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铁螯合疗法在骨髓增生异常综合征中的血液学改善:临床数据、潜在机制和悬而未决的问题。

Hematologic improvement with iron chelation therapy in myelodysplastic syndromes: Clinical data, potential mechanisms, and outstanding questions.

机构信息

Hematology, St. Paul's Hospital and the University of British Columbia, Vancouver, BC, Canada.

Dept. of Hematology, Oncology and Clinical Immunology, Heinrich Heine University, Düsseldorf, Germany.

出版信息

Crit Rev Oncol Hematol. 2019 Sep;141:54-72. doi: 10.1016/j.critrevonc.2019.06.002. Epub 2019 Jun 10.

Abstract

Myelodysplastic syndromes (MDS) are clonal hematopoietic stem cell disorders characterized by cytopenias and progression to acute myeloid leukemia (AML). Although several treatments for MDS are available, the mainstay of therapy for most patients remains supportive care. This includes red blood cell (RBC) transfusion to correct anemia, which leads to iron overload. RBC transfusion dependence and iron overload portend inferior overall survival. Some studies indicate that iron chelation therapy (ICT) may have beneficial effects on clinical endpoints in MDS; however, these data are from non-randomized trials and the validity of the results is vigorously debated. A consistent observation in clinical studies of ICT in MDS has been hematologic improvement (HI) in some patients, including a reduction in RBC transfusion requirements and even transfusion independence. Here, we review data on HI with ICT in lower risk MDS, preclinical data examining mechanisms by which HI may occur, and identify areas for future investigation.

摘要

骨髓增生异常综合征(MDS)是一种克隆性造血干细胞疾病,其特征为血细胞减少和进展为急性髓系白血病(AML)。尽管有几种 MDS 治疗方法,但大多数患者的主要治疗方法仍然是支持性护理。这包括输血以纠正贫血,这会导致铁过载。RBC 输血依赖和铁过载预示着整体生存预后不良。一些研究表明,铁螯合疗法(ICT)可能对 MDS 的临床终点有有益的影响;然而,这些数据来自非随机试验,结果的有效性存在激烈争议。在 MDS 的 ICT 临床研究中,一个一致的观察结果是一些患者的血液学改善(HI),包括减少 RBC 输血需求甚至输血独立性。在这里,我们回顾了低危 MDS 中 ICT 的 HI 数据、检查 HI 可能发生的机制的临床前数据,并确定了未来研究的领域。

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