Sirulnik L Andres, Stone Richard M
Dept. of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, 44 Binney Street, Boston, MA 02116, USA.
Clin Adv Hematol Oncol. 2005 May;3(5):391-7, 429.
Acute promyelocytic leukemia (APL) is a distinct subtype of acute myeloid leukemia that comprises about 10% of cases. It is characterized by the accumulation of granulocytic cells blocked at the promyelocytic stage of differentiation in the bone marrow and the peripheral blood, life-threatening coagulopathy, and a remarkable response to treatment with all-trans-retinoic acid (ATRA), arsenic trioxide, and anthracyclines. Current treatment strategies with ATRA and anthracycline-based chemotherapy has dramatically transformed APL into the most curable of all acute leukemias. Advances in supportive care together with the early recognition of treatment-related complications have also contributed significantly to increased cure rates. In this review we explore current treatment strategies in the management of newly diagnosed APL. We also highlight practical points that may serve as a guideline for the treating physician and address current controversies in the choice of treatment.
急性早幼粒细胞白血病(APL)是急性髓系白血病的一种独特亚型,约占所有病例的10%。其特征是骨髓和外周血中处于早幼粒细胞分化阶段的粒细胞积聚、危及生命的凝血病,以及对全反式维甲酸(ATRA)、三氧化二砷和蒽环类药物治疗有显著反应。目前基于ATRA和蒽环类药物的化疗治疗策略已将APL显著转变为所有急性白血病中最可治愈的类型。支持治疗的进展以及对治疗相关并发症的早期识别也对治愈率的提高做出了重大贡献。在本综述中,我们探讨了新诊断APL治疗的当前策略。我们还强调了一些实用要点,这些要点可作为治疗医生的指导方针,并讨论了当前治疗选择中的争议。