Redefining high-risk patients with stage II colon cancer by risk index and microRNA-21: results from a population-based cohort
Background: The aim of the present study was to analyse the prognostic value of microRNA-21 (miRNA-21) in patients with stage II colon cancer aiming at a risk index for this group of patients. Methods: A population-based cohort of 554 patients was included. MicroRNA-21 was analysed by qPCR based on...
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Published in | British journal of cancer Vol. 111; no. 7; pp. 1285 - 1292 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
23.09.2014
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 0007-0920 1532-1827 1532-1827 |
DOI | 10.1038/bjc.2014.409 |
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Summary: | Background:
The aim of the present study was to analyse the prognostic value of microRNA-21 (miRNA-21) in patients with stage II colon cancer aiming at a risk index for this group of patients.
Methods:
A population-based cohort of 554 patients was included. MicroRNA-21 was analysed by qPCR based on tumour tissue. An index was created using the coefficients obtained from a collective multiple Cox regression. The entire procedure was cross-validated (10-fold). The performance of the index was quantified by time-dependent receiver operating characteristics curves.
Results:
High miRNA-21 expression was associated with an unfavourable recurrence-free cancer-specific survival (RF-CSS), hazard ratio 1.35 (95% confidence interval, 1.03–1.76) (
P
=0.028). The generated RF-CSS index divided the traditional high-risk patients into subgroups with 5-year RF-CSS rates of 87% and 73%, respectively (
P
<0.001). The overall survival (OS) index identified three different subgroups (
P
<0.001). Cross-validated 5-year OS rates were 88%, 68%, and 50%, respectively.
Conclusions:
This population-based study supports miRNA-21 as an additional prognostic biomarker in patients with stage II colon cancer. Furthermore, the introduction of a risk index may guide the use of postoperative adjuvant treatment in a more appropriate way compared with current practice. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 On behalf of Danish Colorectal Cancer Group (DCCG). |
ISSN: | 0007-0920 1532-1827 1532-1827 |
DOI: | 10.1038/bjc.2014.409 |