Gruszka Alicja M, Valli Debora, Alcalay Myriam
Department of Experimental Oncology, Istituto Europeo di Oncologia, Via Adamello 16, 20139 Milano, Italy.
Department of Oncology & Hemato-Oncology, University of Milan, Via Festa del Perdono 7, 20122 Milano, Italy.
Int J Hematol Oncol. 2017 Jun;6(2):43-53. doi: 10.2217/ijh-2017-0002. Epub 2017 Nov 17.
Although the treatment modalities for acute myeloid leukemia (AML) have not changed much over the past 40 years, distinct progress has been made in deciphering the basic biology underlying the pathogenesis of this group of hematological disorders. Studies show that AML development is a multicause, multistep and multipathway process. Accordingly, AMLs constitute a heterogeneous group of diseases. The thorough understanding of the molecular basis of AML is paving the way for better therapeutic approaches. Multiple novel drugs are being introduced and new, more efficient and less toxic formulations of conventional therapeutics are becoming available. Here, we review the recent advances in the comprehension of the molecular processes that lead to the onset of AML and its translation into clinical practice.
尽管在过去40年里,急性髓系白血病(AML)的治疗方式变化不大,但在解读这类血液系统疾病发病机制的基础生物学方面已取得显著进展。研究表明,AML的发展是一个多原因、多步骤和多途径的过程。因此,AML构成了一组异质性疾病。对AML分子基础的深入理解为更好的治疗方法铺平了道路。多种新型药物正在推出,传统疗法也有了更新、更高效且毒性更小的制剂。在此,我们综述了在理解导致AML发病的分子过程及其转化为临床实践方面的最新进展。