Anti-IL6-Receptor Tocilizumab in Refractory and Noninfectious Uveitic Cystoid Macular Edema: Multicenter Study of 25 Patients
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Vegas Revenga, Nuria; Calvo Río, Vanesa; Mesquida, Marina; Adán, Alfredo; Hernández, María Victoria; Beltrán, Emma; Valls Pascual, Elia; Díaz-Valle, David; Díaz-Cordovés, Gisela; Hernandez-Garfella, Marisa; González Vela, María del Carmen; Aurrecoechea Aguinaga, Elena; Domínguez Casas, Lucía Cristina; Atienza Mateo, Belén; Martín Varillas, José Luis; Loricera García, Javier; Palmou Fontana, Natalia; Hernández Hernández, José Luis; González-Gay Mantecón, Miguel Ángel; [et al.]Fecha
2019-04Derechos
© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license
Publicado en
Am J Ophthalmol. 2019 Apr;200:85-94
Editorial
Elsevier
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Palabras clave
Cystoid Macular Edema
Uveitis
Anti-TNF Therapy
Tocilizumab
Resumen/Abstract
PURPOSE:
Cystoid macular edema (CME) is a leading cause of blindness. This study assessed the efficacy and safety of tocilizumab (TCZ) in refractory CME.
DESIGN:
Retrospective case series.
METHODS:
Patients with CME secondary to noninfectious uveitis who had inadequate response to corticosteroids and at least 1 conventional immunosuppressive drug, and in most cases to other biological agents, were studied. CME was defined as central retinal thickness greater than 300 ?m. The primary outcome measure was macular thickness. Intraocular inflammation, best-corrected visual acuity (BCVA), and corticosteroid-sparing effect were also analyzed.
RESULTS:
A total of 25 patients (mean ± standard deviation age 33.6 ± 18.9 years; 17 women) with CME were assessed. Underlying diseases associated with uveitis-related CME are juvenile idiopathic arthritis (n = 9), Behçet disease (n = 7), birdshot retinochoroidopathy (n = 4), idiopathic (n = 4), and sarcoidosis (n = 1). The ocular patterns were panuveitis (n = 9), anterior uveitis (n = 7), posterior uveitis (n = 5), and intermediate uveitis (n = 4). Most patients had CME in both eyes (n = 24). TCZ was used in monotherapy (n = 11) or combined with conventional immunosuppressive drugs. Regardless of the underlying disease, compared to baseline, a statistically significant improvement in macular thickness (415.7 ± 177.2 vs 259.1 ± 499.5 ?m; P = .00009) and BCVA (0.39 ± 0.31 vs 0.54 ± 0.33; P = .0002) was obtained, allowing us to reduce the daily dose of prednisone (15.9 ± 13.6 mg/day vs 3.1 ± 2.3 mg/day; P = .002) after 12 months of therapy. Remission was achieved in 14 patients. Only minor side effects were observed after a mean follow-up of 12.7 ± 8.34 months.
CONCLUSION:
Macular thickness is reduced following administration of TCZ in refractory uveitis-related CME.
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