Abstract | PURPOSE: METHODS:
Rituximab was administered intravenously, 1000 mg twice at a 2-week interval. The primary end point was a clinical activity score reduction (improvement by ⩾ 2 points or disease inactivation: clinical activity score < 3) at 24 weeks. Secondary end points included clinical activity score improved by ⩾ 2 points or inactivation of Graves' ophthalmopathy at 12 weeks, improvement in each item of the clinical activity score, in proptosis, in severity disease by the total eye score and in diplopia according to the Gorman score. RESULTS: A limited improvement in clinical activity score was observed (median improvement at 24 weeks by 1 point, p = 0.002, (5/14 patients, 35.7%). Disease inactivation occurred in 50% of patients (7/14 patients). At 12 weeks, clinical activity score improved by ⩾ 2 points in 2/14 patients (14.3%) and inactivation of Graves' ophthalmopathy occurred in four patients (28.6%). Improvement in proptosis and total eye score was observed in 3/9 patients (33%) and in 4/14 patients (28.6%) at 24 weeks, respectively. Only one patient experienced moderate adverse event. CONCLUSION:
Rituximab is a well-tolerated treatment with a good safety profile, but offered limited and partial improvement for active moderate-to-severe Graves' ophthalmopathy with a long duration of disease.
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Authors | Laura Eid, Valentine Coste-Verdier, Eric Longueville, Emmanuel Ribeiro, Bogdan Nicolescu-Catargi, Jean-François Korobelnik |
Journal | European journal of ophthalmology
(Eur J Ophthalmol)
Vol. 30
Issue 5
Pg. 1008-1013
(Sep 2020)
ISSN: 1724-6016 [Electronic] United States |
PMID | 31025590
(Publication Type: Journal Article)
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Chemical References |
- Immunologic Factors
- Rituximab
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Topics |
- Aged
- Diplopia
(physiopathology)
- Female
- Follow-Up Studies
- Graves Ophthalmopathy
(drug therapy, physiopathology)
- Humans
- Immunologic Factors
(therapeutic use)
- Infusions, Intravenous
- Kidney Function Tests
- Liver Function Tests
- Lymphocyte Count
- Male
- Middle Aged
- Retrospective Studies
- Rituximab
(therapeutic use)
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