An Analysis of Real-World Data on the Safety of Etanercept in Older Patients with Rheumatoid Arthritis

Christopher J Edwards1, Jack F Bukowski2, Sara M Burns3

  • 1Rheumatology Department, NIHR Clinical Research Facility, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK. cedwards@soton.ac.uk.

Drugs & Aging
|November 13, 2019
PubMed
Abstract

Insights

This study found that while etanercept use increases the risk of four adverse events in rheumatoid arthritis patients, this relative risk is similar for both elderly and non-elderly individuals. The study highlights age-independent safety profiles for etanercept concerning these specific adverse events.

Area of Science:

  • Rheumatology
  • Pharmacovigilance
  • Real-world evidence

Background:

  • Rheumatoid arthritis (RA) treatment involves medications like etanercept.
  • Elderly patients may have different risks for adverse events (AEs).
  • Four key AEs (congestive heart failure, serious infections, non-melanoma skin cancer, interstitial lung disease) were previously identified as important in RA patients.

Purpose of the Study:

  • To evaluate the interaction between age, etanercept treatment, and the risk of four specific AEs in RA patients using real-world data.
  • To compare the relative risk of these AEs between elderly (>65 years) and non-elderly (≤65 years) RA patients treated with etanercept.

Main Methods:

  • Utilized real-world data from the IBM Watson Health MarketScan Database (2013-2018).
  • Included RA patients aged ≥18 years with at least 1 year of enrollment prior to diagnosis and no prior AEs.
  • Employed propensity score matching and logistic regression to compare etanercept users and non-users, analyzing age as a key factor.

Main Results:

  • The overall cohort included 403,689 patients.
  • Absolute risk for all four AEs increased with age.
  • Etanercept was associated with significantly higher odds of all four AEs (p<0.001).
  • Crucially, the relative risk of these AEs with etanercept was similar between patients ≤65 years and >65 years.

Conclusions:

  • In RA patients, the relative increase in risk for congestive heart failure, serious infection, non-melanoma skin cancer, or interstitial lung disease associated with etanercept is consistent across elderly and non-elderly populations.
  • Age does not appear to modify the relative safety profile of etanercept concerning these specific adverse events.

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