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POS1340 (2021)
MULTICENTER STUDY OF 71 PATIENTS WITH REFRACTORY UVEITIS RELATED TO IMMUNE-MEDIATED INFLAMMATORY DISEASES ON CERTOLIZUMAB PEGOL TREATMENT
J. L. Martín-Varillas1, V. Calvo-Río2, L. Sanchez-Bilbao2, I. González-Mazón2, A. Adan3, I. Hernanz Rodríguez3, A. Gallego4, E. Beltrán5, S. Castro6, P. Fanlo7, A. García Martos8, I. Torre-Salaberri9, M. Cordero-Coma10, J. De Dios-Jiménez Aberásturi11, Á. García-Aparicio12, M. Hernández-Garfella13, A. Sanchez-Andrade14, A. García-Valle15, O. Maiz16, R. Miguélez17, S. Rodríguez Montero18, A. Urruticoechea-Arana19, R. Veroz Gonzalez20, A. Conesa21, C. Fernández-Carballido22, V. Jovani23, O. Martínez González24, P. Moya25, S. Romero-Yuste26, P. Rubio Muñoz27, E. Peña Sainz-Pardo28, M. A. González-Gay2, J. L. Hernández2, R. Blanco2
1Hospital Sierrallana, Rheumatology, Torrelavega, Spain
2H. U. Marqués de Valdecilla, Rheumatology, Santander, Spain
3H. Clinic, Ophthalmology, Barcelona, Spain
4H.U. de Badajoz, Rheumatology, Badajoz, Spain
5H. del Mar, Rheumatology, Barcelona, Spain
6H. U. Joan XXIII, Rheumatology, Tarragona, Spain
7C.H. de Navarra, Internal Medicine, Navarra, Spain
8H. U. del Tajo, Rheumatology, Madrid, Spain
9H. Basurto, Rheumatology, Bilbao, Spain
10C.A.U. de León, Ophthalmology, León, Spain
11H. U. de Álava, Rheumatology, Vitoria, Spain
12C.H.U. de Toledo, Rheumatology, Toledo, Spain
13H.G.U. de Valencia, Ophthalmology, Valencia, Spain
14H. Lucus Augusti, Rheumatology, Lugo, Spain
15C.A.U. de Palencia, Rheumatology, Palencia, Spain
16H.U. Donostia, Rheumatology, San Sebastian, Spain
17H. Móstoles, Rheumatology, Madrid, Spain
18H.U. Virgen de Valme, Rheumatology, Sevilla, Spain
19H. Can Misses, Rheumatology, Ibiza, Spain
20H. Merida, Rheumatology, Mérida, Spain
21H.G.U. de Castellón, Rheumatology, Castellón, Spain
22H. San Juan, Rheumatology, Alicante, Spain
23H.G.U. de Alicante, Rheumatology, Alicante, Spain
24H.C.U. de Salamanca, Rheumatology, Salamanca, Spain
25H. Santa Creu i Sant Pau, Rheumatology, Barcelona, Spain
26C.H.U. de Pontevedra, Rheumatology, Pontevedra, Spain
27H. de l’Esperit Sant, Rheumatology, Barcelona, Spain
28H.U. 12 de Octubre, Pediatrics, Madrid, Spain

Background: Prognosis of non-infectious refractory uveitis has improved markedly with biologic therapy (BT) (1-5 ). Most data are with monoclonal anti-TNF drugs, especially Adalimumab (ADA) and Infliximab (IFX). However, there is not enough evidence for the use of Certolizumab Pegol (CZP).


Objectives: To evaluate the efficacy and safety of CZP in refractory uveitis secondary to Immune-Mediated Inflammatory Diseases (IMID).


Methods: Multicenter study of 71 patients with uveitis due to IMID refractory to glucocorticoids and conventional immunosuppressants. Efficacy was assessed with the following ocular parameters: best corrected visual acuity (BCVA), anterior chamber cells, vitritis, macular thickness and presence of retinal vasculitis. These outcomes were compared between baseline, 1st week, 1st and 6th month, and 1st and 2nd year. Statistical analysis was performed with IBM SPSS Statistics v.23.


