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Azacitidine: in myelodysplastic syndromes.

机译:阿扎胞苷:在骨髓增生异常综合症中。

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摘要

Azacitidine, a pyrimidine analogue, is an antineoplastic agent that acts mainly by causing hypomethylation of cytosine residues in newly replicated DNA and has shown efficacy in the treatment of myelodysplatic syndromes (MDS). In a randomised controlled trial in patients with MDS (n=191), subcutaneous azacitidine 75-100 mg/m2/day in 7-day cycles every 28 days with continuing supportive care produced a significantly higher response rate (including reductions in rate of transformation to acute myeloid leukaemia and transfusion requirements) than that seen with supportive care alone (60% vs 5%; p<0.001). Patients (n=49) who were switched from supportive care to azacitidine after 4 months also showed a 47% response rate. The clinical response in patients receiving azacitidine was associated with significant (p
机译:阿扎胞苷(一种嘧啶类似物)是一种抗肿瘤药,主要通过引起新复制的DNA中胞嘧啶残基的低甲基化而发挥作用,并已显示出治疗骨髓增生异常综合征(MDS)的功效。在MDS患者(n = 191)的一项随机对照试验中,在持续支持治疗的情况下,每28天皮下注射阿扎胞苷75-100 mg / m2 /天,每7天一次,可产生更高的缓解率(包括降低转化率),每28天一次急性髓细胞性白血病和输血需求)(单独支持治疗时的发生率)(60%比5%; p <0.001)。 4个月后从支持治疗转为阿扎胞苷的患者(n = 49)也显示出47%的缓解率。与支持治疗接受者相比,接受阿扎胞苷治疗的患者的临床反应与多种健康相关生活质量指标(包括评估疲劳和身体机能的指标)显着改善(p <或= 0.015)有关。鉴于MDS患者的预后严峻,通常对阿扎胞苷的耐受性良好,具有常见但短暂的骨髓毒性。在治疗过程中,不良事件的严重程度或发生频率并未增加。

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