[低危骨髓增生异常综合征患者预后因素的研究进展--综述】。]

Q4 Medicine
Jiang-Nan Liu, Bao-An Chen, Jian Cheng
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引用次数: 0

摘要

骨髓增生异常综合征(MDS)是一组起源于造血干细胞的异质性克隆性疾病,以血细胞减少和极易转化为急性髓性白血病(AML)为特征。MDS 患者的预期存活时间差异很大,因此准确的预后评估尤为重要。目前,通常根据临床预后评分系统将 MDS 患者分为高危组(HR-MDS)和低危组(LR-MDS),但这些评分系统存在一定的局限性。LR-MDS患者占MDS患者的2/3,其疾病进展风险较低,预后较好,治疗主要依靠促红细胞生成药物、免疫抑制剂和成分输血。然而,仍有部分 LR-MDS 患者预后较差,现有的预后评分系统无法准确评估其预后。本综述简要总结了现有评估标准之外可能影响MDS患者预后的潜在因素,旨在为LR-MDS患者的预后评估和治疗提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Research Progress on Prognostic Factors in Patients with Lower-Risk Myelodysplastic Syndrome--Review].

Myelodysplastic syndrome (MDS) is a group of heterogeneous clonal disorders originating from hematopoietic stem cells, characterized by hemocytopenia and a high risk of transformation to acute myeloid leukemia (AML). The expected survival time of MDS patients varies widely, and accurate prognostic assessment is particularly important. Currently, patients with MDS are usually classified into a higher-risk group (HR-MDS) and a lower-risk group (LR-MDS) based on clinical prognostic scoring systems, but these scoring systems have certain limitations. Patients with LR-MDS account for 2/3 of MDS patients, with a lower risk of disease progression and a better prognosis, and their treatment mainly relies on erythropoiesis-stimulating agents, immunosuppressants and component transfusion. However, some LR-MDS patients still have poor prognosis, and the existing prognostic scoring systems cannot accurately evaluate their prognosis. In this review, the potential factors that may influence the prognosis of MDS patients beyond the existing assessment criteria were briefly summarized, with the aim of providing reference for the prognosis evaluation and treatment of LR-MDS patients.

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来源期刊
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
7331
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