outcomes of TNFi cycling versus MoA switching after treatment failure with a first TNFi in patients with inflammatory rheumatic diseases, focusing specifically on rheumatoid arthritis, psoriatic arthritis, axial spondyloarthritis, and juvenile idiopathic arthritis. Treatment guidelines for these patients are ambiguous and, at times, contradictory in their recommendations. However, this is due to a lack of high quality head-to-head data to definitively support cycling between TNFi after failure to a first-line TNFi over switching to a different MoA.
Identifiants
pubmed: 37022142
pii: 7109864
doi: 10.1093/mr/road033
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© Japan College of Rheumatology 2023. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.