4.6 Article Retracted Publication

被撤回的出版物: Pooled Analysis of Roxadustat for Anemia in Patients With Kidney Failure Incident to Dialysis (Retracted article. See vol. 7, pg. 665, 2022)

Journal

KIDNEY INTERNATIONAL REPORTS
Volume 6, Issue 3, Pages 613-623

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ekir.2020.12.018

Keywords

anemia; chronic kidney disease; dialysis; roxadustat

Funding

  1. FibroGen, Inc.
  2. AstraZeneca

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The study showed that roxadustat was at least as effective as epoetin alfa in patients new to dialysis, with a lower risk of major adverse cardiovascular events and MACE+ in the roxadustat group compared to the epoetin alfa group.
Introduction: Erythropoiesis-stimulating agents are associated with increased cardiovascular risk when higher doses are used toward higher hematocrit targets. Patients new to dialysis are at higher risk for morbidity and mortality. Systematic evaluation of this population was predefined in the roxadustat clinical development program. Roxadustat is a hypoxia-inducible prolyl hydroxylase inhibitor. Methods: Data were pooled from 3 phase 3, randomized, open-label, active-controlled trials. Eligible adults had kidney failure and initiated dialysis for 2 weeks to <= 4 months prior to randomization to roxadustat or epoetin alfa. Efficacy was assessed as mean change in hemoglobin from baseline averaged over weeks 28 to 52, regardless of rescue therapy. Key cardiovascular safety endpoints were major adverse cardiovascular events (MACE; all-cause mortality [ACM], myocardial infarction, and stroke), and MACE+ (MACE plus unstable angina or congestive heart failure requiring hospitalization), and ACM. Results: This study included 1530 patients with kidney failure incident to dialysis. Mean (SD) changes in hemoglobin from baseline averaged over weeks 28 to 52, regardless of rescue therapy, were 2.12 (1.45) versus 1.91 (1.42) g/dl in the roxadustat and epoetin alfa groups (least-squares mean difference: 0.22; 95% CI, 0.05 to 0.40; P 1/4 0.0130). Risks of MACE and MACE+ were lower in the roxadustat group (hazard ratio [HR], 0.70; 95% CI, 0.51 to 0.96) than the epoetin alfa group (HR, 0.66; 95% CI, 0.50 to 0.89); the HR for ACM was 0.76 (95% CI, 0.52 to 1.11). Conclusion: Roxadustat was at least as efficacious as epoetin alfa. Roxadustat had a lower risk of MACE/ MACE+ in patients new to dialysis.

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