Arthritis Research & Therapy
Frederik Kreiner (frederik.kreiner@me.com) Henrik Galbo (hga@sund.ku.dk)
Abstract
Introduction: To elucidate in polymyalgia rheumatica (PMR) the role of tumor necrosis factor (TNF) α and the therapeutic potential of blockade with soluble TNF-α receptor, we carried out the first randomized controlled trial with etanercept in PMR.
Methods: Twenty newly diagnosed, glucocorticoid (GC) naïve patients with PMR and 20 matched non-PMR control subjects completed the trial. Subjects were randomized in a 1:1 ratio to monotherapy with etanercept (25 mg s.c. biweekly) or placebo (saline) for 14 days. Study outcomes were assessed at baseline and after 14 days. The primary outcome was the change in PMR activity score (PMR-AS). Secondary outcomes were: changes in erythrocyte sedimentation rate (ESR) and plasma levels of TNF-α and interleukin (IL) 6; patients’ functional status (health assessment questionnaire) and cumulative tramadol intake during the trial.
Results: At baseline, plasma TNF-α was higher in patients than in controls (P<0.05). The concentration always increased with etanercept treatment (P<0.05). In patients, etanercept decreased PMR-AS by 24% (P=0.011), reflecting significant improvements in shoulder mobility, physician’s global assessment and C-reactive protein, and insignificant (P>0.05) improvements in duration of morning stiffness and patient’s assessment of pain. In parallel, ESR and IL-6 were reduced (P<0.05). Placebo treatment did not change PMR-AS, ESR and IL-6 (p>0.05). Functional status did not change and tramadol intake did not differ between patient groups. In controls, no changes occurred in both groups.