Department of Hematology/Oncology, University of California, Los Angeles, Box 957059, Suite 2333 PVUB, Los Angeles, CA 90095, USA.
Curr Hematol Malig Rep. 2009 Jan;4(1):10-6. doi: 10.1007/s11899-009-0002-9.
Myelodysplastic syndromes (MDS) are a diverse group of disorders characterized by disorderly and ineffective hematopoiesis. Patients suffer morbidity from associated cytopenias that result in an increased risk of infection, transfusion-dependent anemia, and bleeding. Despite the variable risk of transformation to acute leukemia, the majority of deaths are due to bone marrow failure. No truly effective treatment exists for MDS, and therapy usually focuses on reducing or preventing complications of the disease. Identification of potential cellular and molecular targets, such as epigenetic modification, has led to novel therapeutic approaches in recent years. An increasing number of diagnostic markers, prognostic parameters, and therapeutic strategies are available and becoming widely accepted.
骨髓增生异常综合征(MDS)是一组以造血功能紊乱和无效为特征的异质性疾病。患者因相关细胞减少而出现发病率增加,导致感染、输血依赖性贫血和出血的风险增加。尽管向急性白血病转化的风险不同,但大多数死亡是由于骨髓衰竭。MDS 没有真正有效的治疗方法,治疗通常侧重于减少或预防疾病的并发症。近年来,对表观遗传修饰等潜在细胞和分子靶点的鉴定,导致了新的治疗方法。越来越多的诊断标志物、预后参数和治疗策略正在被广泛接受。