Prediction of clinical outcome using gene expression profiling and artificial neural networks for patients with neuroblastoma

被引:151
作者
Wei, JS
Greer, BT
Westermann, F
Steinberg, SM
Son, CG
Chen, QR
Whiteford, CC
Bilke, S
Krasnoselsky, AL
Cenacchi, N
Catchpoole, D
Berthold, F
Schwab, M
Khan, J
机构
[1] NCI, Oncogenet Sect, Pediat Oncol Branch, Adv Technol Ctr,NIH, Gaithersburg, MD 20877 USA
[2] German Canc Res Ctr, Dept Tumour Genet B030, Heidelberg, Germany
[3] NCI, Ctr Canc Res, Biostat & Data Management Sect, NIH, Bethesda, MD USA
[4] Daejeon Univ, Coll Oriental Med, Dept Internal Med, Taejon, South Korea
[5] Childrens Hosp, Tumour Bank, Westmead, NSW, Australia
[6] Univ Cologne, Klin Kinderheilkunde, Dept Pediat, Cologne, Germany
关键词
D O I
10.1158/0008-5472.CAN-04-0695
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Currently, patients with neuroblastoma are classified into risk groups (e.g., according to the Children's Oncology Group risk-stratification) to guide physicians in the choice of the most appropriate therapy. Despite this careful stratification, the survival rate for patients with high-risk neuroblastoma remains <30%, and it is not possible to predict which of these high-risk patients will survive or succumb to the disease. Therefore, we have performed gene expression profiling using cDNA microarrays containing 42,578 clones and used artificial neural networks to develop an accurate predictor of survival for each individual patient with neuroblastoma. Using principal component analysis we found that neuroblastoma tumors exhibited inherent prognostic specific gene expression profiles. Subsequent artificial neural network-based prognosis prediction using expression levels of all 37,920 good-quality clones achieved 88% accuracy. Moreover, using an artificial neural network-based gene minimization strategy in a separate analysis we identified 19 genes, including 2 prognostic markers reported previously, MYCN and CD44, which correctly predicted outcome for 98% of these patients. In addition, these 19 predictor genes were able to additionally partition Children's Oncology Group-stratified high-risk patients into two subgroups according to their survival status (P = 0.0005). Our findings provide evidence of a gene expression signature that can predict prognosis independent of currently known risk factors and could assist physicians in the individual management of patients with high-risk neuroblastoma.
引用
收藏
页码:6883 / 6891
页数:9
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