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

  • Christopher J. EdwardsEmail author
  • Jack F. Bukowski
  • Sara M. Burns
  • Heather E. Jones
  • Ron Pedersen
  • Joan Sopczynski
  • Lisa Marshall
Original Research Article
  • 145 Downloads

Abstract

Objective

The aim of this study was to use real-world data to evaluate potential interactions between age, treatment, and the risk of developing four adverse events (AEs) common in the elderly: congestive heart failure, serious infections, non-melanoma skin cancer, and interstitial lung disease. These AEs were identified as important in a prior age-based analysis (≤ 65 vs > 65 years) of etanercept- or placebo-treated patients with rheumatoid arthritis (RA) in controlled clinical trials.

Methods

Real-world data (1 January 2013 to 31 January 2018) were obtained from the IBM Watson Health MarketScan® Database. Patients were included if aged ≥ 18 years, enrolled for ≥ 1 year prior to RA diagnosis, and without any of the four AEs of interest prior to RA diagnosis or between RA diagnosis and first etanercept exposure. Logistic regression analysis was applied following propensity matching of patients receiving or not receiving etanercept based on age at diagnosis, age status at the beginning of observation (> 65 years or not), sex, geographic region, and follow-up duration.

Results

The overall cohort comprised 403,689 patients. The absolute risk of each of the four AEs increased with age. In propensity-matched cohorts, etanercept was associated with significantly higher odds of developing each of the four AEs (p < 0.001 for all). However, the relative risk of experiencing the four AEs in patients who received etanercept versus those who did not was similar between patients ≤ 65 years of age and those > 65 years of age.

Conclusions

In patients with RA, the relative increase in etanercept-associated risk of experiencing congestive heart failure, serious infection, non-melanoma skin cancer, or interstitial lung disease was similar between elderly and non-elderly.

Notes

Acknowledgements

This study was funded by Pfizer. Medical writing support was provided by David Wateridge, PhD, and Lorna Forse, PhD, of Engage Scientific Solutions, and was funded by Pfizer.

Compliance with Ethical Standards

Funding

This study was sponsored by Pfizer.

Conflict of interest

CJE has received research grants from AbbVie and Pfizer, and consultant fees from AbbVie, Celgene, Janssen, MSD, Pfizer, Roche, Samsung, Sanofi and UCB. JFB, SB, HEJ, RP, JS and LM are employees of Pfizer, or were employees of Pfizer when this study was conducted, and hold stock or stock options in Pfizer.

Ethical approval

As a non-interventional study, ethical approval was not required for this analysis. This article does not contain any studies with human participants or animals performed by any of the authors.

Supplementary material

40266_2019_721_MOESM1_ESM.pdf (48 kb)
Supplementary material 1 (PDF 47 kb)

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Copyright information

© Springer Nature Switzerland AG 2019

Authors and Affiliations

  • Christopher J. Edwards
    • 1
    Email author
  • Jack F. Bukowski
    • 2
  • Sara M. Burns
    • 3
  • Heather E. Jones
    • 2
  • Ron Pedersen
    • 2
  • Joan Sopczynski
    • 2
  • Lisa Marshall
    • 2
  1. 1.Rheumatology Department, NIHR Clinical Research FacilityUniversity Hospital Southampton NHS Foundation TrustSouthamptonUK
  2. 2.PfizerCollegevilleUSA
  3. 3.PfizerCambridgeUSA

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