Clinical Trial: Combined Radiotherapy and Intravenous Steroids for Early Progressive Thyroid Eye Disease

Study Status: Not yet recruiting
Recruit Status: Not yet recruiting
Study Type: Interventional

Official Title: Combined Radiotherapy and Intravenous Steroids for Early Progressive Thyroid Eye Disease

Brief Summary:

Thyroid eye disease is an autoimmune disorder affecting approximately 50% of individuals with autoimmune thyroid diseases resulting in enlargement of ocular muscles and may lead to congestion of the eyelids and ocular surface, ocular movement restriction and double vision, and optic nerve compression and loss of vision.

First line medical therapy is oral or intravenous corticosteroids (CS), which several studies have shown results in reduction of soft tissue congestion, but some studies suggesting that ocular restriction or visual loss may still occur in spite of CS therapy.i

External beam radiotherapy (XRT) is second line therapy but is controversial, with some studies suggesting benefit in preventing onset of double vision or optic nerve compression while other studies suggest it has no benefit. Most proponents of XRT for TED believe that it is most effective early in the disease evolution. XRT has been shown to be a safe therapy with few side-effects, although retinopathy changes have developed in a small percentage of diabetics and its use is avoided for diabetics.

Combined oral prednisone and XRT has been shown to be more effective in reducing soft tissue inflammation and motility complications than either monotherapy in two different studies.

To date there have been no trials comparing combined XRT and iv CS with iv CS alone for early progressive TED to identify potential benefit in reducing the severity of motility disorders or preventing the onset of dysthyroid optic neuropathy. That is the purpose of this study.


Detailed Summary:

  1. Purpose: To demonstrate that combined Radiotherapy (RT) and intravenous corticosteroid (CS) is more effective than iv CS alone in preventing severe motility disruption (including strabismus and primary diplopia) and new-onset dysthyroid optic neuropathy in early progressive thyroid orbitopathy.
  2. Hypothesis: Combined RT and iv CS are more effective than iv CS alone in preventing motility problems (reduced field of single binocular vision, reduced ductions, strabismus and worsening diplopia) and in preventing new-onset dysthyroid optic neuropathy in patients with early progressive thyroid orbitopathy.
  3. Justification: Standard therapy for progressive TED is iv CS, occasionally supplemented with RT if complications develop in spite of appropriate iv CS therapy. A single retrospective study suggested that early combined treatment may prevent more serious visual complications; this would be the first randomized controlled prospective trial to see if this finding is true.
  4. Objectives: Demonstrate a statistically significant reduced rate of new onset optic neuropathy and double vision in patients with progressive TED with combined therapy versus traditional monotherapy.
  5. Research Method: Multicentre, institutional based, randomized controlled trial.
  6. Statistical Analysis:

Subjects: 100 patients with early progressive TED randomized equally into two groups:

  1. Therapy: iv MP 500 mg iv weekly for 6 weeks, then 250 mg iv weekly for 6 weeks

    + XRT 100 Rads to each orbit x 10 doses

  3. New onset dysthyroid optic neuropathy [ Time Frame: 1 year ]
  4. Progression in ocular motility dysfunction (Improvement or worsening in motility scores and ocular restriction, and need for strabismus surgery) [ Time Frame: 1 year ]
    Improvement or worsening in motility scores and ocular restriction, and need for strabismus surgery at 1 year following initiation of treatment
  5. Participants escaping trial (Number of participants leaving trial because of onset of optic neuropathy or primary strabismus) [ Time Frame: 1 year ]
    Number of participants leaving trial because of onset of optic neuropathy or primary strabismus


    6. Original Primary Outcome: Same as current

    Current Secondary Outcome:

    • VISA inflammatory scores [ Time Frame: 6 months and 1 year ]
      Ocular Inflammatory and congestive scores
    • Quality of life scores [ Time Frame: 6 months and 1 year ]
      Specific Graves orbitopathy quality of life scoring systems: TED QOL and GO QOL
    • Proptosis and eyelid retraction changes [ Time Frame: 1 year ]
      Change in proptosis and upper lid retraction
    • Supplemental iv corticosteroid requirements [ Time Frame: 1 year ]
      Need for additional intravenous corticosteroids


    Original Secondary Outcome: Same as current

    Information By: University of British Columbia

    Dates:
    Date Received: January 12, 2015
    Date Started: January 2015
    Date Completion: December 2019
    Last Updated: January 14, 2015
    Last Verified: January 2015