| Literature DB >> 36220881 |
Wenrui Yang1, Xin Zhao1, Guangsheng He2, Hong Chang3, Bing Han4, Sujun Gao5, Shunqing Wang6, Tong Chen7, Fei Li8, Yi Wang9, Xiaoyan Ge10, Rong Fu11, Zheng Ge12, Yingmei Li13, Hong Liu14, Xinjian Liu15, Miao Miao16, Liansheng Zhang17, Fengkui Zhang18.
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.Entities:
Keywords: Aplastic anemia; Hetrombopag; Iron chelation
Year: 2022 PMID: 36220881 DOI: 10.1007/s00277-022-04968-8
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 4.030