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Safety of Roxadustat Versus Erythropoiesis-Stimulating Agents in Patients with Anemia of Non-dialysis-Dependent or Incident-to-Dialysis Chronic Kidney Disease: Pooled Analysis of Four Phase 3 Studies.
Barratt, Jonathan; Dellanna, Frank; Portoles, Jose; Choukroun, Gabriel; De Nicola, Luca; Young, James; Dimkovic, Nada; Reusch, Michael.
Afiliação
  • Barratt J; Department of Cardiovascular Sciences, University of Leicester, University Rd, Leicester, LE1 7RH, UK. jb81@le.ac.uk.
  • Dellanna F; Department of Nephrology and Dialysis, MVZ DaVita Rhein-Ruhr GmbH, Düsseldorf, Germany.
  • Portoles J; Department of Nephrology, Hospital Universitario Puerta de Hierro, Madrid, Spain.
  • Choukroun G; Department of Nephrology, Anemia Working Group Spanish Society of Nephrology, Madrid, Spain.
  • De Nicola L; Department of Nephrology, Dialysis and Transplantation, CHU Amiens Picardie and Jules Verne University, Amiens, France.
  • Young J; Department of Nephrology, University of Campania, Naples, Italy.
  • Dimkovic N; Department of Statistics, Astellas Pharma, Inc., Northbrook, IL, USA.
  • Reusch M; Department of Internal Medicine, University of Belgrade, Belgrade, Serbia.
Adv Ther ; 40(4): 1546-1559, 2023 04.
Article em En | MEDLINE | ID: mdl-36749544
INTRODUCTION: This study was conducted to elucidate the safety of roxadustat, an oral medication, in patients with non-dialysis-dependent (NDD) or incident dialysis dialysis-dependent (ID-DD) chronic kidney disease (CKD). METHODS: Safety results from four phase 3, randomized, open-label studies comparing roxadustat to an erythropoiesis-stimulating agent (ESA) in men and women with NDD or ID-DD CKD with anemia were pooled and evaluated. Endpoints were time to major adverse cardiovascular event (MACE; myocardial infarction, stroke, and all-cause mortality) and MACE+ (MACE plus congestive heart failure or unstable angina requiring hospitalization), all-cause mortality, and treatment-emergent adverse events (TEAEs). MACE and MACE+ were evaluated for non-inferiority at 1.8- and 1.3-margins using hazard ratios (HRs) and 95% confidence intervals (CIs). TEAEs were descriptively summarized. RESULTS: In total, 2142 patients were evaluated (1083 roxadustat; 1059 ESA). Roxadustat was comparable to ESA for risk of MACE (HR 0.79, 95% CI 0.61-1.02), MACE+ (HR 0.78, 95% CI 0.62-0.98), and all-cause mortality (HR 0.78, 95% CI 0.57-1.05). TEAEs were comparable between roxadustat and ESA groups, including any TEAE [incidence rate per 100 (IR/100) patient-exposure years 56.1 vs. 53.5], TEAEs leading to study drug discontinuation (IR/100 patient-exposure years 6.7 vs. 5.1), and TEAEs leading to death (IR/100 patient-exposure years 6.9 vs. 7.4). CONCLUSION: There was no evidence of increased risk of cardiovascular events or mortality with roxadustat compared with ESA in patients with anemia who have NDD or ID-DD CKD. Although TEAEs occurred commonly in both the roxadustat and ESA groups, patients infrequently discontinued the study drug because of an adverse event. CLINICAL TRIAL REGISTRATION NUMBERS: DOLOMITES, 1517-CL-0610 [NCT02021318]; HIMALAYAS, FGCL-4592-063 [NCT02052310]; SIERRAS, FGCL-4592-064 [NCT02273726]; and ROCKIES, D5740C00002 [NCT02174731].
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica / Hematínicos / Anemia Tipo de estudo: Clinical_trials / Etiology_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica / Hematínicos / Anemia Tipo de estudo: Clinical_trials / Etiology_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article