Comparative efficacy between adalimumab and infliximab in the treatment of non-infectious intermediate uveitis, posterior uveitis, and panuveitis: a retrospective observational study of 107 patients

被引:0
作者
Claudia Fabiani
Antonio Vitale
Donato Rigante
Giacomo Emmi
Alice Bitossi
Giuseppe Lopalco
Jurgen Sota
Silvana Guerriero
Ida Orlando
Stefano Gentileschi
Florenzo Iannone
Bruno Frediani
Mauro Galeazzi
Lorenzo Vannozzi
Gian Marco Tosi
Luca Cantarini
机构
[1] University of Siena,Ophthalmology Unit, Department of Medicine, Surgery and Neuroscience
[2] University of Siena,Research Center of Systemic Autoinflammatory Diseases and Behçet’s Disease and Rheumatology
[3] Università Cattolica Sacro Cuore,Ophthalmology Collaborative Uveitis Center, Department of Medical Sciences, Surgery and Neurosciences
[4] Fondazione Policlinico Universitario A. Gemelli I.R.C.C.S,Institute of Pediatrics
[5] University of Florence,Department of Experimental and Clinical Medicine
[6] University of Florence,Department of Surgery and Translational Medicine, Eye Clinic
[7] University of Bari,Interdisciplinary Department of Medicine, Rheumatology Unit
[8] University of Bari,Department of Ophthalmology and Otolaryngology
来源
Clinical Rheumatology | 2019年 / 38卷
关键词
Behçet’s disease; Macular edema; Retinal vasculitis; TNF-blocking antibodies; Uveitis;
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学科分类号
摘要
To compare the efficacy of adalimumab (ADA) and infliximab (IFX) in patients with non-infectious intermediate uveitis, posterior uveitis, and panuveitis. Demographic, clinical, instrumental, and therapeutic data from patients enrolled were collected at the start of treatment, at 12-month follow-up, and at the last follow-up assessment. One hundred seven patients (46 females, 187 eyes) were enrolled, 66 (61.7%) treated with ADA and 41 (38.3%) with IFX. Bilateral involvement was observed in 80 cases. The mean follow-up was 26.45 ± 21.71 months for ADA patients and 56.60 ± 56.04 months for IFX patients. The overall decrease of uveitis frequency during the first 12 months of treatment was 66.7% in the IFX group and 84.2% in the ADA group, compared to the previous 12 months (p = 0.09). A significantly higher corticosteroid dosage was found among patients treated with ADA at the last follow-up visit (p = 0.008). The percentage of patients co-administered with corticosteroids was significantly higher among ADA patients both at the 12-month visit (p = 0.03) and at the last visit (p = 0.0004). The frequency of uveitic macular edema (UME) was significantly higher among patients treated with ADA compared to those treated with IFX at the 12-month assessment (p = 0.015) and at the last follow-up visit (p = 0.011); central macular thickness was significantly higher in ADA group compared to the IFX group at the last follow-up assessment (p = 0.04). ADA and IFX have shown a similar efficacy in controlling uveitis relapses, but IFX showed a more pronounced corticosteroid sparing effect and a significantly higher capacity in resolving UME compared to ADA.
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页码:407 / 415
页数:8
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