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Advances in Pediatric Acute Promyelocytic Leukemia

机译:小儿急性早幼粒细胞白血病的研究进展

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摘要

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.
机译:急性早幼粒细胞白血病(APL)是一种罕见的疾病,仅占小儿急性髓细胞性白血病(AML)的5%–10%,在美国各个年龄段每年发生的病例不到1000例。以t(15; 17)为特征,伴随着基因融合促进白血病的发展,在过去的几十年中,治疗的进步显着改善了APL的疗效,现在使APL成为儿童和成人中最可治愈的AML形式。现在,APL的治愈率可与小儿B淋巴白血病相媲美。 APL治疗的成功部分归因于对驾驶员突变的理解广度以及为快速引入新疗法并使新疗法的利益最大化而进行的共同努力。在这里,我们回顾了儿科APL的表现,临床特征,发病机理和治疗进展。

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