Ishii Hiroto, Yano Shingo
Division of Clinical Oncology & Hematology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo 1058461, Japan.
Cancers (Basel). 2022 Jun 5;14(11):2806. doi: 10.3390/cancers14112806.
Acute myeloid leukemia (AML) is a genetically heterogeneous hematological malignancy. Chromosomal and genetic analyses are important for the diagnosis and prognosis of AML. Some patients experience relapse or have refractory disease, despite conventional cytotoxic chemotherapies and allogeneic transplantation, and a variety of new agents and treatment strategies have emerged. After over 20 years during which no new drugs became available for the treatment of AML, the CD33-targeting antibody-drug conjugate gemtuzumab ozogamicin was developed. This is currently used in combination with standard chemotherapy or as a single agent. CPX-351, a liposomal formulation containing daunorubicin and cytarabine, has become one of the standard treatments for secondary AML in the elderly. FMS-like tyrosine kinase 3 () inhibitors and isocitrate dehydrogenase 1/2 ( 1/2) inhibitors are mainly used for AML patients with actionable mutations. In addition to hypomethylating agents and venetoclax, a B-cell lymphoma-2 inhibitor is used in frail patients with newly diagnosed AML. Recently, tumor protein p53 inhibitors, cyclin-dependent kinase inhibitors, and NEDD8 E1-activating enzyme inhibitors have been gaining attention, and a suitable strategy for the use of these drugs is required. Antibody drugs targeting cell-surface markers and immunotherapies, such as antibody-drug conjugates and chimeric antigen receptor T-cell therapy, have also been developed for AML.
急性髓系白血病(AML)是一种具有基因异质性的血液系统恶性肿瘤。染色体和基因分析对于AML的诊断和预后至关重要。尽管采用了传统的细胞毒性化疗和异基因移植,但仍有一些患者会复发或患有难治性疾病,因此出现了多种新的药物和治疗策略。在超过20年没有新药可用于治疗AML之后,开发了靶向CD33的抗体药物偶联物吉妥珠单抗奥唑米星。目前它与标准化疗联合使用或作为单一药物使用。CPX-351是一种含有柔红霉素和阿糖胞苷的脂质体制剂,已成为老年继发性AML的标准治疗方法之一。FMS样酪氨酸激酶3(FLT3)抑制剂和异柠檬酸脱氢酶1/2(IDH1/2)抑制剂主要用于具有可操作突变的AML患者。除了去甲基化药物和维奈克拉外,B细胞淋巴瘤-2抑制剂用于新诊断的体弱AML患者。最近,肿瘤蛋白p53抑制剂、细胞周期蛋白依赖性激酶抑制剂和NEDD8 E1激活酶抑制剂受到关注,需要一种合适的这些药物使用策略。针对细胞表面标志物的抗体药物以及免疫疗法,如抗体药物偶联物和嵌合抗原受体T细胞疗法,也已被开发用于AML。