Journal Article
. 2005 May; 23(15):3526-35.
doi: 10.1200/JCO.2005.00.695.

Molecular staging for survival prediction of colorectal cancer patients

Steven Eschrich 1 Ivana Yang  Greg Bloom  Ka Yin Kwong  David Boulware  Alan Cantor  Domenico Coppola  Mogens Kruhøffer  Lauri Aaltonen  Torben F Orntoft  John Quackenbush  Timothy J Yeatman  
  • PMID: 15908663
  •     127 citations


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.

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Prognosis Prediction of Colorectal Cancer Using Gene Expression Profiles.
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Identification of a 13-gene-based classifier as a potential biomarker to predict the effects of fluorouracil-based chemotherapy in colorectal cancer.
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The effect of MTHFD2 on the proliferation and migration of colorectal cancer cell lines.
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Polymorphic variants INSIG2 rs6726538, HLA-DRB1 rs9272143, and GCNT1P5 rs7780883 contribute to the susceptibility of cervical cancer in the Bangladeshi women.
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