4.6 Article

Adverse Health-Related Quality of Life Outcome Despite Adequate Clinical Response to Treatment in Systemic Lupus Erythematosus

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FRONTIERS IN MEDICINE
卷 8, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fmed.2021.651249

关键词

systemic lupus erythematosus; health-related quality of life; patient-reported outcome; fatigue; biologic drugs; patient perscpective

资金

  1. GlaxoSmithKline Investigator-Sponsored Studies (ISS) programme
  2. Swedish Rheumatism Association [R-932236]
  3. King Gustaf V's 80-year Foundation [FAI-2019-0635]
  4. Professor Nanna Svartz Foundation [2019-00290]
  5. Ulla and Roland Gustafsson Foundation [2019-12]
  6. Region Stockholm
  7. Karolinska Institutet

向作者/读者索取更多资源

The study revealed that despite achieving adequate clinical response with standard therapy plus belimumab or placebo, a substantial proportion of SLE patients still experienced adverse health-related quality of life (HRQoL) outcomes, with factors such as age, ethnicity, and organ damage contributing to these outcomes. Additional belimumab treatment was associated with lower frequencies of adverse physical functioning and fatigue, suggesting a potential protective effect in improving HRQoL in SLE patients.
Objective: To determine the prevalence of adverse health-related quality of life (HRQoL) outcomes in patients with SLE who achieved an adequate clinical response after a 52-week long standard therapy plus belimumab or placebo, and identify contributing factors. Methods: We included patients who met the primary endpoint of the BLISS-52 (NCT00424476) and BLISS-76 (NCT00410384) trials, i.e., SLE Responder Index 4 (total population: N = 760/1,684; placebo: N = 217/562; belimumab 1 mg/kg: N = 258/559; belimumab 10 mg/kg: N = 285/563). Adverse HRQoL outcomes were defined as SF-36 scale scores <= the 5th percentile derived from age- and sex-matched population-based norms, and FACIT-Fatigue scores Results: We found clinically important diminutions of HRQoL in SLE patients compared with matched norms and high frequencies of adverse HRQoL outcomes, the highest in SF-36 general health (29.1%), followed by FACIT-Fatigue (25.8%) and SF-36 physical functioning (25.4%). Overall, frequencies were higher with increasing age. Black/African American and White/Caucasian patients reported higher frequencies than Asians and Indigenous Americans, while Hispanics experienced adverse HRQoL outcome less frequently than non-Hispanics. Established organ damage was associated with adverse physical but not mental HRQoL outcomes; particularly, damage in the cardiovascular (OR: 2.12; 95% CI: 1.07-4.21; P = 0.032) and musculoskeletal (OR: 1.41; 95% CI: 1.01-1.96; P = 0.041) domains was associated with adverse SF-36 physical component summary. Disease activity showed no impact on HRQoL outcomes. In multivariable logistic regression analysis, addition of belimumab to standard therapy was associated with lower frequencies of adverse SF-36 physical functioning (OR: 0.59; 95% CI: 0.39-0.91; P = 0.016) and FACIT-F (OR: 0.53; 95% CI: 0.34-0.81; P = 0.004). Conclusions: Despite adequate clinical response to standard therapy plus belimumab or placebo, a substantial proportion of SLE patients still reported adverse HRQoL outcomes. While no impact was documented for disease activity, established organ damage contributed to adverse outcome within physical HRQoL aspects and add-on belimumab was shown to be protective against adverse physical functioning and severe fatigue.

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