Conneely Shannon E, Stevens Alexandra M
Department of Pediatric Hematology/Oncology, Texas Children's Cancer Center, Baylor College of Medicine, Fannin Street, Houston, TX 77030, USA.
Children (Basel). 2020 Feb 2;7(2):11. doi: 10.3390/children7020011.
Acute promyelocytic leukemia (APL) is a rare disease accounting for only 5%-10% of pediatric acute myeloid leukemia (AML) and fewer than 1000 cases occur annually in the United States across all age groups. Characterized by t (15; 17), with a resultant gene fusion driving leukemia development, advances in therapy have improved outcomes for APL significantly in the past several decades, now making APL the most curable form of AML in both children and adults. Cure rates in APL are now comparable to pediatric B-lymphoid leukemias. The success of APL treatment is due, in part, to the breadth of understanding of the driver mutation as well as collaborative efforts to quickly introduce and maximize the benefit of new therapies. Here, we review the presentation, clinical features, pathogenesis, and treatment advances in pediatric APL.
急性早幼粒细胞白血病(APL)是一种罕见疾病,仅占儿童急性髓系白血病(AML)的5%-10%,在美国所有年龄组中,每年发病例数少于1000例。其特征为t(15;17),由此产生的基因融合驱动白血病发展。在过去几十年中,治疗方面的进展显著改善了APL的治疗效果,现在APL已成为儿童和成人AML中最可治愈的形式。APL的治愈率现在与儿童B淋巴细胞白血病相当。APL治疗的成功部分归功于对驱动突变的广泛了解,以及迅速引入新疗法并使其效益最大化的合作努力。在此,我们综述儿童APL的临床表现、临床特征、发病机制及治疗进展。