Efficacy and Safety of IGF-1 Receptor Inhibitors for Thyroid Eye Disease: Systematic Review and Meta-analysis of Randomized Controlled Trials.

DrugsSep 24, 2026 (epub)
Clinical ResearchOphthalmologyEndocrinologyOpen access

Haiyang Zhang, Zixiang Zhang, Ting Lu et al.

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In 30 seconds

This systematic review and meta-analysis pooled randomized controlled trials comparing IGF-1 receptor inhibitors with placebo for thyroid eye disease (TED). Across 7 trials involving 669 patients, treatment improved several outcomes, including proptosis response (RR = 7.71, 95% CI 5.04-11.79, P < 0.001) and overall response (RR = 8.74, 95% CI 5.61-13.62, P < 0.001). Benefits were also reported for clinical activity, diplopia, proptosis change, and quality of life. Adverse events were more frequent with active treatment (RR = 1.15, 95% CI 1.06-1.24, P < 0.001); efficacy for proptosis reduction was greater in acute active TED.

Key findings

  • IGF-1 receptor inhibitors improved proptosis response versus placebo (RR = 7.71, 95% CI 5.04-11.79, P < 0.001).
  • Overall response was higher with inhibitors (RR = 8.74, 95% CI 5.61-13.62, P < 0.001).
  • Treatment was associated with greater proptosis reduction (MD = - 2.22 mm, 95% CI - 2.45 to - 1.99 mm, P < 0.001) and quality-of-life improvement (MD = 10.48, 95% CI 6.95-14.00, P < 0.001).
  • Pooled adverse-event rates were higher with active treatment (RR = 1.15, 95% CI 1.06-1.24, P < 0.001).

Why it matters

The pooled randomized evidence indicates that IGF-1 receptor inhibitors can improve multiple clinically relevant TED outcomes compared with placebo, while also increasing adverse events. The finding of greater proptosis-reduction efficacy in acute active disease may help frame expectations across disease activity states. Balancing these benefits against treatment-related harms is important when considering disease-modifying therapy.

What to keep in mind

The analysis included 7 trials and 669 patients; the abstract reports heterogeneity-related analyses but does not provide further detail on limitations.

Source

Published in Drugs. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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