Department of Laboratory Medicine, Laboratory of Hematology, Radboudumc, Nijmegen, The Netherlands.
Department of Molecular Biology, Radboud University, Nijmegen, The Netherlands.
Ann Hematol. 2022 Mar;101(3):571-579. doi: 10.1007/s00277-021-04747-x. Epub 2022 Jan 13.
Acute myeloid leukemia (AML) is a highly heterogeneous disease showing dynamic clonal evolution patterns over time. Various subclones may be present simultaneously and subclones may show a different expansion pattern and respond differently to applied therapies. It is already clear that immunophenotyping and genetic analyses may yield overlapping, but also complementary information. Detailed information on the genetic make-up of immunophenotypically defined subclones is however scarce. We performed error-corrected sequencing for 27 myeloid leukemia driver genes in 86, FACS-sorted immunophenotypically characterized normal and aberrant subfractions in 10 AML patients. We identified three main scenarios. In the first group of patients, the two techniques were equally well characterizing the malignancy. In the second group, most of the isolated populations did not express aberrant immunophenotypes but still harbored several genetic aberrancies, indicating that the information obtained only by immunophenotyping would be incomplete. Vice versa, one patient was identified in which genetic mutations were found only in a small fraction of the immunophenotypically defined malignant populations, indicating that the genetic analysis gave an incomplete picture of the disease. We conclude that currently, characterization of leukemic cells in AML by molecular and immunophenotypic techniques is complementary, and infer that both techniques should be used in parallel in order to obtain the most complete view on the disease.
急性髓系白血病 (AML) 是一种高度异质性疾病,随着时间的推移表现出动态的克隆进化模式。各种亚克隆可能同时存在,并且亚克隆可能表现出不同的扩增模式,对应用的治疗方法反应不同。已经很清楚,免疫表型分析和遗传分析可能会产生重叠但互补的信息。然而,关于免疫表型定义的亚克隆的遗传构成的详细信息还很缺乏。我们对 10 名 AML 患者的 86 个经 FACS 分选的免疫表型特征正常和异常亚群进行了 27 个髓系白血病驱动基因的纠错测序。我们确定了三种主要情况。在第一组患者中,两种技术同样能够很好地描述恶性程度。在第二组中,大多数分离的群体没有表达异常的免疫表型,但仍然存在几种遗传异常,表明仅通过免疫表型获得的信息是不完整的。相反,在一名患者中,仅在免疫表型定义的恶性群体的一小部分中发现了基因突变,这表明遗传分析对疾病的描述不完整。我们得出的结论是,目前通过分子和免疫表型技术对 AML 中的白血病细胞进行特征描述是互补的,并推断为了获得对疾病最全面的了解,两种技术都应该并行使用。