Efficacy and Safety of Anti-TNFα Therapy for Uveitis Associated with Juvenile Idiopathic Arthritis: A Systematic Review and Meta-Analysis.

Rheumatol Ther

Department of Rheumatology and Immunology, National Clinical Research Center for Child Health and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, Ministry of Education Key Laboratory of Child Development and Disorders, Children's Hospital of Chongqing Medical University, Chongqing, China.

Published: June 2021

AI Article Synopsis

  • The study aimed to evaluate how effective and safe anti-TNFα therapy is in treating patients with juvenile idiopathic arthritis associated uveitis (JIA-U).
  • Researchers analyzed data from multiple sources and included various types of studies, finding that adalimumab (ADA) had the highest control of intraocular inflammation (CII) at 82%, compared to other anti-TNFα treatments like infliximab (IFX), etanercept (ETA), and golimumab (GLM).
  • The results indicated that ADA is more effective and safer than IFX, while IFX is more effective than ETA, and there’s limited data on GLM and certolizumab pegol (CZP) showing

Article Abstract

Introduction: To investigate the efficacy and safety of anti-TNFα therapy in patients with juvenile idiopathic arthritis associated uveitis (JIA-U).

Methods: Embase, PubMed, Cochrane Library, and Web of Science were systematically searched for studies reporting anti-TNFα treatment in patients with JIA-U. The primary outcome was the control of intraocular inflammation (CII). The pooled proportion of CII was assessed by the random-effects method when I > 50%, otherwise, by the fixed-effect method. This study was registered with PROSPERO (CRD42020161749).

Results: Three randomized clinical trials (RCTs), twelve case series, three retrospective cohort studies, and three case reports were identified. A total of 399 patients were receiving anti-TNFα therapy, of which 201 patients were treated with adalimumab (ADA), 139 with infliximab (IFX), 36 with etanercept (ETA), 20 with golimumab (GLM), and 3 with certolizumab pegol (CZP). The pooled proportions of CII on observational studies were 82% (95% CI 63-96%) in patients receiving ADA, 56% (95% CI 30-80%) in IFX, 38% (95% CI 8-73%) in ETA and 65% (95% CI 42-86%) in GLM, respectively. All three patients treated with CZP reached improved activity. ADA therapy led to a significantly higher proportion of CII compared to IFX therapy (χ = 26.24, P < 0.001), or to ETA therapy (χ = 13.43, P < 0.001); but no statistical difference was observed between IFX and ETA (χ = 0.13, P = 0.71). As to safety, most reported adverse events were tolerable and two cohort studies consistently showed that ADA was safer than IFX.

Conclusions: The existing evidence suggests that ADA is better than IFX regarding efficacy and safety. The effectiveness of IFX is higher than ETA with no statistical difference. GLM and CZP may be proxies for ADA but the evidence is limited.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217376PMC
http://dx.doi.org/10.1007/s40744-021-00296-xDOI Listing

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