Literature DB >> 23595092

Qualitative and quantitative issues of lymph nodes as prognostic factor in colon cancer.

Torhild Veen1, Bjørn S Nedrebø, Kjartan Stormark, Jon Arne Søreide, Hartwig Kørner, Kjetil Søreide.   

Abstract

For patients undergoing curative resections for colon cancer, the nodal status represents the strongest prognostic factor, yet at the same time the most disputed issue as well. Consequently, the qualitative and quantitative aspects of lymph node evaluation are thus being scrutinized beyond the blunt distinction between 'node positive' (pN+) and 'node negative' (pN0) disease. Controversy ranges from a minimal or 'least-unit' strategy as exemplified by the 'sentinel node' to a maximally invasive or 'all inclusive' approach by extensive surgery. Ranging between these two extremes of node sampling strategies are factors of quantitative and qualitative value, which may be subject to modification. Qualitative issues may include aspects of lymph node harvest reflected by surgeon, pathologist and even hospital performance, which all may be subject to modification. However, patient's age, gender and genotype may be non-modifiable, yet influence node sample. Quantitative issues may reflect the balance between absolute numbers and models investigating the relationships of positive to negative nodes (lymph node ratio; log odds of positive lymph nodes). This review provides an updated overview of the current controversies and a state-of-the-art perspective on the qualitative and quantitative aspects of using lymph nodes as a prognostic marker in colon cancer.
Copyright © 2013 S. Karger AG, Basel.

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Year:  2013        PMID: 23595092     DOI: 10.1159/000349923

Source DB:  PubMed          Journal:  Dig Surg        ISSN: 0253-4886            Impact factor:   2.588


  15 in total

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4.  The Log Odds of Positive Lymph Nodes Stratifies and Predicts Survival of High-Risk Individuals Among Stage III Rectal Cancer Patients.

Authors:  Christina W Lee; Katheryn H Wilkinson; Adam C Sheka; Glen E Leverson; Gregory D Kennedy
Journal:  Oncologist       Date:  2016-03-14

5.  The prognostic yield of biomarkers harvested in chemotherapy-naive stage II colon cancer: can we separate the wheat from the chaff?

Authors:  Martin M Watson; Kjetil Søreide
Journal:  Mol Med       Date:  2016-05-04       Impact factor: 6.354

6.  Influence of microsatellite instability and KRAS and BRAF mutations on lymph node harvest in stage I-III colon cancers.

Authors:  Marianne Berg; Marianne Guriby; Oddmund Nordgård; Bjørn S Nedrebø; Terje C Ahlquist; Rune Smaaland; Satu Oltedal; Jon Arne Søreide; Hartwig Kørner; Ragnhild A Lothe; Kjetil Søreide
Journal:  Mol Med       Date:  2013-09-10       Impact factor: 6.354

7.  Molecular subtypes in stage II-III colon cancer defined by genomic instability: early recurrence-risk associated with a high copy-number variation and loss of RUNX3 and CDKN2A.

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8.  Assessment of clinically related outcomes and biomarker analysis for translational integration in colorectal cancer (ACROBATICC): study protocol for a population-based, consecutive cohort of surgically treated colorectal cancers and resected colorectal liver metastasis.

Authors:  Kjetil Søreide; Martin M Watson; Dordi Lea; Oddmund Nordgård; Jon Arne Søreide; Hanne R Hagland
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9.  Long-Term Follow-Up and Survivorship After Completing Systematic Surveillance in Stage I-III Colorectal Cancer: Who Is Still at Risk?

Authors:  T Veen; K Stormark; B S Nedrebø; M Berg; J A Søreide; H Kørner; Kjetil Søreide
Journal:  J Gastrointest Cancer       Date:  2015-09

10.  Elevated microsatellite alterations at selected tetranucleotides in early-stage colorectal cancers with and without high-frequency microsatellite instability: same, same but different?

Authors:  Martin M Watson; Dordi Lea; Emma Rewcastle; Hanne R Hagland; Kjetil Søreide
Journal:  Cancer Med       Date:  2016-04-06       Impact factor: 4.452

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