Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, Georgia.
Division of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Cancer. 2020 Nov 1;126(21):4668-4677. doi: 10.1002/cncr.32904. Epub 2020 Aug 7.
Recent years have seen tremendous advances in treating acute myeloid leukemia (AML), largely because of progress in understanding the genetic basis of the disease. The US Food and Drug Administration approved 7 agents for AML in the last 2 years: the first new drugs in decades. In this review, the authors discuss these new approvals in the backdrop of an overall strategy for treating AML today. Treating AML in the modern era requires: 1) access to and use of upfront genetic and cytogenetic testing, not only to describe prognosis but also to help identify the best available therapy; 2) effectively working new therapies into a conventional backbone of treatment, including transplantation; and 3) continued commitment to clinical trials designed to capitalize on advances in genetics and immunology to foster the next wave of drug approvals.
近年来,急性髓系白血病(AML)的治疗取得了巨大进展,这在很大程度上要归功于人们对该疾病遗传基础的理解的进步。在过去的两年中,美国食品和药物管理局(FDA)批准了 7 种 AML 药物:这是几十年来的第一批新药。在这篇综述中,作者讨论了在当今治疗 AML 的整体策略背景下对这些新批准药物的看法。在现代时代治疗 AML 需要:1)能够并使用初始基因和细胞遗传学检测,不仅要描述预后,还要帮助确定最佳可用疗法;2)将新疗法有效地纳入常规治疗基础中,包括移植;3)继续致力于临床试验,旨在利用遗传学和免疫学的进步,为下一波药物批准创造条件。