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. 2022 Dec 6;8(2):e002693. doi: 10.1136/rmdopen-2022-002693

Table 2.

Treatment schedule and long-term follow-up of a series of 80 patients with refractory uveitis due to immune-mediated inflammatory diseases (IMID) treated with certolizumab pegol (CZP)

Conventional immunosuppressant before CZP initiation, n (%) 60 (75)
 Ciclosporin 10 (12.5)
 Azathioprine 14 (17.5)
 Methotrexate 38 (47.5)
 Salazopyrin 28 (35.0)
 Cyclophosphamide 1 (1.3)
 Mycophenolate 4 (5.0)
 Leflunomide 3 (3.8)
 Pulses of intravenous MP 4 (5.0)
Biological treatment before CZP initiation, n (%) 52 (63)
 No. of biological drugs per patient, median (IQR) 2(1–3)
 Adalimumab 48 (60)
 Infliximab 32 (40)
 Etanercept 7 (8.8)
 Golimumab 15 (18.8)
 Tocilizumab 5 (6.3)
 Rituximab 1 (1.3)
 Secukinumab 1 (1.3)
 Gevokizumab 1 (1.3)
Mean dose of prednisone at CZP initiation (mg/day), mean±SD 16.9±10.8
CZP regimen
 Monotherapy/Combination, n (%) 39/41 (48.8/51.2)
 Ciclosporin 1 (1.3)
 Azathioprine 9 (11.3)
 Methotrexate 23 (28.8)
 Salazopyrine 7 (8.8)
 Hydroxychloroquine 1 (1.3)
Follow-up time since CZP initiation (months), median (IQR) 24 (12–36)
 Optimisation, n (%) 12 (15)
 Reason for withdrawal, n (%) 16 (20)
  Remission 3 (3.8)
  Ocular inefficacy 4 (5)
  Extraocular inefficacy 9 (11.3)
  Side effects 0 (0.0)

MP, methylprednisolone.