Artículos de revistas
Long-Term Safety and Efficacy of Abatacept in Children With Juvenile Idiopathic Arthritis
Fecha
2010-06-01Registro en:
Arthritis and Rheumatism. Hoboken: Wiley-liss, v. 62, n. 6, p. 1792-1802, 2010.
0004-3591
10.1002/art.27431
WOS:000279432500031
7098310008371632
0000-0002-7631-7093
Autor
Univ Genoa
Cincinnati Childrens Hosp Med Ctr
Hop Necker Enfants Malad
Inst Salud Nino
Hosp Univ Dr JE Gonzalez
Hosp Das Clin
Hosp Cent Dr Ignacio Morones Prieto
Univ Nacl Autonoma Mexico
Hosp Gen Mexico City
Ist Gaetano Pini
Inst Portugues Reumatol
Universidade Estadual Paulista (Unesp)
Hosp Nacl Edgardo Rebagliati
Landeskrankenhaus Bregenz
Altoona Arthrit & Osteoporosis Ctr
Hosp Univ A Coruna
Hamburger Zentrum Kinder & Jugendrheumatol
Ctr Multisite Romand Rhumatol Pediat
Zentrum Allgemeine Paediat & Nenatol
Prof Hess Kinderklin
Hop St Vincent de Paul
Charite
Texas Scottish Rite Hosp Crippled Children
Hosp Nino Poblano
Bristol Myers Squibb
Institución
Resumen
Objective. We previously documented that abatacept was effective and safe in patients with juvenile idiopathic arthritis (JIA) who had not previously achieved a satisfactory clinical response with disease-modifying antirheumatic drugs or tumor necrosis factor blockade. Here, we report results from the long-term extension (LTE) phase of that study.Methods. This report describes the long-term, open-label extension phase of a double-blind, randomized, controlled withdrawal trial in 190 patients with JIA ages 6-17 years. Children were treated with 10 mg/kg abatacept administered intravenously every 4 weeks, with or without methotrexate. Efficacy results were based on data derived from the 153 patients who entered the open-label LTE phase and reflect >= 21 months (589 days) of treatment. Safety results include all available open-label data as of May 7, 2008.Results. of the 190 enrolled patients, 153 entered the LTE. By day 589, 90%, 88%, 75%, 57%, and 39% of patients treated with abatacept during the double-blind and LTE phases achieved responses according to the American College of Rheumatology (ACR) Pediatric 30 (Pedi 30), Pedi 50, Pedi 70, Pedi 90, and Pedi 100 criteria for improvement, respectively. Similar response rates were observed by day 589 among patients previously treated with placebo. Among patients who had not achieved an ACR Pedi 30 response at the end of the open-label lead-in phase and who proceeded directly into the LTE, 73%, 64%, 46%, 18%, and 5% achieved ACR Pedi 30, Pedi 50, Pedi 70, Pedi 90, and Pedi 100 responses, respectively, by day 589 of the LTE. No cases of tuberculosis and no malignancies were reported during the LTE. Pneumonia developed in 3 patients, and multiple sclerosis developed in 1 patient.Conclusion. Abatacept provided clinically significant and durable efficacy in patients with JIA, including those who did not initially achieve an ACR Pedi 30 response during the initial 4-month open-label lead-in phase.