Efficacy and safety of vadadustat compared to darbepoetin alfa on anemia in patients with chronic kidney disease: a meta-analysis.

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  • Author(s): Huang Q;Huang Q; Liao Z; Liao Z; Liu X; Liu X; Xia Y; Xia Y; Wang J; Wang J
  • Source:
    International urology and nephrology [Int Urol Nephrol] 2023 Feb; Vol. 55 (2), pp. 325-334. Date of Electronic Publication: 2022 Aug 12.
  • Publication Type:
    Meta-Analysis; Journal Article; Review
  • Language:
    English
  • Additional Information
    • Source:
      Publisher: Springer Country of Publication: Netherlands NLM ID: 0262521 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-2584 (Electronic) Linking ISSN: 03011623 NLM ISO Abbreviation: Int Urol Nephrol Subsets: MEDLINE
    • Publication Information:
      Publication: Amsterdam : Springer
      Original Publication: Budapest, Akademiai Kiadó
    • Subject Terms:
    • Abstract:
      Objective: As a novel oral agent in treating anemia of chronic kidney disease (CKD), several clinical trials of vadadustat have been conducted to compare with darbepoetin alfa. This study systematically reviews and investigates the efficacy and safety of vadadustat in the anemia treatment with different duration in both nondialysis-dependent CKD (NDD-CKD) and dialysis-dependent CKD (DD-CKD).
      Methods: Several main databases were searched for randomized controlled trials (RCTs) reporting vadadustat vs darbepoetin alfa for anemia patients with CKD. The outcome indicators were focused on hemoglobin (Hb), the percentage of patients within the target Hb, the need for RBC (Red Blood Cell) transfusions, and serious adverse events (SAEs).
      Results: Four eligible studies with 8,026 participants were included. The changes of Hb levels from the baseline in the darbepoetin alfa group were significantly higher than that in the vadadustat group with DD-CKD (mean difference (MD) - 0.19, [95% confidence interval (CI), - 0.21 to - 0.17], p < 0.0001). In NDD-CKD patients, the changes of Hb levels in the two groups are not significantly different (MD = - 0.06, [95% CI, - 0.18 to 0.05], p = 0.006), especially, during the treatment duration of 20-36 weeks (MD = 0.02, [95% CI, - 0.04 to 0.08], p = 0.51). The percentage of patients within the target Hb was significantly lower in the vadadustat group than that in the darbepoetin alfa group in DD-CKD patients (MD = 0.9, [95% CI, 0.86 to 0.94], p < 0.00001), while in NDD-CKD patients, there was no significant difference (MD = 1.05, [95% CI, 0.99 to 1.12], p < 0.00001). In terms of safety, the two agents had no significant difference in the incidence of RBC transfusions and SAEs (RR = 1.26 [95% CI, 0.99 to 1.61], p = 0.52; RR = 0.97, [95% CI, 0.94 to 1.01], p = 0.19; respectively).
      Conclusion: Compared to darbepoetin alfa, vadadustat had the same effect in raising the hemoglobin level in NDD-CKD patients in the short term. Vadadustat may become an effective and safe alternative for the treatment of patients with anemia and CKD, especially in NDD-CKD patients. As the application of vadadustat is still under exploration, future research should compensate for the limitations of our study to estimate the vadadustat's value.
      (© 2022. The Author(s), under exclusive licence to Springer Nature B.V.)
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    • Grant Information:
      JCYJ201803021537014062 Shenzhen Science and Technology Innovation Commission of China
    • Contributed Indexing:
      Keywords: Anemia; Chronic kidney disease; Darbepoetin alfa; Meta-analysis; Vadadustat
    • Accession Number:
      15UQ94PT4P (Darbepoetin alfa)
      0 (vadadustat)
      11096-26-7 (Erythropoietin)
      0 (Hematinics)
      0 (Hemoglobins)
    • Publication Date:
      Date Created: 20220812 Date Completed: 20230124 Latest Revision: 20230201
    • Publication Date:
      20240829
    • Accession Number:
      10.1007/s11255-022-03316-z
    • Accession Number:
      35960479