Results: 71 patients/100 affected eyes (29 men/42 women) with mean age of 40.0±11.3 years were studied. Underlying IMIDs were: spondyloarthritis (n=38), Behçet (10), psoriatic arthritis (8), Crohn disease (3), sarcoidosis (2), JIA (1), reactive arthritis (1), rheumatoid arthritis (1), relapsing polychondritis (1), TINU (1), pars planitis (1), Birdshot (1) and idiopathic uveitis (3). Uveitis pattern was anterior (n=55), posterior (6), panuveitis (6) and intermediate (4).

Prior to CZP, patients had received: methotrexate (37), sulfasalazine (26), azathioprine (14), cyclosporine (10), leflunomide (3), mycophenolate mofetil (3) and cyclophosphamide (1). Previous BT was administered in 48 (67.6%) patients, with a mean of 1.4±1.3 drugs per patient as follows: ADA (n=56), IFX (27), golimumab (14), tocilizumab (5) and etanercept (3). Pregnancy was the reason for prescribing CZP in 19 patients. CZP was administered in monotherapy (n=39) or combined with conventional immunosuppressants (n=32).

After a mean follow-up of 27.1±21.1 months, most of the ocular variables showed a rapid and significantly improvement ( Table 1 ). A decrease in the median number [IQR] of flares of uveitis before and after CZP, (3 [1-4] vs. 0 [0-1], p<0.001) was observed. CZP was discontinued in 15 patients due to remission (n=2), ocular insufficient response (2) and incomplete response of extraocular manifestations (11). No serious adverse events were reported.


Conclusion: CZP seems to be effective and safe in patients with refractory uveitis due to IMID.


REFERENCES:

[1]Martín-Varillas JL, et al. Ophthalmology 2018; 125:1444-1451. doi: 10.1016/j.ophtha.2018.02.020.

[2]Atienza-Mateo B, et al. Arthritis Rheumatol 2019; 71:2081-2089. doi: 10.1002/art.41026.

[3]Santos-Gómez M, et al. Clin Exp Rheumatol 2016; 34(6 Suppl 102):S34-S40. PMID: 27054359

[4]Vegas-Revenga N, et al. Am J Ophthalmol 2019; 200:85-94. doi: 10.1016/j.ajo.2018.12.019

[5]Calvo-Río V, et al. Clin Exp Rheumatol. 2014; 32 (4 Suppl 84):S54-7. PMID: 25005576

Baseline 1 st week 1 st Month 6 th Month 1 st year 2 nd year
BCVA (mean±SD) 0.68±0.27 0.72±0.27* 0.79±0.25* 0.84±0.24* 0.85±0.25* 0.87±0.22*
Improvement in AC Cells, n (%) Patients with AC cells at baseline (n=48 ) - 21 (43.7) 30 (62.5)* 41 (85.4)* 48 (100)* 48 (100)*
Improvement in Vitritis, n (%) Patients with vitritis at baseline (n=13 ) - 3 (23.1) 8 (61.5)* 11 (84.6)* 13 (100)* 13 (100)*
OCT (µ ) (mean±SD) 292.5±47.7 294±47.4 286.7±41.9* 274.7±38.7* 272.8±38.9* 266.31±36.2*
Choroiditis; affected eyes, n, (%) 3 (4.2) 3 (4.2) 2 (2.8) 2 (2.8) 1 (1.4) 0 (0)
Retinal Vasculitis; affected eyes, n, (%) 2 (2.8) 0 (0) 1 (1.4) 0 (0) 0 (0) 0 (0)

*p<0.001


Disclosure of Interests: None declared


Citation: Ann Rheum Dis, volume 80, supplement 1, year 2021, page 952
Session: Other orphan diseases (POSTERS only)