Stanford University Medical Center, Dept of Pathology, Stanford, CA 94305, USA.
Am J Clin Pathol. 2013 Jun;139(6):818-25. doi: 10.1309/AJCP59WKRZVNHETN.
The classification of acute myeloid leukemia (AML) has evolved to the most recent World Health Organization (WHO) schema, which integrates genetic, morphologic, and prognostic data into a single system. However, this system was devised using adult data and how this system applies to a pediatric cohort is unknown. Performing a retrospective chart review, we examined our single-center experience with AML in 115 children and classified their leukemia using the WHO 2008 schema. We examined patient samples for mutations of FLT3, NPM1, and CEBPA. Overall survival was calculated within categories. In our pediatric population, most cases of AML had recurrent genetic abnormalities of favorable prognosis. More than 10% of patients in our series were categorized as AML, with myelodysplasia-related changes, an entity not well-described in pediatric patients. In addition, a large proportion of patients were categorized with secondary, therapy-related AML. To our knowledge, this is the first application of the WHO 2008 classification to a pediatric cohort. In comparison to adult studies, AML in the pediatric population shows a distinct distribution within the WHO 2008 classification.
急性髓系白血病(AML)的分类已经发展到最新的世界卫生组织(WHO)方案,该方案将遗传、形态和预后数据整合到一个单一的系统中。然而,该系统是使用成人数据设计的,其在儿科患者中的应用尚不清楚。我们进行了回顾性图表审查,检查了我们在 115 名儿童中使用 AML 的单中心经验,并使用 WHO 2008 方案对他们的白血病进行了分类。我们检查了患者样本中 FLT3、NPM1 和 CEBPA 的突变情况。在各个类别中计算了总生存率。在我们的儿科人群中,大多数 AML 病例具有有利预后的复发性遗传异常。我们系列中的超过 10%的患者被归类为 AML,伴骨髓增生异常相关改变,这在儿科患者中描述不多。此外,很大一部分患者被归类为继发性、治疗相关的 AML。据我们所知,这是 WHO 2008 分类首次应用于儿科患者。与成人研究相比,儿科人群中的 AML 在 WHO 2008 分类中有明显的分布差异。