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骨髓增生异常综合征的新型药物

New agents in myelodysplastic syndromes.

作者信息

Jabbour Elias J, Giles Francis J

机构信息

Department of Leukemia, MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77063, USA.

出版信息

Curr Hematol Rep. 2005 May;4(3):191-9.

Abstract

Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal hematopoietic disorders characterized by ineffective hematopoiesis resulting in peripheral cytopenia and by increased progression to acute myeloid leukemia (AML). Therapeutic interventions for MDS other than allogeneic stem cell transplantation have been palliative. Novel and targeted therapeutic agents such as the inhibition of farnesyl transferases and receptor tyrosine kinases, more potent thalidomide analogs, arsenic trioxide, immunomodulating agents, hypomethylating agents, and histone deacetylase inhibitors have shown encouraging results and may offer durable benefit to patients with MDS. Further development of rational therapies and improvements in the outcome of patients with MDS are likely to emerge from an increased understanding of the pathophysiology of these diseases.

摘要

骨髓增生异常综合征(MDS)是一组异质性的克隆性造血疾病,其特征为造血无效导致外周血细胞减少,以及进展为急性髓系白血病(AML)的风险增加。除异基因干细胞移植外,MDS的治疗干预一直是姑息性的。新型靶向治疗药物,如法尼基转移酶抑制剂和受体酪氨酸激酶抑制剂、更强效的沙利度胺类似物、三氧化二砷、免疫调节剂、低甲基化剂和组蛋白去乙酰化酶抑制剂,已显示出令人鼓舞的结果,可能为MDS患者带来持久益处。随着对这些疾病病理生理学认识的增加,合理治疗的进一步发展以及MDS患者治疗结果的改善有望出现。

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