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Rituximab for Treatment of Non-infectious and Non-malignant Orbital Inflammatory Disease

Overview
Publisher Springer
Specialty Ophthalmology
Date 2021 Aug 27
PMID 34448063
Citations 4
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Abstract

Purpose: To provide a comprehensive review of rituximab use for the treatment of non-infectious/non-malignant orbital inflammation.

Methods: Review of literature through January 2021.

Results: Individual data was available for 167 patients with refractory non-infectious/non-malignant orbital inflammation who received treatment with rituximab (RTX). Rituximab was generally utilized as third-line or later treatment (108/149, 72.5%) at a mean of 44.6 months following the diagnosis of orbital inflammation (range = 0 to 360 months; median = 13.7 months). Patients with non-infectious/non-malignant orbital inflammation either received prior treatment with corticosteroids only (27/122, 22.1%), or with one (31/122, 25.4%), two (25/122, 20.5%), or three or more (25/122, 20.5%) corticosteroid-sparing immunosuppressive agents with or without corticosteroids before initiation of RTX treatment. The rheumatologic protocol (two infusions of 1 gram of RTX separated by 14 days) was utilized most frequently (80/144, 55.6%), followed by the oncologic protocol (four weekly infusions of 375 mg/m RTX; 51/144, 35.4%). Various other off-label regimens were used infrequently (13/144, 9.0%). Rituximab treatments resulted in a positive therapeutic response for the majority of patients with orbital inflammation (146/166, 88.0%). Commonly treated diagnoses included granulomatosis with polyangiitis (99/167, 59.3%), IgG-4 related disease (36/167, 21.6%), and orbital inflammation of indeterminate cause (25/167, 15.0%). No side effects were reported in 83.3% (55/66) of cases. The most common RTX-induced adverse event was an infusion-related temporary exacerbation of orbital disease (4/66, 6.1%), which occurred prior to the routine use of systemic corticosteroids as pre-conditioning.

Conclusions: Overall, RTX appears to be both efficacious and well-tolerated as second- or third-line therapy for patients with non-infectious/non-malignant orbital inflammation.

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Orbital inflammatory disease: a joint clinical experience in rheumatology and ophthalmology.

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Nonspecific Orbital Inflammation (NSOI): Unraveling the Molecular Pathogenesis, Diagnostic Modalities, and Therapeutic Interventions.

Wu K, Kulbay M, Daigle P, Nguyen B, Tran S Int J Mol Sci. 2024; 25(3).

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References
1.
Babu K, Dharmanand B . Worsening of posterior scleritis and orbital pseudotumor in a patient with granulomatosis polyangiitis with rituximab-A case report. Indian J Ophthalmol. 2020; 68(9):1986-1988. PMC: 7690530. DOI: 10.4103/ijo.IJO_1644_20. View

2.
Aries P, Hellmich B, Voswinkel J, Both M, Nolle B, Holl-Ulrich K . Lack of efficacy of rituximab in Wegener's granulomatosis with refractory granulomatous manifestations. Ann Rheum Dis. 2005; 65(7):853-8. PMC: 1798224. DOI: 10.1136/ard.2005.044420. View

3.
Laban K, Kalmann R, Leguit R, de Keizer B . Zirconium-89-labelled rituximab PET-CT in orbital inflammatory disease. EJNMMI Res. 2019; 9(1):69. PMC: 6667535. DOI: 10.1186/s13550-019-0530-9. View

4.
Khosroshahi A, Bloch D, Deshpande V, Stone J . Rituximab therapy leads to rapid decline of serum IgG4 levels and prompt clinical improvement in IgG4-related systemic disease. Arthritis Rheum. 2010; 62(6):1755-62. DOI: 10.1002/art.27435. View

5.
Pelegrin L, Jakob E, Schmidt-Bacher A, Schwenger V, Becker M, Max R . Experiences with rituximab for the treatment of autoimmune diseases with ocular involvement. J Rheumatol. 2013; 41(1):84-90. DOI: 10.3899/jrheum.130206. View