An update of current treatments for adult acute myeloid leukemia

被引:427
|
作者
Dombret, Herve [1 ,2 ]
Gardin, Claude [2 ,3 ]
机构
[1] Hop St Louis, AP HP, Dept Hematol, Paris, France
[2] Univ Paris Diderot, Inst Univ Hematol, Leukemia Translat Lab, EA3518, Paris, France
[3] Hop Avicenne, AP HP, Dept Hematol, F-93009 Bobigny, France
关键词
MINIMAL RESIDUAL DISEASE; HIGH-DOSE CYTARABINE; TRANS-RETINOIC ACID; STEM-CELL TRANSPLANTATION; RISK MYELODYSPLASTIC SYNDROME; 1ST COMPLETE REMISSION; PHASE-III TRIAL; OLDER PATIENTS; GEMTUZUMAB OZOGAMICIN; ARSENIC TRIOXIDE;
D O I
10.1182/blood-2015-08-604520
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recent advances in acute myeloid leukemia (AML) biology and its genetic landscape should ultimately lead to more subset-specific AML therapies, ideally tailored to each patient's disease. Although a growing number of distinct AML subsets have been increasingly characterized, patient management has remained disappointingly uniform. If one excludes acute promyelocytic leukemia, current AML management still relies largely on intensive chemotherapy and allogeneic hematopoietic stem cell transplantation (HSCT), at least in younger patients who can tolerate such intensive treatments. Nevertheless, progress has been made, notably in terms of standard drug dose intensification and safer allogeneic HSCT procedures, allowing a larger proportion of patients to achieve durable remission. In addition, improved identification of patients at relatively low risk of relapse should limit their undue exposure to the risks of HSCT in first remission. The role of new effective agents, such as purine analogs or gemtuzumab ozogamicin, is still under investigation, whereas promising new targeted agents are under clinical development. In contrast, minimal advances have been made for patients unable to tolerate intensive treatment, mostly representing older patients. The availability of hypomethylating agents likely represents an encouraging first step for this latter population, and it is hoped will allow for more efficient combinations with novel agents.
引用
收藏
页码:53 / 61
页数:9
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