Evidence map›Paper›PMID 22252429›Full record

ArticleJournal of surgical oncology2012

Analytic lymph node number establishes staging accuracy by occult tumor burden in colorectal cancer.

Terry Hyslop, David S Weinberg, Stephanie Schulz, Alan Barkun, Scott A Waldman

Open access · greenAbstract read
In one paragraph

Article in Journal of surgical oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Identification of key lncRNAs as prognostic prediction models for colorectal cancer based on LASSO.International journal of clinical and experimental pathology · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Terry HyslopDepartment of Pharmacology and Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA 19107, USA.
David S Weinberg
Stephanie Schulz
Alan Barkun
Scott A Waldman
Thomas Jefferson University · USFox Chase Cancer Center · USMcGill University · CA

Funding

Guanylyl Cyclase C in Blood and Colorectal CancerR01CA095026 · NCI · THOMAS JEFFERSON UNIVERSITY · PI WALDMAN, SCOTT A · 2003 to 2008
$5.1M
GUANYLYL CYCLASE C AS A BIOMARKER FOR COLORECTAL CANCERR01CA075123 · NCI · THOMAS JEFFERSON UNIVERSITY · PI WALDMAN, SCOTT A. · 1998 to 2006
$5.1M
Occult lymph node metastases and racial disparities in colon cancer outcomesRC1CA146033 · NCI · THOMAS JEFFERSON UNIVERSITY · PI WALDMAN, SCOTT A · 2009 to 2010
$997k
Nonlinear Models of mRNA Expression in Cancer by RT-PCRR33CA112147 · NCI · THOMAS JEFFERSON UNIVERSITY · PI HYSLOP, TERRY · 2007 to 2009
$666k
Nonlinear Models of mRNA Expression in Cancer by RT-PCRR21CA112147 · NCI · THOMAS JEFFERSON UNIVERSITY · PI HYSLOP, TERRY · 2005 to 2005
$140k
NCI NIH HHS CA112147NCI NIH HHS CA146033NCI NIH HHS CA75123NCI NIH HHS CA95026NCI NIH HHS R01 CA075123NCI NIH HHS R01 CA095026NCI NIH HHS R21 CA112147NCI NIH HHS R33 CA112147NCI NIH HHS RC1 CA146033
6 · The paper itself

Abstract

BACKGROUND AND

objectivesRecurrence in lymph node-negative (pN0) colorectal cancer suggests the presence of undetected occult metastases. Occult tumor burden in nodes estimated by GUCY2C RT-qPCR predicts risk of disease recurrence. This study explored the impact of the number of nodes analyzed by RT-qPCR (analytic) on the prognostic utility of occult tumor burden.

methodsLymph nodes (range: 2-159) from 282 prospectively enrolled pN0 colorectal cancer patients, followed for a median of 24 months (range: 2-63), were analyzed by GUCY2C RT-qPCR. Prognostic risk categorization defined using occult tumor burden was the primary outcome measure. Association of prognostic variables and risk category were defined by multivariable polytomous and semi-parametric polytomous logistic regression.

resultsOccult tumor burden stratified this pN0 cohort into categories of low (60%; recurrence rate (RR) = 2.3% [95% CI 0.1-4.5%]), intermediate (31%; RR = 33.3% [23.7-44.1%]), and high (9%; RR = 68.0% [46.5-85.1%], P < 0.001) risk of recurrence. Beyond race and T stage, the number of analytic nodes was an independent marker of risk category (P < 0.001). When >12 nodes were analyzed, occult tumor burden almost completely resolved prognostic risk classification of pN0 patients.

conclusionsThe prognostic utility of occult tumor burden assessed by GUCY2C RT-qPCR is dependent on the number of analytic lymph nodes.

Indexed as

Tumor BurdenAdultAgedAged, 80 and overColorectal NeoplasmsFemaleHumansLogistic ModelsLymphatic MetastasisLymph NodesMaleMiddle AgedNeoplasm Recurrence, LocalNeoplasm StagingNeoplasms, Unknown PrimaryOdds Ratio

Identifiers

PMID22252429
PMCPMC3370134
OpenAlexW2060970222

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.