Nuhoğlu Kantarcı Eda, Eşkazan Ahmet Emre
Division of Hematology, Department of Internal Medicine, Cerrahpaşa Faculty of Medicine, Istanbul University-Cerrahpaşa, Istanbul, Turkey.
Division of Hematology, Department of Internal Medicine, Cerrahpaşa Faculty of Medicine, Istanbul University-Cerrahpaşa, Istanbul, Turkey.
Leuk Res. 2022 Mar;114:106808. doi: 10.1016/j.leukres.2022.106808. Epub 2022 Feb 9.
Acute myeloid leukemia (AML) is defined as a highly progressive heterogeneous hematologic malignancy characterized by loss of differentiation with uncontrolled proliferation of progenitor cells. 5-year overall survival rates are as low as 5-10% in adults above 60 years. Until recently, available treatment options for AML had remained mainly unchanged. Along with the development and usage of new generation drugs, novel therapeutic options in various settings began to alter the prognosis of the disease. FMS-like tyrosine kinase 3 (FLT3), a receptor largely expressed in myeloid progenitors, is thought to have a major role in the differentiation and maturation of hematopoietic precursors. Thus, aiming the inhibition of this pathway is gaining profound importance day by day. This review mainly focuses on the FLT3 inhibitor gilteritinib and its utilization in patients with AML. Current data from the most recent trials concerning gilteritinib and new advances are also discussed here.
急性髓系白血病(AML)被定义为一种高度进展性的异质性血液系统恶性肿瘤,其特征是祖细胞分化丧失且增殖不受控制。60岁以上成年人的5年总生存率低至5%-10%。直到最近,AML的可用治疗方案基本保持不变。随着新一代药物的开发和使用,各种情况下的新型治疗选择开始改变该疾病的预后。FMS样酪氨酸激酶3(FLT3)是一种在髓系祖细胞中大量表达的受体,被认为在造血前体细胞的分化和成熟中起主要作用。因此,针对该通路的抑制作用日益重要。本综述主要关注FLT3抑制剂吉列替尼及其在AML患者中的应用。本文还讨论了有关吉列替尼的最新试验的当前数据和新进展。