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PMID: 15908663 Published · ppublish English Comparative Study Historical Article Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Molecular staging for survival prediction of colorectal cancer patients.

Eschrich S, Yang I, Bloom G, Kwong KY, Boulware D, Cantor A, Coppola D, Kruhøffer M, Aaltonen L, Orntoft TF, Quackenbush J, Yeatman TJ

Abstract

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. 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. 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. These data support further evaluation of molecular staging to discriminate good from poor prognosis patients, with the potential to direct adjuvant therapy.

MeSH Terms
Adult Cohort Studies Colorectal Neoplasms/genetics,mortality,pathology,therapy Combined Modality Therapy DNA Fingerprinting DNA, Complementary/analysis Female Genes, DCC History, 18th Century Humans Male Middle Aged Molecular Biology Neoplasm Staging/methods Oligonucleotide Array Sequence Analysis Predictive Value of Tests Probability Prognosis Risk Assessment Sensitivity and Specificity Statistics, Nonparametric Survival Analysis Tumor Suppressor Proteins/genetics
Chemicals
DNA, Complementary Tumor Suppressor Proteins
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Eschrich Steven
Department of Surgery, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
Yang Ivana
Bloom Greg
Kwong Ka Yin
Boulware David
Cantor Alan
Coppola Domenico
Kruhøffer Mogens
Aaltonen Lauri
Orntoft Torben F
Quackenbush John
Yeatman Timothy J
Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
0732-183X
Published
2005-05-20
Pages
3526-35
Language
English
Region
United States
NLM ID
8309333
Subset
IM
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