Rowe Jacob M
Technion, Israel Instittue of Technology, 31096 Haifa, Israel; Rambam Health Care Campus, Department of Hematology, Haifa, Israel; Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Shaare Zedek Medical Center, Department of Hematology, Jerusalem 91031, Israel.
Best Pract Res Clin Haematol. 2015 Jun-Sep;28(2-3):69-72. doi: 10.1016/j.beha.2015.10.002. Epub 2015 Oct 22.
Distinct progress has been made in recent years in the therapy of acute leukemia. For acute myeloid leukemia (AML), this progress has been anchored in the increased understanding of genomic complexity. Multiple targets and the relationships among them pose new challenges along with new possibilities for the development of targeted therapies. A number of new drugs are in early clinical development for AML, one of which centers on the role of isocitrate dehydrogenase (IDH) in malignancy. Epigenetic modulation, intracellular pathways, and the microenvironment are all being explored for possible therapies to treat AML. Dramatic clinical progress has also been made in therapy of acute lymphoblastic leukemia (ALL) with the rapid approval of blinatumomab, a bispecific T-cell engager antibody. Yet caution must also be exercised-not every mutation is an epigenetic target and early publication of clinical data is often misleading. Until the survival outcome for adult patients with acute leukemia improves, further inquiry into the biology of the disease and progress in the development of new therapies are needed.
近年来,急性白血病的治疗取得了显著进展。对于急性髓系白血病(AML),这一进展源于对基因组复杂性的深入了解。多个靶点及其相互关系带来了新的挑战,同时也为靶向治疗的发展提供了新的可能性。一些新药正处于AML的早期临床开发阶段,其中一种以异柠檬酸脱氢酶(IDH)在恶性肿瘤中的作用为核心。表观遗传调控、细胞内信号通路和微环境都在被探索用于治疗AML的可能疗法。在急性淋巴细胞白血病(ALL)的治疗方面也取得了显著的临床进展,双特异性T细胞衔接抗体blinatumomab迅速获批。然而,也必须谨慎——并非每个突变都是表观遗传靶点,临床数据的早期公布往往具有误导性。在成年急性白血病患者的生存结果得到改善之前,需要进一步探究该疾病的生物学特性并推动新疗法的开发进展。