Roman Diaz Jaime L, Vazquez Martinez Mariola, Khimani Farhad
Moffitt Cancer Center, Bone Marrow Transplant and Cellular Immunotherapy, Tampa, FL 33612, USA.
Cancers (Basel). 2024 Feb 5;16(3):677. doi: 10.3390/cancers16030677.
Fifty years have passed since the development of the first chemotherapy regimen for treating acute myelogenous leukemia (AML), with the approval in 1973 of the cytarabine daunorubicin (7+3) regimen. Until recently, patients diagnosed with AML had very limited treatment options and depended primarily on chemotherapy in combinations, doses, or schedules of the same drugs. Patients with advanced age, comorbidities, or relapsed or refractory disease were left with no effective options for treatment. New advances in the understanding of the biology and the molecular and genetic changes associated with leukemogenesis, as well as recent advances in drug development, have resulted in the introduction over the last few years of novel therapeutic agents and approaches to the treatment of AML as well as a new classification of the disease. In this article, we will discuss the new classification of AML; the mechanisms, actions, and indications of the new targeted therapies; the chemotherapy combinations; and the potential role of cellular therapies as new treatment options for this terrible disease.
自1973年阿糖胞苷柔红霉素(7+3)方案获批,成为首个用于治疗急性髓系白血病(AML)的化疗方案以来,已经过去了50年。直到最近,被诊断为AML的患者治疗选择非常有限,主要依赖于相同药物的联合使用、剂量或给药方案进行化疗。老年患者、合并症患者或复发或难治性疾病患者没有有效的治疗选择。对白血病发生相关生物学以及分子和基因变化的新认识,以及药物开发的最新进展,导致在过去几年中引入了新型治疗药物和治疗AML的方法,以及该疾病的新分类。在本文中,我们将讨论AML的新分类;新靶向治疗的机制、作用和适应症;化疗联合方案;以及细胞治疗作为这种可怕疾病新治疗选择的潜在作用。