Objective Inflammation at the entheses is a distinguishing feature of spondyloarthritis (SpA). Enthesitis at the heel is the most common location and is often chronic, refractory to standard treatment and may have socioeconomic consequences. The objective of this study was to investigate the efficacy of etanercept in refractory heel enthesitis related to SpA.
Methods The present work was a 12-week, randomised, double-blind, placebo-controlled study compared etanercept with placebo in patients with SpA according to Amor's criteria, and heel enthesitis proven by MRI. The primary efficacy end point was the normalised net incremental area under the curve (AUC) between randomisation and week 12 for the patient's global assessment (PGA) of disease activity. Secondary end points included change from baseline in PGA, heel pain, the Western Ontario and McMaster Universities Osteoarthritis index (WOMAC) function subscale and improvement in enthesitis as measured by MRI.
Results A total of 24 patients were randomised. Mean normalised net incremental AUC for PGA of disease activity over 12 weeks was significantly greater in the etanercept versus placebo group: −28.5 versus −11.1, respectively (p=0.029). Significant improvements were also reported in the etanercept versus placebo group for PGA, −37.6 versus −11.6 (p=0.007); heel pain, −36.7 versus −13.1 (p=0.022); and WOMAC function, −23.2 versus −7.8 (p=0.024). No significant changes were observed in the MRI findings between groups. No unexpected adverse events or changes in laboratory values or vital signs.
Conclusions This trial is the first randomised placebo-controlled study of an anti-tumour necrosis factor (TNF) agent in refractory heel enthesitis in patients with SpA. It demonstrates that etanercept has a statistically significant and clinically relevant benefit in such patients.
ClinicalTrials.gov identifier NCT00420303.
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Funding This study was sponsored by Wyeth Pharmaceuticals.
Competing interests MD, Wyeth Pharmaceuticals, consulting fees or other remuneration. BC, Schering, UCB, Wyeth Pharmaceuticals, research grants; UCB, Schering, Wyeth Pharmaceuticals: consulting fees or other remuneration. JB, Wyeth Pharmaceuticals, consulting fees or other remuneration. RL, Wyeth Pharmaceuticals, consulting fees or other remuneration. JS, Bristol-Myers Squibb, Roche Pharmaceuticals, Schering-Plough, research grants; Abbott Immunology Pharmaceuticals, Actelion, Bristol-Myers Squibb, GlaxoSmithKline, LFB, Merck Sharp Dohme, Pfizer Inc, Roche Pharmaceuticals, Schering-Plough, UCB, Wyeth Pharmaceuticals, consulting fees or other remuneration. AC, Roche Pharmaceuticals, research grants; Abbott Immunology Pharmaceuticals, Bristol-Myers Squibb, Merck Pharmaceuticals, Wyeth Pharmaceuticals, consulting fees or other remuneration. DvdH, Abbott, Amgen, Aventis, Bristol-Myers Squibb, Centocor, Pfizer, Roche, Schering-Plough, UCB, Wyeth Pharmaceuticals consulting fees or other remuneration. VL, Wyeth Pharmaceuticals, employment. IL, Wyeth Pharmaceuticals, employment.
Ethics approval This study was conducted with the approval of the ERC Cochin Hospital, Paris, France.
Provenance and peer review Not commissioned; externally peer reviewed.