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Redefining high-risk patients with stage II colon cancer by risk index and microRNA-21: results from a population-based cohort.
Hansen, T F; Kjær-Frifeldt, S; Christensen, R D; Morgenthaler, S; Blondal, T; Lindebjerg, J; Sørensen, F B; Jakobsen, A.
Afiliação
  • Hansen TF; 1] Department of Oncology, Vejle Hospital, part of Lillebaelt Hospital, Kabbeltoft 25, 7100 Vejle, Denmark [2] Institute of Regional Health Research, University of Southern Denmark, Odense, Denmark.
  • Kjær-Frifeldt S; 1] Institute of Regional Health Research, University of Southern Denmark, Odense, Denmark [2] Department of Clinical Pathology, Vejle Hospital, part of Lillebaelt Hospital, Vejle, Denmark.
  • Christensen RD; Research Unit of General Practice Odense, Institute of Public Health, University of Southern Denmark, Odense, Denmark.
  • Morgenthaler S; Exiqon A/S, Vedbæk, Denmark.
  • Blondal T; Exiqon A/S, Vedbæk, Denmark.
  • Lindebjerg J; Department of Clinical Pathology, Vejle Hospital, part of Lillebaelt Hospital, Vejle, Denmark.
  • Sørensen FB; 1] Institute of Regional Health Research, University of Southern Denmark, Odense, Denmark [2] Department of Clinical Pathology, Vejle Hospital, part of Lillebaelt Hospital, Vejle, Denmark.
  • Jakobsen A; 1] Department of Oncology, Vejle Hospital, part of Lillebaelt Hospital, Kabbeltoft 25, 7100 Vejle, Denmark [2] Institute of Regional Health Research, University of Southern Denmark, Odense, Denmark.
Br J Cancer ; 111(7): 1285-92, 2014 Sep 23.
Article em En | MEDLINE | ID: mdl-25051407
ABSTRACT

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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / MicroRNAs Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / MicroRNAs Idioma: En Ano de publicação: 2014 Tipo de documento: Article