Abstract

BackgroundAlthough fluorescein angiography (FA) is a frequently used imaging modality in patients with non-infectious uveitis (NIU), it has not been reliably used for objective assessment of posterior segment inflammatory outcomes in these patients. In this index study we report the posterior segment inflammatory outcomes of two different doses of intravenous (IV) infusions of tocilizumab (TCZ), an IL-6 inhibitor, in eyes with NIU using a semi-quantitative FA scoring system.MethodsSTOP-Uveitis is a randomized, multi-center clinical trial conducted at 5 clinical centers across the United States. The study evaluated the role of TCZ in patients with NIU. Thirty-seven (37) patients with NIU were randomized into one of two treatment groups in a ratio of 1:1. Group 1 received IV infusions of 4 mg/kg TCZ and group 2 received IV infusions of 8 mg/kg TCZ. Infusions were given every 4 weeks in both groups until month 6 (primary endpoint). Posterior segment inflammatory outcomes were assessed by evaluating FA at baseline and month 6 by graders at a central reading center. A previously reported, semi-quantitative, scoring system for FA was used to assess signs that represent ongoing inflammatory processes in the posterior segment. These signs included optic disc hyperfluorescence, macular edema, retinal vascular staining and/or leakage, capillary leakage, retinal capillary nonperfusion, neovascularization of the optic disc, neovascularization elsewhere, pinpoint leaks, and retinal staining and/or subretinal pooling. Statistical significance was set at p < 0.05. Main outcome measures included change in posterior segment inflammation as assessed using FA at month 6.Results37 eyes (37 patients) were randomized in the STOP-Uveitis study. 30 eyes were found to be eligible for this sub-study based on study criteria. Seven eyes had ungradable images at either baseline or month 6 and were therefore excluded from the analysis. The reduction in FA inflammatory scores at month 6 were statistically significant in both groups (p < 0.05). The difference between the two groups was not significant (p = 0.351).ConclusionsIV infusions of tocilizumab (both 4 and 8 mg/kg) are effective in improving posterior segment inflammation in eyes with NIU. A semi-quantitative FA scoring system may be used as a reliable outcome measure for assessment of posterior segment inflammation.ClinicalTrials.gov Identifier: NCT01717170

Highlights

  • Fluorescein angiography (FA) is a frequently used imaging modality in patients with noninfectious uveitis (NIU), it has not been reliably used for objective assessment of posterior segment inflammatory outcomes in these patients

  • TCZ is a recombinant humanized monoclonal antibody directed against IL-6; which is a pro-inflammatory cytokine with a proven role in immune mediated diseases such as uveitis

  • We have previously reported favorable outcomes of patients with non-infectious uveitis (NIU) treated with TCZ in the STOP-Uveitis study [2, 13]

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Summary

Introduction

Fluorescein angiography (FA) is a frequently used imaging modality in patients with noninfectious uveitis (NIU), it has not been reliably used for objective assessment of posterior segment inflammatory outcomes in these patients. In this index study we report the posterior segment inflammatory outcomes of two different doses of intravenous (IV) infusions of tocilizumab (TCZ), an IL-6 inhibitor, in eyes with NIU using a semi-quantitative FA scoring system. The Study of the safety, tolerability, and bioactivity of Tocilizumab On Patients with non-infectious Uveitis (STOP-Uveitis) study was the first multicenter, randomized, open label clinical trial evaluating two different doses of TCZ (4 mg/kg and 8 mg/kg) in patients with NIU. The study has previously reported a favorable safety and efficacy profile at the month 6 primary endpoint of the study [2]

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