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Sustained glucocorticoid tapering in the phase 3 trials of anifrolumab: a post hoc analysis of the TULIP-1 and TULIP-2 trials.
Bruce, Ian N; van Vollenhoven, Ronald F; Morand, Eric F; Furie, Richard A; Manzi, Susan; White, William B; Abreu, Gabriel; Tummala, Raj.
Afiliación
  • Bruce IN; Centre for Epidemiology Versus Arthritis, The University of Manchester and NIHR Manchester Biomedical Research Centre, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.
  • van Vollenhoven RF; Amsterdam Rheumatology and Immunology Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Morand EF; School of Clinical Sciences at Monash Health, Monash University, Melbourne, VIC, Australia.
  • Furie RA; Division of Rheumatology, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Great Neck, NY, USA.
  • Manzi S; Lupus Center of Excellence, Autoimmunity Institute, Allegheny Health Network, Pittsburgh, PA, USA.
  • White WB; Calhoun Cardiology Center, University of Connecticut School of Medicine, Farmington, CT, USA.
  • Abreu G; BioPharmaceuticals R&D, AstraZeneca R&D, Gothenburg, Sweden.
  • Tummala R; BioPharmaceuticals R&D, AstraZeneca US, Gaithersburg, MD, USA.
Rheumatology (Oxford) ; 62(4): 1526-1534, 2023 04 03.
Article en En | MEDLINE | ID: mdl-36018235
OBJECTIVES: Glucocorticoid sparing is a key priority for SLE management. We evaluated the effects of sustained glucocorticoid tapering in patients with SLE. MATERIAL AND METHODS: This was a post hoc analysis of the randomized, placebo-controlled, 52-week phase 3 Treatment of Uncontrolled Lupus via the Interferon Pathway (TULIP)-1 and TULIP-2 trials of anifrolumab (300 mg i.v. once every 4 weeks for 48 weeks) plus standard therapy in patients with moderate to severe SLE. In a cohort of patients receiving glucocorticoids (prednisone or equivalent) 10 mg or more per day at baseline, we assessed changes in glucocorticoid dosage, patient-reported outcomes (PROs) and safety. Outcome measures were compared between sustained glucocorticoid taper responders (7.5 mg or less per day by week 40 sustained through week 52) and non-responders, regardless of treatment group, and between patients receiving anifrolumab or placebo. RESULTS: Among the 726 patients in the TULIP trials, 375 patients received glucocorticoids 10 mg or more per day at baseline, and of these, 155 (41%) patients were sustained glucocorticoid taper responders. Compared with non-responders (n = 220), sustained glucocorticoid taper responders reduced their mean cumulative glucocorticoid dose by 32%, improved PRO scores, reduced blood pressure and experienced fewer serious adverse events. Sustained glucocorticoid tapering was achieved by 51% (96/190) of patients receiving anifrolumab vs 32% (59/185) receiving placebo. Compared with placebo, more anifrolumab-treated patients achieved both sustained glucocorticoid taper and reduced overall disease activity [38% (72/190) vs 23% (43/185)]. CONCLUSIONS: Sustained glucocorticoid tapering is associated with clinical benefits. Anifrolumab treatment has potential to reduce disease activity and glucocorticoid exposure, a key goal of SLE management. STUDY REGISTRATION: ClinicalTrials.gov identifier: NCT02446912 and NCT02446899.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tulipa / Lupus Eritematoso Sistémico Tipo de estudio: Clinical_trials / Prognostic_studies Aspecto: Patient_preference Límite: Humans Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tulipa / Lupus Eritematoso Sistémico Tipo de estudio: Clinical_trials / Prognostic_studies Aspecto: Patient_preference Límite: Humans Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido