MLL Munich Leukemia Laboratory, Munich, Germany.
J Clin Oncol. 2010 May 20;28(15):2529-37. doi: 10.1200/JCO.2009.23.4732. Epub 2010 Apr 20.
The Microarray Innovations in Leukemia study assessed the clinical utility of gene expression profiling as a single test to subtype leukemias into conventional categories of myeloid and lymphoid malignancies.
The investigation was performed in 11 laboratories across three continents and included 3,334 patients. An exploratory retrospective stage I study was designed for biomarker discovery and generated whole-genome expression profiles from 2,143 patients with leukemias and myelodysplastic syndromes. The gene expression profiling-based diagnostic accuracy was further validated in a prospective second study stage of an independent cohort of 1,191 patients.
On the basis of 2,096 samples, the stage I study achieved 92.2% classification accuracy for all 18 distinct classes investigated (median specificity of 99.7%). In a second cohort of 1,152 prospectively collected patients, a classification scheme reached 95.6% median sensitivity and 99.8% median specificity for 14 standard subtypes of acute leukemia (eight acute lymphoblastic leukemia and six acute myeloid leukemia classes, n = 693). In 29 (57%) of 51 discrepant cases, the microarray results had outperformed routine diagnostic methods.
Gene expression profiling is a robust technology for the diagnosis of hematologic malignancies with high accuracy. It may complement current diagnostic algorithms and could offer a reliable platform for patients who lack access to today's state-of-the-art diagnostic work-up. Our comprehensive gene expression data set will be submitted to the public domain to foster research focusing on the molecular understanding of leukemias.
白血病的微阵列创新研究评估了基因表达谱作为一种单一测试将白血病分为髓系和淋巴恶性肿瘤的常规分类的临床效用。
该研究在三大洲的 11 个实验室进行,共纳入 3334 名患者。设计了一项探索性回顾性 I 期研究,用于发现生物标志物,并从 2143 名白血病和骨髓增生异常综合征患者中生成全基因组表达谱。基于基因表达谱的诊断准确性在独立队列的 1191 名患者的前瞻性第二研究阶段中进一步得到验证。
基于 2096 个样本,I 期研究实现了所有 18 个不同分类的 92.2%分类准确性(中位数特异性为 99.7%)。在第二个 1152 名前瞻性采集的患者队列中,分类方案达到了 95.6%的中位数敏感性和 99.8%的中位数特异性,用于 14 种标准的急性白血病亚型(8 种急性淋巴细胞白血病和 6 种急性髓细胞白血病类别,n=693)。在 51 个不一致病例中的 29 个(57%)中,微阵列结果表现优于常规诊断方法。
基因表达谱是一种用于诊断血液恶性肿瘤的强大技术,具有很高的准确性。它可以补充当前的诊断算法,并为那些无法获得当今最先进诊断方法的患者提供可靠的平台。我们的综合基因表达数据集将提交给公共领域,以促进专注于白血病分子理解的研究。