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骨髓增生异常综合征的最新进展

Recent advances in myelodysplastic syndromes.

作者信息

Shadduck Richard K, Latsko Joan M, Rossetti James M, Haq Bushra, Abdulhaq Haifaa

机构信息

Western Pennsylvania Cancer Institute, Western Pennsylvania Hospital, Pittsburgh, PA 15224, USA.

出版信息

Exp Hematol. 2007 Apr;35(4 Suppl 1):137-43. doi: 10.1016/j.exphem.2007.01.022.

Abstract

Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal bone marrow disorders characterized by both bone marrow failure and a propensity for development of acute myeloid leukemia. The incidence of these conditions has risen sharply over the past several years, making them the most common malignant bone marrow disorders. While the majority of patients are diagnosed with low-grade disease, approximately two-thirds will succumb to complications of peripheral blood cytopenias or progression to acute leukemia. In recent years, there has been striking progress in our understanding of the pathogenesis of these disorders. For example, the recognition of the roles of angiogenesis and cytokine abnormalities in the development of these diseases led to clinical trials with agents such as thalidomide, which yielded encouraging erythroid responses. Subsequent work with the thalidomide derivative lenalidomide resulted in marked erythroid and cytogenetic responses in individuals with the 5q- abnormality. Additionally, the identification of hypermethylation as an important aspect in the pathogenesis of these and other hematological diseases led to clinical trials utilizing the demethylating agents azacitidine and decitibine. These agents are now known to result in trilineage responses in 30% to 50% of patients with MDS with as many as 20% achieving partial or complete remissions. These results have altered the natural history of these diseases in a significant number of patients. Investigators anticipate that further studies with tyrosine kinase, histone deacetylase, and farnesyl transferase inhibitors will contribute to already promising attempts to reverse or block the pathogenesis of these diseases. Other novel agents are being evaluated as investigators continue to make progress for patients affected by these disorders.

摘要

骨髓增生异常综合征(MDS)是一组异质性的克隆性骨髓疾病,其特征为骨髓衰竭以及有发展为急性髓系白血病的倾向。在过去几年中,这些病症的发病率急剧上升,使其成为最常见的恶性骨髓疾病。虽然大多数患者被诊断为低级别疾病,但约三分之二的患者会死于外周血细胞减少症的并发症或进展为急性白血病。近年来,我们对这些疾病发病机制的理解取得了显著进展。例如,认识到血管生成和细胞因子异常在这些疾病发展中的作用,引发了使用沙利度胺等药物的临床试验,该试验产生了令人鼓舞的红系反应。随后对沙利度胺衍生物来那度胺的研究,使具有5q-异常的个体出现了显著的红系和细胞遗传学反应。此外,发现高甲基化是这些及其他血液系统疾病发病机制中的一个重要方面,从而引发了使用去甲基化药物阿扎胞苷和地西他滨的临床试验。现在已知这些药物可使30%至50%的MDS患者出现三系反应,多达2 = 0%的患者实现部分或完全缓解。这些结果在相当数量的患者中改变了这些疾病的自然病程。研究人员预计,对酪氨酸激酶、组蛋白脱乙酰酶和法尼基转移酶抑制剂的进一步研究,将有助于在逆转或阻断这些疾病发病机制的已有前景的尝试中发挥作用。随着研究人员继续在受这些疾病影响的患者身上取得进展,其他新型药物也在接受评估。

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