Alicia Marquet1,2, Catherine Chapelon-Abric3, Delphine Maucort-Boulch4,5, Fleur Cohen-Aubart6, Laurent Pérard2,7, Laurence Bouillet8, Sébastien Abad9, Philip Bielefeld10, Diane Bouvry11, Marc André12, Nicolas Noël13, Boris Bienvenu14, Alice Proux15, Sandra Vukusic2,16, Bahram Bodaghi17, Françoise Sarrot-Reynaud8, Jean Iwaz4,5, Christiane Broussolle1,2, David Saadoun3, Yvan Jamilloux1,2, Dominique Valeyre11, Pascal Sève1,2. 1. Département de Médecine Interne, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, F-69004, Lyon, France. 2. Université Claude Bernard, Lyon 1, F-69100, Villeurbanne, France. 3. Département de Médecine Interne et d'Immunologie Clinique II, Assistance Publique-Hôpitaux de Paris (AP-HP), CHU Pitié Salpêtrière, Université Pierre et Marie Curie (UPMC), F-75006, Paris, France. 4. Service de Biostatistique, Hospices Civils de Lyon, F-69003, Lyon, France. 5. CNRS UMR 5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique-Santé, F-69100, Villeurbanne, France. 6. Département de Médecine Interne et d'Immunologie Clinique, AP-HP, CHU Pitié Salpêtrière, Institut E3M, Université Pierre et Marie Curie, F-75006, Paris, France. 7. Département de Médecine Interne, Hôpital Edouard Herriot, Hospices Civils de Lyon, F-69003 Lyon, France. 8. Département de Médecine Interne, Centre Hospitalier Universitaire, F-38700, Grenoble, France. 9. Département de Médecine Interne, Hôpital Avicenne, Université Paris 13, F-93000, Bobigny, France. 10. Département de Médecine Interne, Centre Hospitalier Universitaire, F-21000, Dijon, France. 11. Département de Pneumologie, Hôpital Avicenne, AP-HP, Université Paris 13, F-93000, Bobigny, France. 12. Département de Médecine Interne, CHU Gabriel Montpied, F-63000, Clermont-Ferrand, France. 13. Département de Médecine Interne et d'Immunologie Clinique, AP-HP, CHU Bicêtre, Université Paris Sud, UMR 1184, F-94270, Le Kremlin Bicêtre, France. 14. Département de Médecine Interne, Centre Hospitalier Universitaire, F-14033, Caen, France. 15. Département de Médecine Interne de Gériatrie Thérapeutique, Hôpital Saint-Julien, CHU de Rouen, F-76031 Rouen Cedex, France. 16. Département de Neurologie, Hospices Civils de Lyon, F-69500, Bron, France. 17. Département d'Ophtalmologie, AP-HP, CHU Pitié Salpêtrière, F-75013, Paris, France.
Abstract
Backgroung: This study investigated the efficacy and safety of TNF antagonists in sarcoid uveitis in unselected cases. Design: This is a multicentre study on patients with sarcoidosis who received TNF antagonists in pneumology and internal medicine departments in France. We present here the subgroup of patients with biopsy-proven sarcoid uveitis included in the nationwide registry STAT (Sarcoidosis treated with TNF AnTagonists). Results: Among the 132 patients included in this multicenter study, 18 patients with refractory uveitis were treated as a first-line TNF antagonist with infliximab (n=14), adalimumab (n=3) and certolizumab (n=1). Before anti-TNF initiation, the median duration of sarcoidosis was 42 months and 83% of the patients have been treated with at least one immunosuppressive drug. Six patients switched for a second-line TNF antagonist. After a mean time under treatment of 29 months, the treatment resulted in a significant decrease of the ophthalmic extrapulmonary Physician Organ Severity Tool (ePOST) (mean score: 4.2 vs. 2.6) scores and a steroid sparing effect (29.4±20.7 vs. 6.2±5.2 mg/d). Overall, the ophthalmic response, either complete or partial, was 67%. Nine patients (50%) presented adverse events, including severe infectious complications in 5 patients, which required anti-TNF treatment interruption in 6 cases (33%). Among the 7 responder patients who discontinued anti-TNF therapy, 71% relapsed. Finally, 12 patients (67%) could continue TNF antagonist treatment. Conclusions: TNF antagonists were efficient in 67% of biopsy-proven refractory sarcoid uveitis. Severe adverse events, mainly infectious complications, were frequent. The high frequency of relapses after anti-TNF-α discontinuation requires a close patient follow-up thereafter. (Sarcoidosis Vasc Diffuse Lung Dis 2017; 34: 74-80). Copyright:
Backgroung: This study investigated the efficacy and safety of TNF antagonists in sarcoid uveitis in unselected cases. Design: This is a multicentre study on patients with sarcoidosis who received TNF antagonists in pneumology and internal medicine departments in France. We present here the subgroup of patients with biopsy-proven sarcoid uveitis included in the nationwide registry STAT (Sarcoidosis treated with TNF AnTagonists). Results: Among the 132 patients included in this multicenter study, 18 patients with refractory uveitis were treated as a first-line TNF antagonist with infliximab (n=14), adalimumab (n=3) and certolizumab (n=1). Before anti-TNF initiation, the median duration of sarcoidosis was 42 months and 83% of the patients have been treated with at least one immunosuppressive drug. Six patients switched for a second-line TNF antagonist. After a mean time under treatment of 29 months, the treatment resulted in a significant decrease of the ophthalmic extrapulmonary Physician Organ Severity Tool (ePOST) (mean score: 4.2 vs. 2.6) scores and a steroid sparing effect (29.4±20.7 vs. 6.2±5.2 mg/d). Overall, the ophthalmic response, either complete or partial, was 67%. Nine patients (50%) presented adverse events, including severe infectious complications in 5 patients, which required anti-TNF treatment interruption in 6 cases (33%). Among the 7 responder patients who discontinued anti-TNF therapy, 71% relapsed. Finally, 12 patients (67%) could continue TNF antagonist treatment. Conclusions: TNF antagonists were efficient in 67% of biopsy-proven refractory sarcoid uveitis. Severe adverse events, mainly infectious complications, were frequent. The high frequency of relapses after anti-TNF-α discontinuation requires a close patient follow-up thereafter. (Sarcoidosis Vasc Diffuse Lung Dis 2017; 34: 74-80). Copyright:
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