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低危骨髓增生异常综合征患者贫血应用缺氧诱导因子脯氨酰羟化酶抑制剂的疗效与安全性分析

[Efficacy and safety analysis of hypoxia-inducible factor prolyl hydroxylase inhibitors for anemia in low-risk myelodysplastic syndromes patients].

作者信息

Lyu Y, Lin Z H, Yang L, Liu H

机构信息

Department of Hematology, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong 226001, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2024 Mar 14;45(3):290-293. doi: 10.3760/cma.j.cn121090-20230825-00089.

DOI:10.3760/cma.j.cn121090-20230825-00089
PMID:38716602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11078660/
Abstract

Myelodysplastic syndromes is a heterogeneous group of myeloid neoplastic disorders originating from hematopoietic stem cells and manifesting as pathological bone marrow hematopoiesis and a high risk of transformation to acute myeloid leukemia. In low-risk patients, the therapeutic goal is to improve hematopoiesis and quality of life. Roxadustat is the world's first oral small-molecule hypoxia-inducible factor prolyl hydroxylase inhibitor, which, unlike conventional erythropoietin, corrects anemia through various mechanisms. In this study, we retrospectively analyzed the changes in anemia, iron metabolism, lipids and inflammatory indexes in patients with low-risk myelodysplastic syndromes to evaluate its therapeutic efficacy and safety, and to provide theoretical and practical data for the application of roxadustat in myelodysplastic syndromes.

摘要

骨髓增生异常综合征是一组异质性的髓系肿瘤性疾病,起源于造血干细胞,表现为病理性骨髓造血以及转化为急性髓系白血病的高风险。在低危患者中,治疗目标是改善造血功能和生活质量。罗沙司他是全球首个口服小分子低氧诱导因子脯氨酰羟化酶抑制剂,与传统促红细胞生成素不同,它通过多种机制纠正贫血。在本研究中,我们回顾性分析了低危骨髓增生异常综合征患者贫血、铁代谢、血脂及炎症指标的变化,以评估其治疗效果和安全性,并为罗沙司他在骨髓增生异常综合征中的应用提供理论和实践数据。

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[Efficacy and safety analysis of hypoxia-inducible factor prolyl hydroxylase inhibitors for anemia in low-risk myelodysplastic syndromes patients].低危骨髓增生异常综合征患者贫血应用缺氧诱导因子脯氨酰羟化酶抑制剂的疗效与安全性分析
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J Clin Pharmacol. 2020 Nov;60(11):1432-1440. doi: 10.1002/jcph.1648. Epub 2020 Jun 30.
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Roxadustat for Treating Anemia in Patients with CKD Not on Dialysis: Results from a Randomized Phase 3 Study.罗沙司他治疗未透析慢性肾脏病患者贫血的随机 3 期研究结果。
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引用本文的文献

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Hypoxia-inducible factor-prolyl hydroxylase inhibitors in treatment of anemia with chronic disease.缺氧诱导因子-脯氨酰羟化酶抑制剂治疗慢性病贫血
Chin Med J (Engl). 2025 Jun 20;138(12):1424-1432. doi: 10.1097/CM9.0000000000003470. Epub 2025 May 23.

本文引用的文献

1
New Approaches to Myelodysplastic Syndrome Treatment.骨髓增生异常综合征治疗的新方法。
Curr Treat Options Oncol. 2022 May;23(5):668-687. doi: 10.1007/s11864-022-00965-1. Epub 2022 Mar 23.
2
Roxadustat for the treatment of anemia in patients with lower-risk myelodysplastic syndrome: Open-label, dose-selection, lead-in stage of a phase 3 study.罗沙司他治疗低危骨髓增生异常综合征患者的贫血:一项 3 期研究的开放标签、剂量选择、导入阶段。
Am J Hematol. 2022 Feb 1;97(2):174-184. doi: 10.1002/ajh.26397. Epub 2021 Nov 9.
3
The Clinical Significance of Iron Overload and Iron Metabolism in Myelodysplastic Syndrome and Acute Myeloid Leukemia.骨髓增生异常综合征和急性髓系白血病中铁过载和铁代谢的临床意义。
Front Immunol. 2021 Feb 19;11:627662. doi: 10.3389/fimmu.2020.627662. eCollection 2020.
4
Luspatercept in Patients with Lower-Risk Myelodysplastic Syndromes.芦可替尼治疗低危骨髓增生异常综合征患者的疗效。
N Engl J Med. 2020 Jan 9;382(2):140-151. doi: 10.1056/NEJMoa1908892.
5
Setting Fire to ESA and EMA Resistance: New Targeted Treatment Options in Lower Risk Myelodysplastic Syndromes.点燃 ESA 和 EMA 抵抗:低危骨髓增生异常综合征的新靶向治疗选择。
Int J Mol Sci. 2019 Aug 7;20(16):3853. doi: 10.3390/ijms20163853.
6
Roxadustat for Anemia in Patients with Kidney Disease Not Receiving Dialysis.罗沙司他治疗未接受透析的肾病患者的贫血。
N Engl J Med. 2019 Sep 12;381(11):1001-1010. doi: 10.1056/NEJMoa1813599. Epub 2019 Jul 24.
7
[Chinese guidelines for diagnosis and treatment of myelodysplastic syndromes (2019)].《中国骨髓增生异常综合征诊断与治疗指南(2019年版)》
Zhonghua Xue Ye Xue Za Zhi. 2019 Feb 14;40(2):89-97. doi: 10.3760/cma.j.issn.0253-2727.2019.02.001.
8
Roxadustat: First Global Approval.罗沙司他:全球首次获批。
Drugs. 2019 Apr;79(5):563-572. doi: 10.1007/s40265-019-01077-1.
9
A phase 3 randomized, placebo-controlled study assessing the efficacy and safety of epoetin-α in anemic patients with low-risk MDS.一项评估低危 MDS 贫血患者使用促红细胞生成素-α的疗效和安全性的 3 期随机、安慰剂对照研究。
Leukemia. 2018 Dec;32(12):2648-2658. doi: 10.1038/s41375-018-0118-9. Epub 2018 Mar 30.
10
Hypoxia-inducible factor 1α activates insulin-induced gene 2 (Insig-2) transcription for degradation of 3-hydroxy-3-methylglutaryl (HMG)-CoA reductase in the liver.缺氧诱导因子1α激活胰岛素诱导基因2(Insig-2)的转录,以促进肝脏中3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶的降解。
J Biol Chem. 2017 Jun 2;292(22):9382-9393. doi: 10.1074/jbc.M117.788562. Epub 2017 Apr 17.