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中危-2 级和高危骨髓增生异常综合征中阿扎胞苷试验的综述。

Review of azacitidine trials in Intermediate-2-and High-risk myelodysplastic syndromes.

机构信息

Service d'Hématologie Clinique, Hôpital Avicenne, Assistance Publique-Hôpitaux de Paris, Université Paris XIII, Bobigny, France.

出版信息

Leuk Res. 2009 Dec;33 Suppl 2:S7-11. doi: 10.1016/S0145-2126(09)70227-9.

Abstract

The efficacy of azacitidine, a cytosine nucleoside analog, has been demonstrated in two large phase III trials in myelodysplastic syndromes (MDS) patients, primarily in higher-risk patients. In the Cancer and Leukemia Group B (CALGB) study (lower-and higher-risk MDS patients; n = 191) azacitidine significantly prolonged median time-to-progression to acute myeloid leukemia or death (21 vs 13 months for supportive care; p = 0.007). The AZA-001 trial (Intermediate-2-and High-risk MDS patients; n = 358) showed azacitidine significantly prolonged median overall survival compared with conventional care regimens (24.5 vs 15.0 months; p = 0.0001). These results establish azacitidine as a reference first-line treatment in patients with Intermediate-2-and High-risk MDS who are not immediate candidates for allogeneic stem cell transplantation.

摘要

阿扎胞苷是一种胞嘧啶核苷类似物,在两项大型 III 期临床试验中已证明其在骨髓增生异常综合征(MDS)患者中的疗效,主要是在高危患者中。在癌症和白血病组 B(CALGB)研究(低危和高危 MDS 患者;n = 191)中,阿扎胞苷显著延长了向急性髓系白血病或死亡进展的中位时间(支持性治疗为 21 个月 vs 13 个月;p = 0.007)。AZA-001 试验(中-2 危和高危 MDS 患者;n = 358)表明,与常规治疗方案相比,阿扎胞苷显著延长了中位总生存期(24.5 个月 vs 15.0 个月;p = 0.0001)。这些结果确立了阿扎胞苷作为中-2 危和高危 MDS 患者的一线治疗参考,这些患者不是异基因干细胞移植的直接候选者。

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