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Short-term prednisolone bridging enables 95% discontinuation in new rheumatoid arthritis patients after 24 months

Short-term prednisolone bridging enables 95% discontinuation in new rheumatoid arthritis patients…
Photo by HI! ESTUDIO / Unsplash
Key Takeaway
Consider short-term prednisolone bridging to enable methotrexate monotherapy in new rheumatoid arthritis patients.

This randomized controlled trial included 230 patients with newly diagnosed rheumatoid arthritis who were naive to disease-modifying antirheumatic drugs. The intervention involved short-term bridging therapy with prednisolone using tapering doses from 15 mg to 0 over 7 weeks, followed by methotrexate monotherapy. The comparator was not reported in the provided data.

The primary outcome measured the proportion of patients successfully discontinuing prednisolone. At 7 weeks, 84% of patients discontinued the drug, representing 191 out of 227 individuals. By 3 months, this proportion rose to 89%, or 203 out of 227 patients. At the 24-month follow-up, 95% of patients had discontinued prednisolone, corresponding to 216 out of 227 individuals.

Regarding secondary outcomes, 5% of patients, or 11 out of 227, required continuous use of prednisolone at every visit. Among those who discontinued after 7 weeks, 80% did not restart the medication, which equates to 152 out of 191 patients. Continuous use for at least 3 months occurred in 22% of the cohort. Safety data, including adverse events and tolerability, were not reported. Discontinuations due to adverse events were not reported.

The study supports the conclusion that tapering to discontinuation is achievable in most patients after short-term bridging with prednisolone. This finding aligns with current European Alliance of Associations for Rheumatology recommendations. The study phase was not reported, and funding or conflicts of interest were not reported.

Study Details

Study typeRct
Sample sizen = 230
EvidenceLevel 2
Follow-up24.0 mo
PublishedJun 2026
View Original Abstract ↓
OBJECTIVES: The objective of this paper is to examine whether patients with newly diagnosed rheumatoid arthritis (RA) can discontinue prednisolone after short-term bridging therapy. METHODS: Patients naïve to disease-modifying antirheumatic drugs with recent-onset RA in the ARCTIC (Aiming for Remission in rheumatoid arthritis: a randomised trial examining the benefit of ultrasound in a Clinical TIght Control regimen) trial were followed for 24 months, with initial methotrexate monotherapy and prednisolone bridging therapy (tapering doses from 15 mg to 0 over 7 weeks). We explored the proportion of patients successfully discontinuing prednisolone, defined as no prednisolone use after bridging therapy, and for at least 4 subsequent months. Discontinuation was assessed after cessation of bridging therapy at 2, 3, 6, 12, 20, and 24 months. Additionally, we examined how many patients used prednisolone continuously for ≥3 months. RESULTS: Of 230 patients, 227 started prednisolone bridging therapy and were included for analyses. At baseline, mean (SD) age was 52 (13.7) years, mean (SD) disease activity score was 3.47 (1.17), 62% patients were female, and 82% patients were anticitrullinated peptide antibody positive. After 7 weeks, 84% (191/227) had discontinued prednisolone, 89% (203/227) had discontinued at 3 months, and 95% (216/227) within 24 months. Five percent (11/227) used prednisolone at every visit. The median number of days (IQR) of prednisolone use during 2 years was 55 (48-90). Among those who discontinued after 7 weeks, 80% (152/191) did not restart prednisolone. Continuous use for at least 3 months was observed in 22%. CONCLUSIONS: In newly diagnosed patients with RA using bridging therapy when starting methotrexate, over 80% successfully discontinued prednisolone. This supports that tapering to discontinuation is achievable in most patients after short-term bridging with prednisolone, in line with current European Alliance of Associations for Rheumatology recommendations.
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