Systematic review and meta-analysis of the current literature on tocilizumab in patients with refractory Takayasu arteritis

Front Immunol. 2023 Feb 8:14:1084558. doi: 10.3389/fimmu.2023.1084558. eCollection 2023.

Abstract

Objective: To present the pooled quantitative evidence of baseline characteristics and clinical outcomes of tocilizumab (TCZ) in patients with refractory Takayasu arteritis (TAK).

Methods: A comprehensive systematic review and meta-analysis was performed on all available studies retrieved from the MEDLINE, Embase, and Cochrane databases, using TCZ in patients with refractory TAK. We applied the commands metan and metaprop_one in Stata Software to pool overall estimates of continuous data and binomial data, respectively. A random-effects model was recruited for analysis.

Results: Nineteen studies with 466 patients were included in this meta-analysis. The mean age at implementation of TCZ was 34.32 years. Female sex and Numano Type V were the most prominent baseline characteristics. During the 12-month follow-up when receiving TCZ treatment, pooled CRP was 1.17 mg/L (95% confidence interval [CI] -0.18-2.52), pooled ESR was 3.54 mm/h (95% CI 0.51-6.58), and pooled glucocorticoid dose was 6.26 mg/d (95% CI 4.24-8.27). Approximately 76% (95% CI 58-87%) of patients achieved a decrease in glucocorticoid dosage. Meanwhile, patients with TAK had a remission rate of 79% (95% CI 69-86%), a relapse rate of 17% (95% CI 5-45%), an imaging progress rate of 16% (95% CI 9-27%), and a retention rate of 68% (95% CI 50-82%). Adverse events occurred in 16% (95% CI 5-39%) of patients, and infection was the most common adverse event, with a rate of 12% (95% CI 5-28%).

Conclusion: TCZ treatment can provide favorable outcomes in terms of inflammatory markers, steroid-sparing effects, clinical response, drug retention and minimizing adverse effects for patients with refractory TAK.

Keywords: Takayasu arteritis; baseline characteristic; clinical outcome; refractory; tocilizumab.

Publication types

  • Meta-Analysis
  • Systematic Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antibodies, Monoclonal, Humanized / adverse effects
  • Female
  • Glucocorticoids* / therapeutic use
  • Humans
  • Takayasu Arteritis* / drug therapy
  • Treatment Outcome

Substances

  • Glucocorticoids
  • tocilizumab
  • Antibodies, Monoclonal, Humanized

Grants and funding

This study was supported by the Science and Technology Department of Sichuan Province (Grant No. 2021JDRC0045 and 2021YFS0164); Post-Doctor Research Project, West China Hospital, Sichuan University (Grant No. 2021HXBH012); Clinical Research Incubation Project of West China Hospital, Sichuan University (Grant No. 2019HXFH038 and 2021HXFH018).