[低氧诱导因子脯氨酰羟化酶抑制剂治疗低风险骨髓增生异常综合征患者贫血的疗效和安全性分析]。

Q3 Medicine
Y Lyu, Z H Lin, L Yang, H Liu
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引用次数: 0

摘要

骨髓增生异常综合征是一组异质性的骨髓肿瘤性疾病,起源于造血干细胞,表现为病理性骨髓造血,极易转化为急性髓系白血病。对于低风险患者,治疗目标是改善造血功能和生活质量。罗沙司他是世界上首个口服小分子缺氧诱导因子脯氨酰羟化酶抑制剂,与传统的促红细胞生成素不同,它能通过多种机制纠正贫血。本研究通过回顾性分析低危骨髓增生异常综合征患者贫血、铁代谢、血脂和炎症指标的变化,评估其疗效和安全性,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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Efficacy and safety analysis of hypoxia-inducible factor prolyl hydroxylase inhibitors for anemia in low-risk myelodysplastic syndromes patients].

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.

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CiteScore
0.80
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