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Towards a novel clinical outcome assessment for systemic lupus erythematosus: first outcomes of an international taskforce.
Connelly, Kathryn; Eades, Laura E; Koelmeyer, Rachel; Ayton, Darshini; Golder, Vera; Kandane-Rathnayake, Rangi; Gregory, Kate; Brunner, Hermine; Burke, Laurie; Arnaud, Laurent; Askanase, Anca; Aranow, Cynthia; Vital, Ed; Pons-Estel, Guillermo; Dantata, Khadija; Andersen, Jeanette; Cornet, Alain; Buie, Joy; Sun, Ying; Tanaka, Yoshiya; Simon, Lee; Lahoud, Youmna; Friedman, Alan; Kalunian, Kenneth; Zuraw, Qing; Werth, Victoria; Garces, Sandra; Morand, Eric F.
Afiliação
  • Connelly K; School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia. kathryn.connelly@monash.edu.
  • Eades LE; School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia.
  • Koelmeyer R; School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia.
  • Ayton D; School of Public Health and Preventive Medicine, Monash University, Clayton, Victoria, Australia.
  • Golder V; School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia.
  • Kandane-Rathnayake R; School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia.
  • Gregory K; School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia.
  • Brunner H; Division of Rheumatology, Cincinnati Children's Hospital, University of Cincinnati, Cincinatti, OH, USA.
  • Burke L; LORA Group, Royal Oak, MI, USA.
  • Arnaud L; Department of Rheumatology, National Reference Center for Autoimmune Diseases (RESO), Hopitaux Universitaires de Strasbourg, Strasbourg, Alsace, France.
  • Askanase A; Lupus Center, Columbia University Medical Center, New York City, NY, USA.
  • Aranow C; Lupus Centre of Excellence, Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY, USA.
  • Vital E; Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK.
  • Pons-Estel G; NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Dantata K; Departamento de Medicina Interna, Centro Regional de Enfermedades Autoinmunes y Reumáticas de Grupo Oroño (GO CREAR), Rosario, Argentina.
  • Andersen J; Lupus Foundation of America, Washington, DC, USA.
  • Cornet A; Lupus Europe, Brussels, Belgium.
  • Buie J; Lupus Europe, Brussels, Belgium.
  • Sun Y; Lupus Foundation of America, Washington, DC, USA.
  • Tanaka Y; Merck Healthcare KGaA, Darmstadt, Hesse, Germany.
  • Simon L; The First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Fukuoka, Japan.
  • Lahoud Y; SDG LLC, Cambridge, MA, USA.
  • Friedman A; Biogen, Cambridge, MA, USA.
  • Kalunian K; AbbVie, Libertyville, IL, USA.
  • Zuraw Q; Division of Rheumatology, Allergy and Immunology, University of California, San Diego, CA, USA.
  • Werth V; Janssen Research and Development, Spring House, PA, USA.
  • Garces S; Department of Dermatology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
  • Morand EF; Amgen, Thousand Oaks, CA, USA.
Nat Rev Rheumatol ; 19(9): 592-602, 2023 09.
Article em En | MEDLINE | ID: mdl-37433880
Systemic lupus erythematosus (SLE) is a disease of high unmet therapeutic need. The challenge of accurately measuring clinically meaningful responses to treatment has hindered progress towards positive outcomes in SLE trials, impeding the approval of potential new therapies. Current primary end points used in SLE trials are based on legacy disease activity measures that were neither specifically designed for the clinical trial context, nor developed according to contemporary recommendations for clinical outcome assessments (COAs), such as that substantial patient input should be incorporated into their design. The Treatment Response Measure for SLE (TRM-SLE) Taskforce is a global collaboration of SLE clinician-academics, patients and patient representatives, industry partners and regulatory experts, established to realize the goal of developing a new COA for SLE clinical trials. The aim of this project is a novel COA designed specifically to measure treatment effects that are clinically meaningful to patients and clinicians, and intended for implementation in a trial end point that supports regulatory approval of novel therapeutic agents in SLE. This Consensus Statement reports the first outcomes of the TRM-SLE project, including a structured process for TRM-SLE development.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lúpus Eritematoso Sistêmico Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lúpus Eritematoso Sistêmico Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article