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低危骨髓增生异常综合征中的阿扎胞苷。

Azacitidine in lower-risk myelodysplastic syndromes.

机构信息

UF Ematologia, Azienda Ospedaliero-Universitaria (AOU) Careggi, Università degli Studi di Firenze, Florence, Italy.

出版信息

Leuk Res. 2009 Dec;33 Suppl 2:S22-6. doi: 10.1016/S0145-2126(09)70230-9.

Abstract

Azacitidine is the first agent to significantly prolong overall survival (OS) compared with conventional care regimens in patients with higher-risk myelodysplastic syndromes (MDS). Here, we review currently available data on azacitidine treatment in lower-risk MDS. In a phase III study, a subset of patients with lower-risk MDS treated with azacitidine achieved an overall response rate (ORR) of 60% and a longer median OS compared with supportive care (44 vs 27 months). In a phase II study investigating various azacitidine dose schedules, the hematological improvement rate was approximately 50% in lower-risk patients; most patients who achieved transfusion independence were also lower-risk. A further retrospective study reported an ORR of 52% in MDS lower-risk patients who received > or = 4 cycles of therapy. Preliminary data for azacitidine combination therapy with erythropoietin, granulocyte colony-stimulating factor, and valproic acid are intriguing but should be treated with caution. These results suggest the feasibility and effectiveness of azacitidine in the treatment of patients with lower-risk MDS.

摘要

阿扎胞苷是首个与高危骨髓增生异常综合征(MDS)患者的常规治疗方案相比,显著延长总生存期(OS)的药物。在此,我们回顾了阿扎胞苷治疗低危 MDS 的现有数据。在一项 III 期研究中,接受阿扎胞苷治疗的低危 MDS 患者亚组总缓解率(ORR)为 60%,中位 OS 长于支持治疗(44 个月 vs 27 个月)。在一项研究各种阿扎胞苷剂量方案的 II 期研究中,低危患者的血液学改善率约为 50%;大多数实现输血独立性的患者也是低危。进一步的回顾性研究报告称,接受 > 4 个周期治疗的 MDS 低危患者的 ORR 为 52%。阿扎胞苷联合促红细胞生成素、粒细胞集落刺激因子和丙戊酸钠治疗的初步数据很有趣,但应谨慎对待。这些结果表明阿扎胞苷治疗低危 MDS 患者是可行和有效的。

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