Your browser doesn't support javascript.
loading
Sustained Remission and Outcomes with Abatacept plus Methotrexate Following Stepwise Dose De-escalation in Patients with Early Rheumatoid Arthritis.
Emery, Paul; Tanaka, Yoshiya; Bykerk, Vivian P; Huizinga, Thomas W J; Citera, Gustavo; Bingham, Clifton O; Banerjee, Subhashis; Soule, Benjamin P; Nys, Marleen; Connolly, Sean E; Lozenski, Karissa L; Zhuo, Joe; Wong, Robert; Huang, Kuan-Hsiang Gary; Fleischmann, Roy.
Afiliación
  • Emery P; Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds and Leeds NIHR Biomedical Research Centre, Leeds, UK. P.Emery@leeds.ac.uk.
  • Tanaka Y; First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
  • Bykerk VP; Department of Rheumatology, Hospital for Special Surgery, New York City, NY, USA.
  • Huizinga TWJ; Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
  • Citera G; Department of Rheumatology, Instituto de Rehabilitación Psicofísca, Buenos Aires, Argentina.
  • Bingham CO; Divisions of Rheumatology and Allergy, Department of Medicine, Johns Hopkins University, Baltimore, MD, USA.
  • Banerjee S; Immunology and Fibrosis/Global Drug Development, Bristol Myers Squibb, Princeton, NJ, USA.
  • Soule BP; Fibrosis Business Development, Bristol Myers Squibb, Princeton, NJ, USA.
  • Nys M; Global Biometrics and Data Science, Bristol Myers Squibb, Braine-l'Alleud, Belgium.
  • Connolly SE; Immunology and Fibrosis/Global Drug Development, Bristol Myers Squibb, Princeton, NJ, USA.
  • Lozenski KL; Immunology and Fibrosis/Global Drug Development, Bristol Myers Squibb, Princeton, NJ, USA.
  • Zhuo J; Worldwide Health Economics and Outcomes Research, Bristol Myers Squibb, Princeton, NJ, USA.
  • Wong R; Immunology and Fibrosis/Global Drug Development, Bristol Myers Squibb, Princeton, NJ, USA.
  • Huang KG; Immunology and Fibrosis/Global Drug Development, Bristol Myers Squibb, Princeton, NJ, USA.
  • Fleischmann R; Division of Rheumatology, University of Texas Southwestern Medical Center and Metroplex Clinical Research Center, Dallas, TX, USA.
Rheumatol Ther ; 10(3): 707-727, 2023 Jun.
Article en En | MEDLINE | ID: mdl-36869251
Patients with rheumatoid arthritis (RA) experience inflamed and damaged joints. RA is an autoimmune disease in which proteins called autoantibodies, particularly anti-citrullinated protein autoantibodies, target the patient's own joint tissue and organs by mistake, leading to symptomatic inflammation. Successful treatment can decrease the disease's activity to a state known as remission. Patients in remission may experience little or no symptoms and it may be possible for some to then be able to decrease their treatment. Here, we report the results of a large, international study that looked at two treatments, abatacept and methotrexate, in patients with RA and anti-citrullinated protein autoantibodies. The study had two parts. Firstly, to see how many patients had success (remission) with weekly abatacept and/or methotrexate treatment, and secondly, to see if remission was maintained when treatment was either continued or decreased and stopped. The study showed that the number of patients in remission 6 months after treatment started was not greatly different between patients treated with both abatacept and methotrexate and those treated with just methotrexate. Those taking abatacept and methotrexate together had better remission rates 1 year later. More patients also stayed in remission when they continued to receive both abatacept and methotrexate compared with those who were just treated with abatacept or when their abatacept treatment was decreased and stopped. More patients stayed in remission when abatacept was decreased than when it was stopped. The results from this study may help determine possible future treatment reduction and/or withdrawal plans for some patients with RA.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Rheumatol Ther Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Rheumatol Ther Año: 2023 Tipo del documento: Article