Long-term Safety and Efficacy of Reslizumab in Patients with Eosinophilic Asthma

J Allergy Clin Immunol Pract. 2017 Nov-Dec;5(6):1572-1581.e3. doi: 10.1016/j.jaip.2017.08.024.

Abstract

Background: In placebo-controlled trials, reslizumab, an anti-IL-5 monoclonal antibody, significantly reduced asthma exacerbations and improved lung function and asthma control in patients with eosinophilic asthma.

Objective: This open-label extension study evaluated safety and efficacy of reslizumab for up to 24 months.

Methods: After participation in 1 of 3 placebo-controlled, phase III trials in moderate-to-severe eosinophilic asthma, patients received reslizumab 3.0 mg/kg intravenously every 4 weeks for up to 24 months. Adverse events (AEs), lung function, and patient-reported asthma control were evaluated.

Results: In the open-label extension, 1,051 patients received ≥1 reslizumab dose (480 reslizumab-naïve, 571 reslizumab-experienced); median (range) exposure was 319 (36-840) and 343 (36-863) days in reslizumab-naïve and reslizumab-experienced patients, respectively. Continuous exposure, including during the placebo-controlled studies, was ≥12 months for 740 patients and ≥24 months for 249 patients. The most common AEs were worsening of asthma and nasopharyngitis. Serious AEs affected 78 of 1,051 (7%) patients; 18 of 1,051 (2%) discontinued treatment because of AEs; and there were 3 deaths (all non-treatment-related). Fifteen adult patients (15 of 1,023; 1%) had malignancies of diverse tissue types. Reslizumab-experienced patients maintained improved lung function and asthma control; reslizumab-naïve patients had improvements in these measures throughout open-label treatment. Blood eosinophil counts appeared to be returning to baseline after reslizumab discontinuation.

Conclusions: In patients with moderate-to-severe eosinophilic asthma, intravenous reslizumab 3.0 mg/kg displays favorable long-term safety and sustained long-term efficacy. Initial improvements in lung function and asthma control were maintained for up to 2 years. These findings substantially add to our understanding of the long-term safety and efficacy of anti-IL-5 strategies.

Keywords: Anti-IL-5; Asthma; Eosinophil; Long-term safety; Open-label extension study; Reslizumab.

Publication types

  • Clinical Trial
  • Multicenter Study

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Anti-Asthmatic Agents / adverse effects
  • Anti-Asthmatic Agents / therapeutic use*
  • Antibodies, Monoclonal, Humanized / adverse effects
  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • Asthma / drug therapy*
  • Asthma / mortality
  • Child
  • Eosinophils / drug effects
  • Eosinophils / immunology*
  • Female
  • Follow-Up Studies
  • Humans
  • Immunotherapy / adverse effects
  • Immunotherapy / methods*
  • Interleukin-5 / immunology
  • Male
  • Middle Aged
  • Nasopharyngitis / drug therapy*
  • Nasopharyngitis / mortality
  • Neoplasms / etiology
  • Respiratory Function Tests
  • Survival Analysis
  • Young Adult

Substances

  • Anti-Asthmatic Agents
  • Antibodies, Monoclonal, Humanized
  • Interleukin-5
  • reslizumab