Molecular staging for survival prediction of colorectal cancer patients

被引:275
作者
Eschrich, S
Yang, I
Bloom, G
Kwong, KY
Boulware, D
Cantor, A
Coppola, D
Kruhoffer, M
Aaltonen, L
Orntoft, TF
Quackenbush, J
Yeatman, TJ
机构
[1] H Lee Moffit Canc Ctr & Res Inst, Dept Surg, Tampa, FL 33612 USA
[2] H Lee Moffit Canc Ctr & Res Inst, Dept Pathol, Tampa, FL 33612 USA
[3] H Lee Moffit Canc Ctr & Res Inst, Dept Biostat, Tampa, FL 33612 USA
[4] Inst Genom Res, Rockville, MD USA
[5] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Stat, Baltimore, MD USA
[6] George Washington Univ, Dept Biochem, Washington, DC USA
[7] Aarhus Univ Hosp, Dept Clin Biochem, Mol Diagnost Lab, Skejby, Denmark
[8] Biomedicum, Dept Med Genet, Helsinki, Finland
关键词
D O I
10.1200/JCO.2005.00.695
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose The Dukes' staging system is the gold standard for predicting colorectal cancer prognosis; however, accurate classification of intermediate-stage cases is problematic. We hypothesized that molecular fingerprints could provide more accurate staging and potentially assist in directing adjuvant therapy. Methods A 32,000 cDNA microarray was used to evaluate 78 human colon cancer specimens, and these results were correlated with survival. Molecular classifiers were produced to predict outcome. Results Molecular staging, based on 43 core genes, was 90% accurate (93% sensitivity, 84% specificity) in predicting 36-month overall survival in 78 patients. This result was significantly better than Dukes' staging (P = 03878), discriminated patients into significantly different groups by survival time (P < .001, log-rank test), and was significantly different from chance (P < .001, 1,000 permutations). Furthermore, the classifier was able to discriminate a survival difference in an independent test set from Denmark. Molecular staging identifies patient prognosis (as represented by 36-month survival) more accurately than the traditional clinical staging, particularly for intermediate Dukes' stage B and C patients. The classifier was based on a core set of 43 genes, including osteopontin and neuregulin, which have biologic significance for this disease. Conclusion These data support further evaluation of molecular staging to discriminate good from poor prognosis -patients, with the potential to direct adjuvant therapy. (c) 2005 by American Society of Clinical Oncology.
引用
收藏
页码:3526 / 3535
页数:10
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