Brown Patrick
1Departments of Oncology and Pediatrics, Johns Hopkins University School of Medicine.
Hematology Am Soc Hematol Educ Program. 2013;2013:596-600. doi: 10.1182/asheducation-2013.1.596.
Leukemia in infants is rare but generates tremendous interest due to its aggressive clinical presentation in a uniquely vulnerable host, its poor response to current therapies, and its unique biology that is increasingly pointing the way toward novel therapeutic approaches. This review highlights the key clinical, pathologic, and epidemiologic features of infant leukemia, including the high frequency of mixed lineage leukemia (MLL) gene rearrangements. The state of the art with regard to current approaches to risk stratified treatment of infant leukemia in the major international cooperative groups is discussed. Finally, exciting recent discoveries elucidating the molecular biology of infant leukemia are reviewed and novel targeted therapeutic strategies, including FLT3 inhibition and modulation of aberrant epigenetic programs, are suggested.
婴儿白血病较为罕见,但因其在极为脆弱的宿主中呈现出侵袭性临床表现、对当前治疗反应不佳以及独特生物学特性(这一特性日益为新型治疗方法指明方向)而备受关注。本综述着重介绍婴儿白血病的关键临床、病理和流行病学特征,包括混合谱系白血病(MLL)基因重排的高频率。文中还讨论了主要国际合作组针对婴儿白血病进行风险分层治疗的当前方法的最新进展。最后,回顾了阐明婴儿白血病分子生物学的近期令人兴奋的发现,并提出了新型靶向治疗策略,包括FLT3抑制和异常表观遗传程序的调控。