Service d'Hématologie Clinique, Hospital Avicenne, Assistance Publique-Hôpitaux de Paris (AP-HP), Université Paris XIII, Bobigny, France.
J Clin Oncol. 2010 Feb 1;28(4):562-9. doi: 10.1200/JCO.2009.23.8329. Epub 2009 Dec 21.
In a phase III randomized trial, azacitidine significantly prolonged overall survival (OS) compared with conventional care regimens (CCRs) in patients with intermediate-2- and high-risk myelodysplastic syndromes. Approximately one third of these patients were classified as having acute myeloid leukemia (AML) under current WHO criteria. This analysis compared the effects of azacitidine versus CCR on OS in this subgroup.
Patients were randomly assigned to receive subcutaneous azacitidine 75 mg/m(2)/d or CCR (best supportive care [BSC] only, low-dose cytarabine (LDAC), or intensive chemotherapy [IC]).
Of the 113 elderly patients (median age, 70 years) randomly assigned to receive azacitidine (n = 55) or CCR (n = 58; 47% BSC, 34% LDAC, 19% IC), 86% were considered unfit for IC. At a median follow-up of 20.1 months, median OS for azacitidine-treated patients was 24.5 months compared with 16.0 months for CCR-treated patients (hazard ratio = 0.47; 95% CI, 0.28 to 0.79; P = .005), and 2-year OS rates were 50% and 16%, respectively (P = .001). Two-year OS rates were higher with azacitidine versus CCR in patients considered unfit for IC (P = .0003). Azacitidine was associated with fewer total days in hospital (P < .0001) than CCR.
In older adult patients with low marrow blast count (20% to 30%) WHO-defined AML, azacitidine significantly prolongs OS and significantly improves several patient morbidity measures compared with CCR.
在一项 III 期随机试验中,与常规治疗方案(CCR)相比,阿扎胞苷显著延长了中危-2 级和高危骨髓增生异常综合征患者的总生存期(OS)。根据目前的世界卫生组织(WHO)标准,这些患者中有大约三分之一被归类为急性髓系白血病(AML)。本分析比较了阿扎胞苷与 CCR 对该亚组患者 OS 的影响。
患者被随机分配接受皮下阿扎胞苷 75mg/m2/d 或 CCR(仅最佳支持治疗[BSC]、低剂量阿糖胞苷[LDAC]或强化化疗[IC])。
在 113 名被随机分配接受阿扎胞苷(n=55)或 CCR(n=58;47%BSC、34%LDAC、19%IC)的老年患者(中位年龄 70 岁)中,86%的患者被认为不适合接受 IC。在中位随访 20.1 个月时,阿扎胞苷治疗患者的中位 OS 为 24.5 个月,而 CCR 治疗患者的中位 OS 为 16.0 个月(风险比=0.47;95%CI,0.28 至 0.79;P=0.005),2 年 OS 率分别为 50%和 16%(P=0.001)。在不适合接受 IC 的患者中,与 CCR 相比,阿扎胞苷治疗的患者 2 年 OS 率更高(P=0.0003)。与 CCR 相比,阿扎胞苷导致的总住院天数更少(P<0.0001)。
在骨髓原始细胞计数(20%至 30%)较低的老年 AML 患者中,与 CCR 相比,阿扎胞苷显著延长了 OS,并且显著改善了多项患者生存质量指标。