Update on acute promyelocytic leukemia in the pediatric population

A. Ruiz-Rodriguez, Lucia ObandoMadrigal, Ana Lucia Mateus-Vargas
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Abstract

Acute promyelocytic leukemia (APL) has shown differences in incidence around the world, it has a characteristic molecular, pathogenic and clinical development mechanism. Despite being a low incidence acute myeloid leukemia (AML) compared to other AML and having a good response to therapy, it continues to be of interest due to the toxicities of its current treatment, to mutations that have shown resistance to those drugs, and to the few possibilities of alternative treatment with all-trans retinoic acid (ATRA) and anthracyclines in the pediatric population. Furthermore, the description of new mutations that originate APL produced by LPA generates new interest in studies that may shed light on their effects on the disease’s incidence, prognoses, and response to treatment. This article aims to review different studies that describe findings of APL in terms of incidences, treatments, side effects, survival, especially in the pediatric population. Different studies propose the use of ATRA - arsenic trioxide (ATO) as the first line of treatment, however, few have been carried out in the pediatric population and the use of ATO is not recommended in children under 5 years of age. On the other hand, the differentiation syndrome (DS) has been d
儿科人群急性早幼粒细胞白血病的最新进展
急性早幼粒细胞白血病(Acute promyelocytic leukemia, APL)在世界范围内发病率存在差异,具有独特的分子、致病和临床发展机制。尽管与其他AML相比,急性髓系白血病(AML)的发病率较低,并且对治疗有良好的反应,但由于其目前治疗的毒性,对这些药物产生耐药性的突变,以及在儿科人群中使用全反式维甲酸(ATRA)和蒽环类药物替代治疗的可能性很小,因此它继续受到关注。此外,对LPA产生的APL的新突变的描述引起了新的研究兴趣,这些研究可能会揭示它们对疾病发病率、预后和治疗反应的影响。本文旨在回顾不同的研究,从发病率、治疗、副作用、生存等方面描述APL的发现,特别是在儿科人群中。不同的研究建议使用ATRA -三氧化二砷(ATO)作为一线治疗,然而,很少在儿科人群中进行,并且不建议在5岁以下儿童中使用ATO。另一方面,辨证论治(DS)已被证实
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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