Iland Harry J, Wei Andrew, Seymour John F
Institute of Haematology, Royal Prince Alfred Hospital, Missenden Road, Camperdown, NSW 2050, Australia; University of Sydney, Sydney, NSW 2006, Australia.
Department of Haematology, The Alfred Hospital, Commercial Road, Melbourne, VIC 3004, Australia; Monash University, Melbourne, VIC, Australia.
Best Pract Res Clin Haematol. 2014 Mar;27(1):39-52. doi: 10.1016/j.beha.2014.04.003. Epub 2014 Apr 12.
Until recently, the standard of care in the treatment of APL has involved the combination of all-trans retinoic acid with anthracycline-based chemotherapy during both induction and consolidation. Additionally, the intensity of consolidation chemotherapy has evolved according to a universally accepted relapse-risk stratification algorithm based on the white cell and platelet counts at presentation. That standard of care is being challenged by the increasing incorporation of arsenic trioxide into front-line treatment protocols, based on two complementary observations. The first is the undoubted anti-leukaemic activity of arsenic trioxide as shown in the relapsed and refractory setting, and in the initial management of low- and intermediate-risk patients. The second is an improved understanding of the action of both all-trans retinoic acid and arsenic trioxide in mediating APL cell eradication, with increasing recognition that PML-RARA fusion protein degradation rather than direct induction of terminal differentiation is the primary mechanism for their ability to eliminate leukaemia initiating cells. As a result, we believe the standard of care for initial therapy in APL is shifting towards an all-trans retinoic acid plus arsenic trioxide-based approach, with additional chemotherapy reserved for patients with high-risk disease.
直到最近,急性早幼粒细胞白血病(APL)的标准治疗方案在诱导和巩固治疗期间都涉及全反式维甲酸与蒽环类化疗药物的联合使用。此外,巩固化疗的强度已根据基于初诊时白细胞和血小板计数的普遍接受的复发风险分层算法而演变。基于两项互补的观察结果,三氧化二砷越来越多地被纳入一线治疗方案,这一标准治疗方案正受到挑战。首先是三氧化二砷在复发和难治性病例以及低风险和中风险患者的初始治疗中所显示出的毋庸置疑的抗白血病活性。其次是对全反式维甲酸和三氧化二砷在介导APL细胞清除中的作用有了更深入的了解,越来越认识到早幼粒细胞白血病/维甲酸受体α(PML-RARA)融合蛋白降解而非直接诱导终末分化是它们消除白血病起始细胞能力的主要机制。因此,我们认为APL初始治疗的标准治疗方案正在转向以全反式维甲酸加三氧化二砷为基础的方法,对于高危疾病患者则保留额外的化疗。