dc.contributorUniv Genoa
dc.contributorCincinnati Childrens Hosp Med Ctr
dc.contributorHop Necker Enfants Malad
dc.contributorInst Salud Nino
dc.contributorHosp Univ Dr JE Gonzalez
dc.contributorHosp Das Clin
dc.contributorHosp Cent Dr Ignacio Morones Prieto
dc.contributorUniv Nacl Autonoma Mexico
dc.contributorHosp Gen Mexico City
dc.contributorIst Gaetano Pini
dc.contributorInst Portugues Reumatol
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorHosp Nacl Edgardo Rebagliati
dc.contributorLandeskrankenhaus Bregenz
dc.contributorAltoona Arthrit & Osteoporosis Ctr
dc.contributorHosp Univ A Coruna
dc.contributorHamburger Zentrum Kinder & Jugendrheumatol
dc.contributorCtr Multisite Romand Rhumatol Pediat
dc.contributorZentrum Allgemeine Paediat & Nenatol
dc.contributorProf Hess Kinderklin
dc.contributorHop St Vincent de Paul
dc.contributorCharite
dc.contributorTexas Scottish Rite Hosp Crippled Children
dc.contributorHosp Nino Poblano
dc.contributorBristol Myers Squibb
dc.date.accessioned2014-05-20T13:38:03Z
dc.date.available2014-05-20T13:38:03Z
dc.date.created2014-05-20T13:38:03Z
dc.date.issued2010-06-01
dc.identifierArthritis and Rheumatism. Hoboken: Wiley-liss, v. 62, n. 6, p. 1792-1802, 2010.
dc.identifier0004-3591
dc.identifierhttp://hdl.handle.net/11449/13201
dc.identifier10.1002/art.27431
dc.identifierWOS:000279432500031
dc.identifier7098310008371632
dc.identifier0000-0002-7631-7093
dc.description.abstractObjective. 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.
dc.languageeng
dc.publisherWiley-liss
dc.relationArthritis and Rheumatism
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.titleLong-Term Safety and Efficacy of Abatacept in Children With Juvenile Idiopathic Arthritis
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución