Racial/ethnic differences in treatment efficacy and safety for moderate-to-severe plaque psoriasis: a systematic review

Arch Dermatol Res. 2023 Jan;315(1):41-50. doi: 10.1007/s00403-022-02324-4. Epub 2022 Jan 20.

Abstract

Biologic medications have revolutionized treatment of psoriasis; however, there remains uncertainty in which medications should be used to maximize efficacy based on race/ethnicity. The purpose was to determine if efficacy of biological medications differs based on race/ethnicity. A systematic review identified all clinical trials focused on biologic treatment outcomes from inception of database until March 5th, 2021. Included studies provided data on racial/ethnic differences in biologic skin clearance efficacy using the Psoriasis Area and Severity Index (PASI) and "clear/almost clear" scores. There were 1220 studies identified, and 24 included in the review. The races/ethnicities included were Asian (n = 2740), White (n = 9745), Black (n = 138), and Latino (n = 728). Ixekizumab provided the highest "clear/almost clear" score (90.7%, 89.4%) and PASI 75 (98.8%, 96.6%) for Asian and Latino patients, respectively. Guselkumab had the highest "clear/almost clear" score for White (86.8%) patients, while Black patients had highest "clear/almost clear" (75.0%) and PASI 75 (91.7%) scores to brodalumab. Limitations included lack of studies reporting outcome data based on race/ethnicity and lack of patients of color within psoriasis clinical trials. For treatment of plaque psoriasis, there is evidence of differences in efficacy of biologics improving clinical disease severity between different races or ethnicities.

Keywords: Biologics; Efficacy; Plaque psoriasis; Safety; Skin of color; Systematic review.

Publication types

  • Systematic Review

MeSH terms

  • Antibodies, Monoclonal* / therapeutic use
  • Ethnicity
  • Healthcare Disparities*
  • Humans
  • Psoriasis* / chemically induced
  • Psoriasis* / drug therapy
  • Racial Groups
  • Severity of Illness Index
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal