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首页> 外文期刊>British Journal of Haematology >Utility of a clinical risk score to identify high-risk patients with de novo acute myeloid leukaemia in first remission after high-dose cytarabine (HiDAC) based induction chemotherapy
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Utility of a clinical risk score to identify high-risk patients with de novo acute myeloid leukaemia in first remission after high-dose cytarabine (HiDAC) based induction chemotherapy

机译:临床风险评分用于确定基于大剂量阿糖胞苷(HiDAC)的诱导化疗后首次缓解的初发急性髓性白血病的高危患者

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摘要

Induction chemotherapy combining anthracyclines and cytarabine has been the cornerstone of therapy for acute myeloid leukaemia (AML) for almost four decades. Several groups, including the Australasian Leukaemia and Lymphoma Group (ALLG), have incorporated high-dose cytarabine (HiDAC) into the initial induction regimen, resulting in very high rates (~80%) of first cycle complete remission (CR) and improved progression-free survival outcomes (Bishop et al, 1996; Bradstock et al, 2005; Braess et al, 2009; Ravandi et al, 2010).
机译:近二十年来,结合蒽环类药物和阿糖胞苷的诱导化疗一直是治疗急性髓性白血病(AML)的基石。包括澳大利亚白血病和淋巴瘤组(ALLG)在内的几组已将高剂量阿糖胞苷(HiDAC)纳入初始诱导方案,导致第一周期完全缓解(CR)的发生率非常高(〜80%),并改善了进展无生存期的结果(Bishop等,1996; Bradstock等,2005; Braess等,2009; Ravandi等,2010)。

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