Open AccessAdjunctive methotrexate for treatment of giant cell arteritis: An individual patient data meta‐analysis
Author(s) -
Mahr Alfred D.,
Jover Juan A.,
Spiera Robert F.,
HernándezGarcía César,
FernándezGutiérrez Benjamin,
LaValley Michael P.,
Merkel Peter A.
Publication year - 2007
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.22754
Subject(s) - medicine , placebo , discontinuation , giant cell arteritis , hazard ratio , adverse effect , confidence interval , methotrexate , randomized controlled trial , surgery , gastroenterology , vasculitis , pathology , disease , alternative medicine
Objective To reevaluate the efficacy and safety of adjunctive low‐dose methotrexate (MTX) in giant cell arteritis (GCA). Methods An individual patient data meta‐analysis of 3 randomized placebo‐controlled trials in patients with newly diagnosed GCA was performed. Treatment consisted of initial high‐dose corticosteroids and randomly assigned oral MTX therapy (7.5–15 mg/week) or placebo. Time‐to‐event outcomes were compared between groups using Cox proportional hazards models stratified by trial, and continuous outcomes were compared by calculating weighted mean differences. Results The combined data set comprised 161 patients, of whom 84 received MTX and 77 received placebo. The mean duration of followup was 54.7 weeks (SD 39.2 weeks). Hazard ratios (HRs) for a first and second relapse of GCA were 0.65 ( P = 0.04) and 0.49 ( P = 0.02), respectively, in patients receiving MTX as compared with patients receiving placebo. Accordingly, a predicted 3.6 individuals (95% confidence interval [95% CI] 2.2–56.8) and 4.7 individuals (95% CI 3.3–21.9) need to be treated with MTX to prevent the occurrence of one first or one second relapse, respectively, up to 48 weeks. Use of MTX resulted in a reduction in the corticosteroid cumulative dose by 842 mg within 48 weeks ( P < 0.001). Moreover, MTX treatment was associated with a higher probability of achieving sustained discontinuation of corticosteroids for ≥24 weeks (HR 2.84, P = 0.001). Dropout rates and occurrence of adverse events did not differ between treatment groups. Conclusion In GCA, adjunctive treatment with MTX lowers the risk of relapse and reduces exposure to corticosteroids. These findings indicate that MTX could be considered as a therapeutic option in addition to standard‐of‐care treatment with corticosteroids for patients with GCA.