Iron chelation of hetrombopag in aplastic anemia: a post hoc analysis of a phase II study

Ann Hematol. 2022 Dec;101(12):2611-2616. doi: 10.1007/s00277-022-04968-8. Epub 2022 Oct 11.

Abstract

Hetrombopag is the only CFDA-approved thrombopoietin (TPO) receptor agonist for severe aplastic anemia (SAA) in China. Its chemical structure has an iron chelation domain. To explore the iron chelation effect of hetrombopag, we performed a post hoc analysis of the phase II clinical trial (NCT03557099). Thirty-five immunosuppressive therapy (IST)-refractory SAA patients were enrolled in the study, and the longitudinal changes of serum ferritin (SF) were assessed. At 18 weeks post-hetrombopag initiation, 51.4% of patients showed decreased SF levels by a median of 49.0 (18.1-95.5) % from baseline (median ΔSF decrease value, 917.2 ng/ml, range from 104.0 to 7030.0 ng/ml). A decrease in SF was found in 75.0% of hematologic responders and 31.6% of non-responders. Among the 24 patients with iron overload, 12 had decreased SF levels by up to 51% of the baseline. Patients with normal SF levels also showed decreased SF levels, and iron deficiency occurred in two patients. In conclusion, hetrombopag showed a powerful and rapid iron chelation effect.

Keywords: Aplastic anemia; Hetrombopag; Iron chelation.

Publication types

  • Clinical Trial, Phase II

MeSH terms

  • Anemia, Aplastic* / drug therapy
  • Humans
  • Hydrazones / therapeutic use
  • Iron Chelating Agents / therapeutic use
  • Pyrazolones* / therapeutic use
  • Thrombopoietin / therapeutic use

Substances

  • hetrombopag
  • Pyrazolones
  • Hydrazones
  • Thrombopoietin
  • Iron Chelating Agents