去铁斯若
医学
再生障碍性贫血
内科学
析因分析
胃肠病学
耐火材料(行星科学)
螯合疗法
铁蛋白
贫血
血小板生成素
地中海贫血
造血
骨髓
生物
天体生物学
物理
干细胞
遗传学
作者
Wenrui Yang,Xin Zhao,Guangsheng He,Hong Chang,Bing Han,Sujun Gao,Shunqing Wang,Tong Chen,Fei Li,Yi Wang,Xiaoyan Ge,Rong Fu,Zheng Ge,Yingmei Li,Hong Liu,Xinjian Liu,Miao Miao,Liansheng Zhang,Fengkui Zhang
标识
DOI:10.1007/s00277-022-04968-8
摘要
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.
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