Andersson A, Ritz C, Lindgren D, Edén P, Lassen C, Heldrup J, Olofsson T, Råde J, Fontes M, Porwit-Macdonald A, Behrendtz M, Höglund M, Johansson B, Fioretos T
Department of Clinical Genetics, Lund University Hospital, Lund, Sweden.
Leukemia. 2007 Jun;21(6):1198-203. doi: 10.1038/sj.leu.2404688. Epub 2007 Apr 5.
Gene expression analyses were performed on 121 consecutive childhood leukemias (87 B-lineage acute lymphoblastic leukemias (ALLs), 11 T-cell ALLs and 23 acute myeloid leukemias (AMLs)), investigated during an 8-year period at a single center. The supervised learning algorithm k-nearest neighbor was utilized to build gene expression predictors that could classify the ALLs/AMLs according to clinically important subtypes with high accuracy. Validation experiments in an independent data set verified the high prediction accuracies of our classifiers. B-lineage ALLs with uncharacteristic cytogenetic aberrations or with a normal karyotype displayed heterogeneous gene expression profiles, resulting in low prediction accuracies. Minimal residual disease status (MRD) in T-cell ALLs with a high (>0.1%) MRD at day 29 could be classified with 100% accuracy already at the time of diagnosis. In pediatric leukemias with uncharacteristic cytogenetic aberrations or with a normal karyotype, unsupervised analysis identified two novel subgroups: one consisting mainly of cases remaining in complete remission (CR) and one containing a few patients in CR and all but one of the patients who relapsed. This study of a consecutive series of childhood leukemias confirms and extends further previous reports demonstrating that global gene expression profiling provides a valuable tool for genetic and clinical classification of childhood leukemias.
对在一个中心8年期间研究的121例连续性儿童白血病(87例B系急性淋巴细胞白血病(ALL)、11例T细胞ALL和23例急性髓细胞白血病(AML))进行了基因表达分析。利用监督学习算法k近邻构建基因表达预测模型,该模型可根据临床重要亚型对ALL/AML进行高精度分类。在独立数据集中的验证实验证实了我们分类器的高预测准确性。具有非典型细胞遗传学异常或正常核型的B系ALL显示出异质性基因表达谱,导致预测准确性较低。在第29天微小残留病状态(MRD)高(>0.1%)的T细胞ALL中,在诊断时即可100%准确分类。在具有非典型细胞遗传学异常或正常核型的儿童白血病中,无监督分析识别出两个新亚组:一个主要由持续完全缓解(CR)的病例组成,另一个包含少数处于CR的患者以及除一名复发患者外的所有复发患者。这项对一系列连续性儿童白血病的研究证实并进一步扩展了先前的报告,表明全基因组表达谱分析为儿童白血病的遗传和临床分类提供了一个有价值的工具。