Effects of concomitant glucocorticoids in TOZURA, a common-framework study programme of subcutaneous tocilizumab in rheumatoid arthritis.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
01 06 2019
Historique:
received: 10 09 2018
revised: 01 11 2018
pubmed: 17 1 2019
medline: 23 2 2020
entrez: 17 1 2019
Statut: ppublish

Résumé

This post hoc analysis of the TOZURA study programme evaluated the efficacy and safety of subcutaneous tocilizumab (TCZ-SC) as monotherapy or with concomitant conventional synthetic DMARDs (csDMARDs) in patients with RA categorized by baseline glucocorticoid (GC) use. TOZURA was a multinational, open-label, single-arm, common-framework study programme (11 protocols, 22 countries) in patients with moderate to severe RA in whom csDMARDs or biologic therapies had failed or who were MTX naïve. Patients received once-weekly TCZ-SC 162 mg for ⩾24 weeks as monotherapy or in combination with csDMARDs and/or oral GC use (⩽10 mg/day prednisone or equivalent), which was to be continued unchanged for 24 weeks. Treatment subgroups were defined by baseline GC use and analysed for efficacy and safety. Of 1804 patients who received TCZ-SC, 145 received monotherapy + GC, 208 received monotherapy without GC, 730 received combination therapy + GC and 721 received combination therapy without GC. The median GC dose in both GC subgroups was 5 mg/day. The proportion of patients who achieved clinical remission, defined as DAS in 28 joints using ESR <2.6, increased similarly from baseline to week 24 in all subgroups. Improvements in patient-reported outcomes were similar in all subgroups. Overall adverse event profiles were generally similar between subgroups, with some slight numerical differences between GC and non-GC subgroups. The incremental efficacy benefits of TCZ-SC as monotherapy and in combination with csDMARDs were similar between patients with and without previous and continued oral GC treatment, with generally similar safety profiles. ClinicalTrials.gov, http://www.clinicaltrials.gov, NCT01941940, NCT01941095, NCT01951170, NCT01987479, NCT01988012, NCT01995201, NCT02001987, NCT02011334, NCT02031471, NCT02046603, NCT02046616.

Identifiants

pubmed: 30649524
pii: 5288155
doi: 10.1093/rheumatology/key393
pmc: PMC6532446
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antirheumatic Agents 0
Glucocorticoids 0
tocilizumab I031V2H011
Prednisone VB0R961HZT

Banques de données

ClinicalTrials.gov
['NCT01941095', 'NCT02001987', 'NCT01987479', 'NCT01941940', 'NCT02046616', 'NCT02031471', 'NCT01951170', 'NCT02011334', 'NCT01988012', 'NCT01995201', 'NCT02046603']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1056-1064

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Rheumatology.

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Auteurs

Ernest Choy (E)

Division of Infection and Immunity, CREATE Centre, Cardiff University, Cardiff, UK.

Roberto Caporali (R)

Division of Rheumatology, University of Pavia and Fondazione IRCCS Policlinico S. Matteo Foundation, Pavia, Italy.

Ricardo Xavier (R)

Department of Medicine, Universidade Federal do Rio Grande do Sul Porto Alegre, Rio Grande do Sul, Brazil.

Bruno Fautrel (B)

Department of Rheumatology, AP-HP, Pitié-Salpêtrière Hospital, Pierre and Marie Curie University, Paris, France.

Raimon Sanmarti (R)

Department of Rheumatology, Hospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain.

Min Bao (M)

Genentech, Inc., South San Francisco, CA, USA.

Jenny Devenport (J)

Genentech, Inc., South San Francisco, CA, USA.

Attila Pethö-Schramm (A)

F. Hoffmann-La Roche Ltd, Basel, Switzerland.

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Classifications MeSH