The risk of interstitial lung disease during biological treatment in Japanese patients with psoriasis

Clin Exp Dermatol. 2020 Oct;45(7):853-858. doi: 10.1111/ced.14259. Epub 2020 Jun 29.

Abstract

Background: With the increasing use of biological agents for the treatment of psoriasis, the numbers of patients with interstitial lung disease (ILD) associated with biologics have also increased. Many of these cases were associated with tumour necrosis factor (TNF)-α inhibitors, but cases associated with other families of biologics have also been reported in Japan.

Aim: To analyse the background factors of patients who developed ILD, and to discuss better management of biological treatment.

Method: We reviewed 246 patients with psoriasis who were treated with biological agents in our department to identify any pulmonary adverse events (AEs). Data on patients who developed ILD were extracted to analyse background factors, clinical type of psoriasis, time to onset of ILD, pre-existing ILD, smoking habit and prescribed drugs.

Results: Pulmonary AEs were seen in 22 cases, of which 11 were diagnosed as drug-induced ILD. The causative drugs were mainly TNF-α inhibitors, accounting for eight cases (six treated with infliximab, two with adalimumab). The remaining three cases were associated with secukinumab, ustekinumab and ixekizumab (n = 1 each). Notably, these three cases also had a history of drug-induced ILD.

Conclusion: Patients with a history of drug-induced ILD seem to be more susceptible to developing another ILD induced by biologics, even if treated with interleukin-17 inhibitors. Thorough screening of risk factors and evaluation for eligibility, and careful monitoring during treatment are the best solutions to avoid serious pulmonary AE. Early detection and precise diagnosis of pulmonary AEs, especially differentiation from infectious diseases, is essential for managing biological treatment.

Publication types

  • Review

MeSH terms

  • Adalimumab / adverse effects
  • Adult
  • Aged
  • Antibodies, Monoclonal, Humanized / adverse effects
  • Antirheumatic Agents / adverse effects
  • Biological Factors / adverse effects*
  • Biological Factors / therapeutic use
  • Early Diagnosis
  • Female
  • Humans
  • Infliximab / adverse effects
  • Japan / epidemiology
  • Lung Diseases, Interstitial / chemically induced*
  • Lung Diseases, Interstitial / epidemiology
  • Lung Diseases, Interstitial / prevention & control
  • Male
  • Middle Aged
  • Mucin-1 / blood
  • Psoriasis / complications
  • Psoriasis / drug therapy*
  • Psoriasis / pathology
  • Risk Factors
  • Tumor Necrosis Factor Inhibitors / adverse effects*
  • Ustekinumab / adverse effects

Substances

  • Antibodies, Monoclonal, Humanized
  • Antirheumatic Agents
  • Biological Factors
  • MUC1 protein, human
  • Mucin-1
  • Tumor Necrosis Factor Inhibitors
  • Infliximab
  • ixekizumab
  • secukinumab
  • Ustekinumab
  • Adalimumab