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Infliximab Versus Adalimumab in the Treatment of Refractory Inflammatory Uveitis: A Multicenter Study From the French Uveitis Network.
Vallet, Hélène; Seve, Pascal; Biard, Lucie; Baptiste Fraison, Jean; Bielefeld, Philip; Perard, Laurent; Bienvenu, Boris; Abad, Sébastien; Rigolet, Aude; Deroux, Alban; Sene, Damien; Perlat, Antoinette; Marie, Isabelle; Feurer, Elodie; Hachulla, Eric; Fain, Olivier; Clavel, Gaëlle; Riviere, Sophie; Bouche, Pierre-Alban; Gueudry, Julie; Pugnet, Gregory; Le Hoang, Phuc; Resche Rigon, Matthieu; Cacoub, Patrice; Bodaghi, Bahram; Saadoun, David.
Afiliação
  • Vallet H; Hôpital Pitié-Salpêtrière, AP-HP, Centre National de Référence Maladies Systémiques et Autoimmunes Rares, and Université Paris VI, Paris, France.
  • Seve P; Hôpital Croix Rousse, Lyon, France.
  • Biard L; Hôpital Saint Louis and Le Centre de Recherche INSERM, Paris Sorbonne Cité, UMR 1153, Paris, France.
  • Baptiste Fraison J; Hôpital Jean Verdier, Bondy, France.
  • Bielefeld P; Centre Hospitalier Universitaire (CHU) de Dijon, Dijon, France.
  • Perard L; Hôpital Edouard Herriot, Lyon, France.
  • Bienvenu B; CHU de Caen, Caen, France.
  • Abad S; Hôpital Avicenne, Bobigny, France.
  • Rigolet A; Hôpital Pitié-Salpêtrière, AP-HP, Centre National de Référence Maladies Systémiques et Autoimmunes Rares, and Université Paris VI, Paris, France.
  • Deroux A; CHU de Grenoble-Hôpital Michallon, Grenoble, France.
  • Sene D; Hôpital Lariboisière, AP-HP, Paris, France.
  • Perlat A; CHU de Rennes, Rennes, France.
  • Marie I; CHU de Rouen, Rouen, France.
  • Feurer E; Hôpital Croix Rousse, Lyon, France.
  • Hachulla E; Eric Hachulla, MD, PhD: Centre Hospitalier Régional Universitaire de Lille, Lille, France.
  • Fain O; Hôpital Saint Antoine, AP-HP, Paris, France.
  • Clavel G; A. Rothschild Foundation, Paris, France.
  • Riviere S; CHU de Montpellier, Montpellier, France.
  • Bouche PA; Hôpital Saint Louis and Le Centre de Recherche INSERM, Paris Sorbonne Cité, UMR 1153, Paris, France.
  • Gueudry J; CHU de Rouen, Rouen, France.
  • Pugnet G; CHU de Toulouse-Hôpital Purpan, INSERM UMR 1027, Toulouse, France.
  • Le Hoang P; Hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Resche Rigon M; Hôpital Saint Louis and Le Centre de Recherche INSERM, Paris Sorbonne Cité, UMR 1153, Paris, France.
  • Cacoub P; Hôpital Pitié-Salpêtrière, AP-HP, Centre National de Référence Maladies Systémiques et Autoimmunes Rares, and Université Paris VI, Paris, France.
  • Bodaghi B; Hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Saadoun D; Hôpital Pitié-Salpêtrière, AP-HP, Centre National de Référence Maladies Systémiques et Autoimmunes Rares, and Université Paris VI, Paris, France.
Arthritis Rheumatol ; 68(6): 1522-30, 2016 06.
Article em En | MEDLINE | ID: mdl-27015607
ABSTRACT

OBJECTIVE:

To analyze the factors associated with response to anti-tumor necrosis factor (anti-TNF) treatment and compare the efficacy and safety of infliximab (IFX) and adalimumab (ADA) in patients with refractory noninfectious uveitis.

METHODS:

This was a multicenter observational study of 160 patients (39% men and 61% women; median age 31 years [interquartile range 21-42]) with uveitis that had been refractory to other therapies, who were treated with anti-TNF (IFX 5 mg/kg at weeks 0, 2, 6, and then every 5-6 weeks [n = 98] or ADA 40 mg every 2 weeks [n = 62]). Factors associated with complete response were assessed by multivariate analysis. Efficacy and safety of IFX versus ADA were compared using a propensity score approach with baseline characteristics taken into account. Subdistribution hazard ratios (SHRs) and 95% confidence intervals (95% CIs) were calculated.

RESULTS:

The main etiologies of uveitis included Behçet's disease (BD) (36%), juvenile idiopathic arthritis (22%), spondyloarthropathy (10%), and sarcoidosis (6%). The overall response rate at 6 and 12 months was 87% (26% with complete response) and 93% (28% with complete response), respectively. The median time to complete response was 2 months. In multivariate analysis, BD and occurrence of >5 uveitis flares before anti-TNF initiation were associated with complete response to anti-TNF (SHR 2.52 [95% CI 1.35-4.71], P = 0.004 and SHR 1.97 [95% CI 1.02-3.84], P = 0.045, respectively). Side effects were reported in 28% of patients, including serious adverse events in 13%. IFX and ADA did not differ significantly in terms of occurrence of complete response (SHR 0.65 [95% CI 0.25-1.71], P = 0.39), serious side effects (SHR 0.22 [95% CI 0.04-1.25], P = 0.089), or event-free survival (SHR 0.55 [95% CI 0.28-1.08], P = 0.083).

CONCLUSION:

Anti-TNF treatment is highly effective in refractory inflammatory uveitis. BD is associated with increased odds of response. IFX and ADA appear to be equivalent in terms of efficacy.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Uveíte / Fator de Necrose Tumoral alfa / Adalimumab / Infliximab / Anti-Inflamatórios Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Arthritis Rheumatol Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Uveíte / Fator de Necrose Tumoral alfa / Adalimumab / Infliximab / Anti-Inflamatórios Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Arthritis Rheumatol Ano de publicação: 2016 Tipo de documento: Article