骨髓纤维化
骨髓增生异常综合症
贫血
医学
无效红细胞生成
再生障碍性贫血
内科学
免疫学
红细胞生成
骨髓
作者
Pierre Fenaux,Jean‐Jacques Kiladjian,Uwe Platzbecker
出处
期刊:Blood
[American Society of Hematology]
日期:2019-01-03
卷期号:133 (8): 790-794
被引量:89
标识
DOI:10.1182/blood-2018-11-876888
摘要
Abstract Anemia of lower-risk myelodysplastic syndromes (MDSs) and primary myelofibrosis (PMF) generally becomes resistant to available treatments, leading to red blood cell (RBC) transfusions, iron overload, shortened survival, and poor quality of life. The transforming growth factor-β superfamily, including activins and growth differentiation factors (GDFs), is aberrantly expressed in lower-risk MDSs and PMF. Luspatercept (and sotatercept), ligand traps that particularly inhibit GDF11, lead to RBC transfusion independence in 10% to 50% of lower-risk MDSs resistant to available treatments, and have started to be used in PMF.
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