SAT0401 Two-Years Survival of Golimumab in 400 Patients with Rheumatoid Arthritis, Psoriatic Arthritis, and Axial Spondyloarthritis in Real-Life World
BackgroundIt has previously been shown that the survival of anti-TNF drugs was lower in Rheumatoid arthritis (RA) than in other chronic arthritis.ObjectivesThe objective of this study was to investigate the drug retention, as surrogate of effectiveness, of Golimumab (GOL) with axial Spondyloarthriti...
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Veröffentlicht in: | Annals of the rheumatic diseases 2016-06, Vol.75 (Suppl 2), p.814-815 |
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Zusammenfassung: | BackgroundIt has previously been shown that the survival of anti-TNF drugs was lower in Rheumatoid arthritis (RA) than in other chronic arthritis.ObjectivesThe objective of this study was to investigate the drug retention, as surrogate of effectiveness, of Golimumab (GOL) with axial Spondyloarthritis (AxSpA), Psoriatic arthritis (PsA) and RA. Furthermore, predictors of drug retention were evaluated.MethodsThis is a multicenter prospective observational study of unselected patients with AxSpA, PsA and RA starting GOL because of their active disease despite prior treatment with conventional disease modifying drugs (DMARDs) or biological DMARDs (bDMARDs) in the settings of standard care from 11 rheumatologic centres of Apulia (Southern Italy). The primary endpoint was GOL drug retention at 2 years. Time to discontinuation was defined as the time between drug initiation and last administration plus one dispensation interval. Kaplan-Meier curve analysis was used to assess drug retention, and a Cox proportional regression model, adjusting for potential confounders, including prior bDMARD exposure, glucocorticoid or DMARD intake, patient demographics and disease characteristics, for the analysis of predictors. Clinical response was evaluated at 3,6,12 and 24 months.ResultsTo date, 416 patients (PsA 180, RA 89, AxSpA 147) have been included in the study, 171 (41%) were biologic-naïve. Disease duration was 6.9 ±6 yrs for PsA, 8.1 ±8 for RA, and 7.4 ±7 for AxSpA, respectively. RF/ACPA were present in 72.5% of RA patients, and HLA-B27 in 43% of AxSpa. Within PsA 58 patients had also spinal involvement. At 2 years (Fig.1), the drug persistence rate was 74.5% (20.8±0.5 months) for AxSpa, 62.5% (19.5±0.8 months) for RA, and 63.9% (18.8±0.6) months for PsA, being the difference not statistically significant. For AxSpa patients, the chance of stopping GOL was associated with the female gender (hazard ratio (HR) 3.15 (95% CI 1.4–8.5), and the presence of extra-articular manifestation (HR 0.20 (95% CI 0.48–0.88). In RA the only predictor of GOL discontinuation was the achievement good EULAR response at 3 months (HR 0.36 ((95% CI 0.15–0.88), while no baseline factors correlating with drug persistence was detected for PsA. The percentage of AxSpa patients achieving BASDAI |
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ISSN: | 0003-4967 1468-2060 |
DOI: | 10.1136/annrheumdis-2016-eular.2475 |