Acute myeloid leukemia: 2023 update on diagnosis, risk-stratification, and management

被引:204
|
作者
Shimony, Shai [1 ,2 ,3 ]
Stahl, Maximilian [1 ]
Stone, Richard M. [1 ,4 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA USA
[2] Tel Aviv Univ, Rabin Med Ctr, Tel Aviv, Israel
[3] Tel Aviv Univ, Fac Med, Tel Aviv, Israel
[4] Dana Farber Canc Inst, 450 Brookline Ave, Boston, MA 02215 USA
关键词
MINIMAL RESIDUAL DISEASE; ACUTE PROMYELOCYTIC LEUKEMIA; 1ST COMPLETE REMISSION; HEMATOPOIETIC-CELL TRANSPLANTATION; TRANS-RETINOIC ACID; HEALTH-ORGANIZATION CLASSIFICATION; RECEIVING INDUCTION CHEMOTHERAPY; PLUS INTENSIVE CHEMOTHERAPY; INDIVIDUAL PATIENT DATA; HIGH-DOSE DAUNORUBICIN;
D O I
10.1002/ajh.26822
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Disease overview: 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. Diagnosis: 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. Risk assessment and monitoring: 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. Risk adapted therapy: 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.
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页码:502 / 526
页数:25
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