Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Rabin Medical Center and Faculty of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.
Am J Hematol. 2023 Mar;98(3):502-526. doi: 10.1002/ajh.26822. Epub 2023 Jan 13.
Acute myeloid leukemia (AML) is a frequently fatal bone marrow stem cell cancer characterized by unbridled proliferation of malignant marrow stem cells with associated infection, anemia, and bleeding. An improved understanding of pathophysiology, improvements in measurement technology and at least 10 recently approved therapies have led to revamping the diagnostic, prognostic, and therapeutic landscape of AML.
One updated and one new classification system were published in 2022, both emphasizing the integration of molecular analysis into daily practice. Differences between the International Consensus Classification and major revisions from the previous 2016 WHO system provide both challenges and opportunities for care and clinical research.
The European Leukemia Net 2022 risk classification integrates knowledge from novel molecular findings and recent trial results, as well as emphasizing dynamic risk based on serial measurable residual disease assessment. However, how to leverage our burgeoning ability to measure a small number of potentially malignant myeloid cells into therapeutic decision making is controversial.
The diagnostic and therapeutic complexity plus the availability of newly approved agents requires a nuanced therapeutic algorithm which should integrate patient goals of care, comorbidities, and disease characteristics including the specific mutational profile of the patient's AML. The framework we suggest only represents the beginning of the discussion.
急性髓系白血病(AML)是一种常见的致命性骨髓干细胞癌,其特征是恶性骨髓干细胞不受控制地增殖,并伴有感染、贫血和出血。对病理生理学的认识不断提高,测量技术的改进以及至少 10 种最近批准的治疗方法,使得 AML 的诊断、预后和治疗领域发生了彻底改变。
2022 年发布了一个更新的和一个新的分类系统,两者都强调将分子分析纳入日常实践。国际共识分类与之前 2016 年世卫组织系统的主要修订之间的差异,为护理和临床研究既带来了挑战,也带来了机遇。
欧洲白血病网 2022 年风险分类整合了来自新的分子发现和最近试验结果的知识,以及强调基于连续可测量残留疾病评估的动态风险。然而,如何利用我们日益增长的能力将少量潜在恶性髓样细胞测量结果转化为治疗决策,仍存在争议。
诊断和治疗的复杂性加上新批准药物的可用性,需要一种细致的治疗算法,该算法应整合患者的护理目标、合并症和疾病特征,包括患者 AML 的特定突变特征。我们建议的框架仅代表讨论的开始。