Graves' Orbitopathy (GO) is a disabling and disfiguring condition associated with Graves' Disease, due to autoimmunity against antigens expressed by the thyroid and orbital tissues, and resulting in orbital fibroblast proliferation and release of glycosaminoglycans. The current treatments available, especially glucocorticoids, are not effective in all patients. Two cases of patients with GO treated with Sirolimus have been reported with an excellent response to the drug. The rationale for the use of Sirolimus lies in its mechanisms of action. Sirolimus is able to inhibit T-cell activation as well as fibroblast proliferation. In addition, acts indirectly on the Insulin-Like Growth Factor-1 (IGF-1) pathway, and recent clinical trials have shown that a monoclonal antibody against the IGF-1 receptor (Teprotumumab) is effective in patients with GO. Thus, Sirolimus could be used in GO as monotherapy in patients with GO. The aim of the present drug vs standard treatment, observational study is to evaluate the efficacy of Sirolimus as a second-line treatment in patients with moderately severe, active GO.
Study Design: observational Thirty consecutive patients with moderate-to-severe and active GO treated with sirolimus (15 patients) or methylprednisolone (15 patients) observance 18 consecutive months will be compared. Study Timeline Baseline visit - (Time 0) Treatment period (week 1-week 12): daily administration of the trial agent (Sirolimus) or weekly administration of the standard treatment (methylprednisolone) Outcome visit (week 24)
Study Type
OBSERVATIONAL
Enrollment
30
2 mg orally on the first day followed by 0.5 mg per day for 12 weeks
500 mg/weekly (6 weeks) intravenously, 250 mg/weekly (6 weeks) (cumulative dose 4.5 g).
Endocrinologia II
Pisa, PI, Italy
GO overall response
Percentage of subjects with at least two of the following compared to baseline: a) Improvement in clinical activity score (CAS) by at least 1 point ; b) Improvement in exophthalmos by at least 2 mm; c) Improvement in lid aperture by at least 2 mm; d) Improvement in eye muscle ductions ≥8 degrees; e) Improvement of visual acuity by at least 0.2/1, without worsening of any of these parameters in the contralateral eye if applicable.
Time frame: 24 weeks
Change in exophthalmos
Percentage of subjects with a reduction greater than or equal to 2 mm compared with the baseline evaluation in the study eye, without worsening in the contralateral eye
Time frame: 24 weeks
Change in the clinical activity score (CAS)
Percentage of subjects with a reduction of CAS by at least two points in the study eye, without worsening in the contralateral eye
Time frame: 24 weeks
Change in quality of life
Comparison of the quality of life scores between the two groups, determined with a questionnaire specific for GO (GO-QoL)
Time frame: 24 weeks
Change in eye ductions
Percentage of subjects with an increase in eye ductions at least 8 degrees
Time frame: 24 weeks
Change in eyelid aperture
Percentage of subjects with a reduction greater than or equal to 2 mm
Time frame: 24 weeks
Change in diplopia
Percentage with an improvement in diplopia
Time frame: 24 weeks
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