Treatment of plaque psoriasis with IL-23p19 blockers: A systematic review and meta-analysis

Int Immunopharmacol. 2019 Oct:75:105841. doi: 10.1016/j.intimp.2019.105841. Epub 2019 Aug 26.

Abstract

Objectives: Interleukin(IL)-23 is a key cytokine in the pathogenesis of psoriasis, this meta-analysis was to analyze the efficacy and safety of IL-23p19 blockers in patients with plaque psoriasis.

Methods: A systematic review of the literature was performed to collect double-blind randomized controlled trials(RCTs). The pooled relative risk(RR) with 95% confidence interval(CI) was calculated. All analyses were conducted with intention-to-treat basis.

Results: A total of 13 studies contained 5155 plaque psoriasis patients were included in our meta-analysis. The results indicated that IL-23p19 blockers had better efficacy than placebo for Psoriasis Area Severity Index score reductions from baseline of 75% or more (PASI75) (RR = 11.47, P < 0.001) and static Physician's Global Assessment score of 0 or 1(sPGA0/1) (RR = 11.32, P < 0.001). IL-23p19 blockers have similar safety with placebo about the incidence of adverse events(AEs) (RR = 1.22, P = 0.096) and serious adverse events(SAEs) (RR = 2.93, P = 0.965), but IL-23p19 blockers carried an increased incidence rate of infections (RR = 1.39, P < 0.001). While compared with adalimumab and ustekinumab, IL-23p19 blockers were more effective and had the similar tolerance. Among three IL-23p19 blockers, guselkumab was the most efficacious treatments, and risankizumab was better tolerated than the others.

Conclusion: The IL-23p19 blockers have excellent efficacy and great safety in plaque psoriasis patients, but long-term safety remains to be determined.

Keywords: Guselkumab; IL-23p19; Meta-analysis; Psoriasis; Risankizumab; Tildrakizumab.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Antibodies, Monoclonal / therapeutic use*
  • Humans
  • Interleukin-23 Subunit p19 / antagonists & inhibitors*
  • Psoriasis / drug therapy*
  • Randomized Controlled Trials as Topic

Substances

  • Antibodies, Monoclonal
  • Interleukin-23 Subunit p19