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Sequential Treatment with Cytarabine and Decitabine Has an Increased Anti-Leukemia Effect Compared to Cytarabine Alone in Xenograft Models of Childhood Acute Myeloid Leukemia

机译:与单独使用阿糖胞苷相比在儿童急性髓样白血病的异种移植模型中阿糖胞苷和地西他滨序贯治疗的抗白血病作用增强

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摘要

The current interest in epigenetic priming is underpinned by the belief that remodelling of the epigenetic landscape will sensitise tumours to subsequent therapy. In this pre-clinical study, paediatric AML cells expanded in culture and primary AML xenografts were treated with decitabine, a DNA demethylating agent, and cytarabine, a frontline cytotoxic agent used in the treatment of AML, either alone or in combination. Sequential treatment with decitabine and cytarabine was found to be more effective in reducing tumour burden than treatment with cytarabine alone suggesting that the sequential delivery of these agents may a have real clinical advantage in the treatment of paediatric AML. However we found no evidence to suggest that this outcome was dependent on priming with a hypomethylating agent, as the benefits observed were independent of the order in which these drugs were administered.
机译:当前对表观遗传启动的兴趣是基于这样的信念,即表观遗传格局的重塑将使肿瘤对后续治疗敏感。在这项临床前研究中,小儿AML细胞在培养物中扩增,并且原发性AML异种移植物分别用DNA脱甲基化剂地西他滨和用于治疗AML的一线细胞毒性剂阿糖胞苷单独或联合治疗。发现用地西他滨和阿糖胞苷相继治疗比单独用阿糖胞苷治疗更有效的减轻肿瘤负担,这表明这些药物的顺序递送在治疗小儿AML中可能具有真正的临床优势。但是,我们发现没有证据表明该结果取决于使用次甲基化剂进行灌注,因为观察到的益处与这些药物的给药顺序无关。

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