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juvenile rheumatoid arthritis;etanercept therapy Article Summary

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Safety and efficacy of up to eight years of continuous etanercept therapy in patients with juvenile rheumatoid arthritis
Arthritis & Rheumatism, 05/16/08
Print     Email This Article     Save in My Library   Free Abstract
Lovell DJ et al. – The acceptable safety profile of etanercept therapy was maintained for up to 8 years in this population of juvenile rheumatoid arthritis (JRA) patients. Improvements in the signs and symptoms of JRA were also maintained for up to 8 years.

Methods
  • Study to evaluate the safety and efficacy of up to 8 yrs of etanercept treatment in pts with polyarticular-course JRA
  • Pts with JRA who previously participated in a randomized controlled trial (RCT) of etanercept were eligible to receive etanercept in a long-term open-label extension (OLE) trial
  • Safety end points included the incidences of serious SAEs, medically important infections (MIIs), and death /li>
  • Efficacy end points included the ACR Pediatric 30 (Pedi 30), Pedi 50, Pedi 70, Pedi 90, and Pedi 100 criteria for improvement

Results
  • 84% of the RCT pts participated in the OLE, for a total of 318 patient-yrs of etanercept exposure
  • 72% of pts entered the fourth year of continuous etanercept treatment, and 45% entered the eighth year
  • 23% of those entering the RCT reported 39 SAEs
  • The overall rate of SAEs did not increase with long-term exposure to etanercept
  • The rate of MIIs remained low; 1 new MII was reported in pts with >=5 yrs of etanercept exposure
  • No cases of tuberculosis, opportunistic infections, malignancies, lymphomas, lupus, demyelinating disorders, or deaths were reported
  • An ACR Pedi 70 response or higher was achieved by 100% of pts with 8 yrs of data and by 61% of pts according to the last observation carried forward data

 

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