AI Article Synopsis

  • This study reviewed the effectiveness of two biological drugs, adalimumab (ADA) and infliximab (IFX), in treating autoimmune uveitis.
  • A systematic search from 2014 to February 2022 identified six studies that met the criteria, which showed both drugs had similar effectiveness and side effects, though the studies were mainly non-randomized and had limitations.
  • The conclusion emphasizes that more high-quality, randomized controlled trials are necessary to better compare ADA and IFX for treating uveitis.

Article Abstract

Objective: This study aimed to review effectiveness studies comparing two biological anti-tumour necrosis factor agents, adalimumab (ADA) and infliximab (IFX), in the management of autoimmune uveitis.

Methods: A systematic search was conducted across PubMed, Scopus, Web of Science and Google Scholar from 2014 until February 2022. The search included the following keywords "Adalimumab", "Infliximab", "Autoimmune", "Anterior", "Intermediate", "Posterior", "Panuveitis", "Refractory" and "Uveitis". Primary studies comparing both ADA and IFX in a population of autoimmune uveitis patients were considered. Outcomes of interest were measures of response to treatment and incidence of adverse events.

Results: The preliminary literature search generated 7156 references. Six studies fulfilled the eligibility criteria and were included in the final analysis; all were non-randomised, retrospective or observational. The included studies found similar effectiveness and side effect profiles for both ADA and IFX in the management of autoimmune uveitis, however, one did not report effectiveness for each separately, and three were limited to Behcet's disease.

Conclusion: ADA and IFX seem to display comparable effectiveness and safety profiles. However, the available evidence remains scarce, of low quality and at high risk of bias. A direct comparison between ADA and IFX through large randomised controlled trials is needed to provide more substantial evidence of equivalence or superiority in uveitis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277136PMC
http://dx.doi.org/10.1136/bmjophth-2023-001303DOI Listing

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