Koppel Ahrin, Schiller Gary
Department of Hematology/Oncology, University of California, Los Angeles, Box 957059, Suite 2333 PVUB, Los Angeles, CA 90095, USA.
Curr Oncol Rep. 2008 Sep;10(5):372-8. doi: 10.1007/s11912-008-0058-z.
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)是一组异质性疾病,其特征为造血紊乱且无效。患者因相关血细胞减少而发病,这会导致感染风险增加、依赖输血的贫血以及出血。尽管转化为急性白血病的风险各不相同,但大多数死亡是由于骨髓衰竭。目前尚无真正有效的MDS治疗方法,治疗通常侧重于减少或预防该疾病的并发症。近年来,对潜在细胞和分子靶点的识别,如表观遗传修饰,已带来了新的治疗方法。越来越多的诊断标志物、预后参数和治疗策略可供使用并被广泛接受。