Dupilumab for the treatment of prurigo nodularis: A systematic review

Front Immunol. 2023 Jan 20:14:1092685. doi: 10.3389/fimmu.2023.1092685. eCollection 2023.

Abstract

Background: Conventional treatment techniques have limited efficacy and more side effects in the treatment of prurigo nodularis. The better alternative treatment option for better outcomes of the disease is dupilumab.

Objective: The objective of this study was to systematically review dupilumab-related treatment outcomes in prurigo nodularis.

Methods: Several databases like Embase, PubMed, Web of Science, and Cochrane library were searched for data acquisition on October 8, 2022. Based on Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines, 24 publications were included in this study.

Results: After 4,12,16 and more than 16 weeks of dupilumab treatment, 8.3% (n=5/60), 34.4% (n=11/32), 3.6% (n=2/56), and 45.3% (n=29/64) of patients had complete remission, respectively. In addition, 85.0% (n=51/60), 59.4% (n=19/32), 83.9% (n=47/56), and 43.8% (n=28/64) had partial remission, respectively. Moreover, 6.7% (n=4/60), 6.3% (n=2/32), 12.5% (n=7/56), and 10.9% (n=7/64) showed no remission, respectively, and significant reduction of numeric rating scale itch intensity (from 9.0 to 4.9, 2.1, 2.8, 0.9) was attained. There were no serious adverse events observed during treatment, but the most common event observed was conjunctivitis (12.6%, n=15/119).

Conclusions: Dupilumab has definite effectiveness and safety in prurigo nodularis treatment.

Systematic review registration: https://www.crd.york.ac.uk/PROSPERO, identifier (CRD42022365802).

Keywords: biologics; dupilumab; itch; prurigo nodularis; treatment.

Publication types

  • Systematic Review

MeSH terms

  • Antibodies, Monoclonal, Humanized / adverse effects
  • Humans
  • Prurigo* / chemically induced
  • Prurigo* / drug therapy
  • Pruritus / drug therapy
  • Treatment Outcome

Substances

  • dupilumab
  • Antibodies, Monoclonal, Humanized