Clinical Utility of Microarray-Based Gene Expression Profiling in the Diagnosis and Subclassification of Leukemia: Report From the International Microarray Innovations in Leukemia Study Group

被引:514
作者
Haferlach, Torsten
Kohlmann, Alexander
Wieczorek, Lothar
Basso, Giuseppe
Kronnie, Geertruy Te
Bene, Marie-Christine
De Vos, John
Hernandez, Jesus M.
Hofmann, Wolf-Karsten
Mills, Ken I.
Gilkes, Amanda
Chiaretti, Sabina
Shurtleff, Sheila A.
Kipps, Thomas J.
Rassenti, Laura Z.
Yeoh, Allen E.
Papenhausen, Peter R.
Liu, Wei-min
Williams, P. Mickey
Foa, Robin
机构
[1] MLL Munich Leukemia Lab, Munich, Germany
[2] Univ Hosp Benjamin Franklin, Charite, Dept Hematol & Oncol, Berlin, Germany
[3] Univ Padua, Lab Ematol & Oncol Pediat, Padua, Italy
[4] Univ Roma La Sapienza, Div Hematol, Rome, Italy
[5] Hop St Eloi, CHU Montpellier, Inst Rech Biotherapie, Montpellier, France
[6] Univ Salamanca, CSIC, Ctr Invest Canc, Inst Biol Mol & Celular Canc, E-37008 Salamanca, Spain
[7] Cardiff Univ, Sch Med, Dept Haematol, Cardiff, S Glam, Wales
[8] Natl Univ Singapore, Singapore 117548, Singapore
[9] Roche Mol Syst, Pleasanton, CA USA
[10] Univ Calif San Diego, Moores Canc Ctr, San Diego, CA 92103 USA
[11] St Jude Childrens Res Hosp, Dept Pathol, Memphis, TN 38105 USA
[12] Lab Corp Amer, Dept Pediat, Res Triangle Pk, NC USA
[13] Lab Corp Amer, Dept Pathol, Res Triangle Pk, NC USA
关键词
ACUTE MYELOID-LEUKEMIA; ACUTE LYMPHOBLASTIC-LEUKEMIA; MINIMAL RESIDUAL DISEASE; NORMAL KARYOTYPE; MUTATIONS; CANCER; ADULT; CLASSIFICATION; SIGNATURES; SURVIVAL;
D O I
10.1200/JCO.2009.23.4732
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose 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. Methods 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. Results 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. Conclusion 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.
引用
收藏
页码:2529 / 2537
页数:9
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