Clinical response among golimumab-treated Japanese patients with rheumatoid arthritis by number of previous biologic therapies: Real-world evidence from


Journal

Modern rheumatology
ISSN: 1439-7609
Titre abrégé: Mod Rheumatol
Pays: England
ID NLM: 100959226

Informations de publication

Date de publication:
May 2021
Historique:
pubmed: 18 7 2020
medline: 22 6 2021
entrez: 18 7 2020
Statut: ppublish

Résumé

To assess the real-world effectiveness of golimumab in Japanese patients with rheumatoid arthritis who had previously received one or more biologic therapies. A While treatment persistence is comparable, the response to golimumab declined with an increasing number of previous biologic therapies. When stratified by golimumab dose, patients receiving golimumab at 100 mg had higher disease activity at baseline with an increasing number of previous bDMARDs, but they still achieved comparable disease activity at 24 weeks regardless of how many bDMARDs had been previously used. Univariate and multivariate analyses both identified concomitant oral corticosteroid therapy as a factor negatively associated with the likelihood of achieving a DAS28-CRP response. Switching to golimumab was effective regardless of how many biologic agents had been previously used, but the response declined with an increasing number of prior biologic agents. A golimumab dose of 100 mg was also effective for those who previously received three or more bDMARDs.

Identifiants

pubmed: 32678990
doi: 10.1080/14397595.2020.1797283
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antirheumatic Agents 0
Biological Products 0
golimumab 91X1KLU43E

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

566-574

Auteurs

Hirohito Shimizu (H)

Immunology Department, Medical Affairs Division, Janssen Pharmaceutical K.K., Tokyo, Japan.

Hisanori Kobayashi (H)

External Collaboration and Portfolio Management Department, Clinical Science Division, R&D Janssen Pharmaceutical K.K., Tokyo, Japan.

Masayoshi Kanbori (M)

Japan Safety & Surveillance Division, Research & Development Division (R&D), Janssen Pharmaceutical K.K., Tokyo, Japan.

Yutaka Ishii (Y)

Immunology Department, Medical Affairs Division, Janssen Pharmaceutical K.K., Tokyo, Japan.

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Classifications MeSH