Tallman Martin S
Department of Medicine, Northwestern University Feinberg School of Medicine, and Robert H Lurie Comprehensive Cancer Center, Chicago, IL 60611, USA.
Semin Hematol. 2004 Apr;41(2 Suppl 4):27-32. doi: 10.1053/j.seminhematol.2004.02.004.
Substantial progress has occurred in the treatment of acute promyelocytic leukemia (APL) because of improved understanding of the pathophysiology of the disease and identification of a molecular target. Novel agents such as all-trans retinoic acid (ATRA) (alone or combined with chemotherapy) and, more recently, arsenic trioxide have produced complete remission in most patients with newly diagnosed APL and/or relapsed or refractory disease, respectively. Use of these targeted therapies has resulted in evolution of the disease from one that was historically one of the most fatal subtypes of acute myeloid leukemia (AML) to one that appears curable in 70% to 80% of patients. The targeted approach to treatment of this disease can serve as a paradigm for the treatment of other leukemias.
由于对急性早幼粒细胞白血病(APL)病理生理学的深入了解以及分子靶点的确定,APL的治疗取得了重大进展。新型药物如全反式维甲酸(ATRA)(单独使用或与化疗联合使用),以及最近的三氧化二砷,分别使大多数新诊断的APL患者和/或复发或难治性疾病患者获得了完全缓解。这些靶向治疗的应用已使该疾病从历史上急性髓系白血病(AML)最致命的亚型之一,演变为一种在70%至80%的患者中似乎可治愈的疾病。这种疾病的靶向治疗方法可作为其他白血病治疗的范例。