Cogle Christopher R, Scott Bart L, Boyd Thomas, Garcia-Manero Guillermo
Division of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida, USA
Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Oncologist. 2015 Dec;20(12):1404-12. doi: 10.1634/theoncologist.2015-0165. Epub 2015 Oct 13.
The myelodysplastic syndromes (MDS) comprise a heterogeneous group of clonal myeloid malignancies characterized by multilineage cytopenias, recurrent cytogenetic abnormalities, and risk of progression to acute myeloid leukemia (AML). AML, which can occur de novo as well as secondary to MDS, is characterized by malignant clones of myeloid lineage in the bone marrow and peripheral blood, with dissemination into tissues. The cytidine nucleoside analog and epigenetic modifier azacitidine is approved in the U.S. for the treatment of all French-American-British subtypes of MDS and in many countries for the treatment of AML with 20%-30% blasts and multilineage dysplasia according to the World Health Organization classification. Benefits of azacitidine treatment of patients with AML with >30% blasts have also been shown in a recent phase III trial. Oral administration of azacitidine may enhance patient convenience, eliminate injection-site reactions, allow for alternative dosing and scheduling, and enable long-term treatment. Phase I studies with oral azacitidine (CC-486) have shown biological activity, clinical responses, and tolerability in patients with MDS and AML. Extended dosing schedules of oral azacitidine (for 14 or 21 days of 28-day cycles) are currently under investigation as frontline therapy in patients with lower risk MDS, as maintenance therapy for patients with AML not eligible for stem cell transplant, and as maintenance therapy for patients with MDS or AML following stem cell transplant. This review presents clinical data supporting the use of injectable azacitidine in MDS and AML and examines the rationale for and results of the clinical development of oral azacitidine.
骨髓增生异常综合征(MDS)是一组异质性的克隆性髓系恶性肿瘤,其特征为多系血细胞减少、反复出现的细胞遗传学异常以及进展为急性髓系白血病(AML)的风险。AML可原发发生,也可继发于MDS,其特征为骨髓和外周血中髓系谱系的恶性克隆,并可扩散至组织。胞苷核苷类似物及表观遗传修饰剂阿扎胞苷在美国被批准用于治疗所有法国-美国-英国亚型的MDS,在许多国家被批准用于治疗根据世界卫生组织分类有20%-30%原始细胞和多系发育异常的AML。最近一项III期试验也显示了阿扎胞苷治疗原始细胞>30%的AML患者的益处。口服阿扎胞苷可能会提高患者的便利性,消除注射部位反应,允许采用替代给药方式和给药方案,并能进行长期治疗。口服阿扎胞苷(CC-486)的I期研究已显示出对MDS和AML患者具有生物学活性、临床反应和耐受性。目前正在研究口服阿扎胞苷的延长给药方案(28天周期中的14天或21天),作为低危MDS患者的一线治疗、不符合干细胞移植条件的AML患者的维持治疗以及干细胞移植后MDS或AML患者的维持治疗。本综述展示了支持在MDS和AML中使用注射用阿扎胞苷的临床数据,并探讨了口服阿扎胞苷临床开发的基本原理和结果。