Anti-IL-6 Receptor Tocilizumab in Refractory Graves’ Orbitopathy: National Multicenter Observational Study of 48 Patients

Autor: Marcelino Revenga, Valvanera Pinillos, Ángel García-Aparicio, Margarita Sánchez-Orgaz, Vanesa Calvo-Río, L. Sanchez-Bilbao, Belén Atienza-Mateo, Santos Castañeda, Ricardo Blanco, Elia Valls-Pascual, Beatriz Valls-Espinosa, Ana Blanco, Ángel Mora, José L. Hernández, Verónica Rodriguez-Mendez, Eva Tomero, D. Martínez-López, Diana Peiteado, Vega Jovaní, I. González-Mazón, O. Maiz-Alonso, M. Fernandez-Prada, Arantxa Conesa, Raúl Veroz-González, Juan A. Troyano, Miguel A. González-Gay, Elena Aurrecoechea, R. Demetrio-Pablo, I. Torre-Salaberri, Ángel López-Vázquez, Francisco J. Toyos-Sáenz de Miera
Přispěvatelé: UAM. Departamento de Medicina, Instituto de Investigación Sanitaria Hospital Universitario de La Princesa (IIS-IP), Universidad de Cantabria
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Zdroj: Journal of Clinical Medicine
Volume 9
Issue 9
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Journal of Clinical Medicine, Vol 9, Iss 2816, p 2816 (2020)
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
Journal of clinical medicine 2020, 9, 2816
Biblos-e Archivo. Repositorio Institucional de la UAM
UCrea Repositorio Abierto de la Universidad de Cantabria
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
ISSN: 2077-0383
DOI: 10.3390/jcm9092816
Popis: Graves&rsquo
orbitopathy (GO) is the most common extrathyroidal manifestation of Graves&rsquo
disease (GD). Our aim was to assess the efficacy and safety of Tocilizumab (TCZ) in GO refractory to conventional therapy. This was an open-label multicenter study of glucocorticoid-resistant GO treated with TCZ. The main outcomes were the best-corrected visual acuity (BVCA), Clinical Activity Score (CAS) and intraocular pressure (IOP). These outcome variables were assessed at baseline, 1st, 3rd, 6th and 12th month after TCZ therapy onset. The severity of GO was assessed according to the European Group on Graves&rsquo
Orbitopathy (EUGOGO). We studied 48 (38 women and 10 men) patients (95 eyes)
mean age ±
standard deviation 51 ±
11.8 years. Before TCZ and besides oral glucocorticoids, they had received IV methylprednisolone (n = 43), or selenium (n = 11). GO disease was moderate (n =29) or severe (n = 19) and dysthyroid optic neuropathy (DON) (n = 7). TCZ was used in monotherapy (n = 45) or combined (n = 3) at a dose of 8 mg/kg IV every four weeks (n = 43) or 162 mg/s.c. every week (n = 5). TCZ yielded a significant improvement in all of the main outcomes at the 1st month that was maintained at one year. Comparing the baseline with data at 1 year all of the variables improved
BCVA (0.78 ±
0.25 vs. 0.9 ±
0.16
p = 0.0001), CAS (4.64 ±
1.5 vs. 1.05 ±
1.27
p = 0.0001) and intraocular pressure (IOP) (19.05 ±
4.1 vs. 16.73 ±
3.4 mmHg
p = 0.007). After a mean follow-up of 16.1 ±
2.1 months, low disease activity (CAS &le
3), was achieved in 88 eyes (92.6%) and TCZ was withdrawn in 29 cases due to low disease activity (n = 25) or inefficacy (n = 4). No serious adverse events were observed. In conclusion, TCZ is a useful and safe therapeutic option in refractory GO treatment.
Databáze: OpenAIRE