Thyroid eye disease (TED) or Graves ophthalmopathy is a debilitating autoimmune disorder of the orbit. This disease is closely associated with autoimmune hyperthyroidism, although it may develop in the euthyroid and hypothyroid states. TED affects approximately 16 women and 3 men in every 100,000 per year. 1 Orbital radiotherapy (OR) is a well-established therapy that has been safely utilized in the treatment of TED for over a century, yet high-level randomized evidence supporting its efficacy and clear treatment guidelines are sparse. This article summarizes the existing literature regarding the use of OR in TED and associated outcomes and toxicities. We also discuss emerging treatment techniques and potential future therapeutic strategies.
' BackgroundThe pathogenesis of TED is attributable to an autoimmune interaction between antithyrotropin receptor antibodies and thyrotropin receptors expressed in the orbit. In the diseased state, the thyrotropin receptor is degraded by antigen-presenting cells resulting in the activation of T-helper cells. Plasma cells are then activated through cytokine interactions to secrete autoantibodies directed against the thyrotropin receptor in the orbit. 1 The result is a progressive orbital inflammatory and fibrotic process. This presents clinically with varying degrees of eyelid retraction, lagophthalmos, proptosis, impaired extraocular motility, diplopia, exposure keratopathy, and periorbital edema. Symptoms may be self-limited or progressive and debilitating, persisting for years despite aggressive therapy. In severe cases, sight-threatening corneal ulceration or compressive optic neuropathy may develop.