Effects of concomitant glucocorticoids in TOZURA, a common-framework study programme of subcutaneous tocilizumab in rheumatoid arthritis.
Adult
Aged
Antibodies, Monoclonal, Humanized
/ administration & dosage
Antirheumatic Agents
/ administration & dosage
Arthritis, Rheumatoid
/ drug therapy
Drug Therapy, Combination
Female
Glucocorticoids
/ administration & dosage
Humans
Injections, Subcutaneous
Male
Middle Aged
Prednisone
/ administration & dosage
Treatment Outcome
RA
biologic therapies
csDMARDs
glucocorticoid
tocilizumab
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
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
1056-1064Informations de copyright
© The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Rheumatology.
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