Department of Leukemia, University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 428, Houston, TX 77030, USA.
Best Pract Res Clin Haematol. 2013 Sep;26(3):253-9. doi: 10.1016/j.beha.2013.10.005. Epub 2013 Oct 16.
Relapse after achieving a prior response remains one of the most important obstacles to improving the outcome of patients with acute myeloid leukemia (AML). Although overall, the majority of patients with disease relapse do poorly, this is by no means uniform and a number of predictors of outcome have been identified. Previously, most trials of investigational agents in the setting of disease relapse in AML have accrued a wide range of patients with widely different patient and disease characteristics. With increased understanding of the biology of the neoplastic change in AML, and better identification of disease subsets based on their molecular characterization, target-specific novel agents are being developed that will hopefully lead to better strategies, not only for treating relapsed disease, but also for the initial induction treatment.
在实现先前缓解后复发仍然是改善急性髓细胞白血病 (AML) 患者预后的最重要障碍之一。尽管总体而言,大多数疾病复发的患者预后不佳,但这绝非一致,并且已经确定了一些预后预测因素。以前,在 AML 疾病复发的情况下,大多数关于研究药物的试验都招募了广泛不同的患者,这些患者具有广泛不同的患者和疾病特征。随着对 AML 中肿瘤变化生物学的深入了解,以及基于其分子特征更好地确定疾病亚组,正在开发针对特定靶点的新型药物,这有望为更好的策略提供希望,不仅用于治疗复发疾病,而且用于初始诱导治疗。