Evidence map›Paper›PMID 19895223›Full record

Trial reportExpert review of molecular diagnostics2009

GUCY2C reverse transcriptase PCR to stage pN0 colorectal cancer patients.

Alex Mejia, Stephanie Schulz, Terry Hyslop, David S Weinberg, Scott A Waldman

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Expert review of molecular diagnostics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. GUCY2C as a biomarker to target precision therapies for patients with colorectal cancer.Expert review of precision medicine and drug development · 2021
    Article
  3. Article
  4. Article
  5. Review
  6. Molecular staging individualizing cancer management.Journal of surgical oncology · 2012
    Review
  7. Review
  8. Article
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 2 institutions in 1 country.

Alex MejiaDepartment of Pharmacology and Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Stephanie Schulz
Terry Hyslop
David S Weinberg
Scott A Waldman
Thomas Jefferson University · USFox Chase Cancer Center · US

Funding

CLINICAL PHARMACOLOGY TRAINING PROGRAMT32GM008562 · NIGMS · THOMAS JEFFERSON UNIVERSITY · PI WALTER K KRAFT, Scott A. Waldman · 1995 to 2026
$10.2M
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
Training Program in Human InvestigationK30RR022299 · NCRR · THOMAS JEFFERSON UNIVERSITY · PI WALDMAN, SCOTT A · 2005 to 2009
$1.5M
TRAINING PROGRAM IN HUMAN INVESTIGATIONK30HL004522 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI WALDMAN, SCOTT A. · 2000 to 2004
$964k
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 CA75123NCI NIH HHS CA95026NCI NIH HHS R01 CA075123NCI NIH HHS R01 CA095026NCI NIH HHS R21 CA112147NCI NIH HHS R33 CA112147NCRR NIH HHS K30 RR022299NHLBI NIH HHS K30 HL004522NIGMS NIH HHS T32 GM008562NIGMS NIH HHS T32 GM08562
6 · The paper itself

Abstract

The most important prognostic marker of survival and predictive marker of response to adjuvant chemotherapy in colon cancer patients is tumor cells in regional lymph nodes. Despite their importance, standard techniques to assess nodal metastases remain imperfect, as approximately 30% of patients with histology-negative lymph nodes (pN0) die of recurrent disease, reflecting occult metastases that escape detection. These observations highlight the clinical need for novel, accurate approaches to detect occult lymph node metastases in patients with colon cancer. GUCY2C is a biomarker whose expression normally is restricted to intestinal cells, but is near universally overexpressed by colorectal cancer cells. Recently, a prospective, multicenter, blinded clinical trial demonstrated for the first time that the prognostic utility of GUCY2C quantitative reverse transcriptase (qRT)-PCR to detect occult lymph node metastases in pN0 colorectal cancer patients. Molecular staging revealed that approximately 13% of pN0 patients were free of tumor cells, while approximately 87% had GUCY2C results that suggested occult metastases. The presence of occult lymph node metastases was the strongest independent predictor of time to recurrence and disease-free survival. These observations establish the utility of molecular detection of occult lymph node metastases for estimating prognostic risk in pN0 colorectal cancer patients. Advancing this molecular diagnostic into staging paradigms in clinical laboratories will require validation in independent patient populations, definition of the relationship between the quantity of occult tumor metastases and risk, and determination of the utility of GUCY2C qRT-PCR to identify pN0 patients who might benefit from adjuvant chemotherapy.

Indexed as

Biomarkers, TumorChemotherapy, AdjuvantColorectal NeoplasmsGuanylate CyclaseHumansLymphatic MetastasisNeoplasm StagingPathology, MolecularPrognosisProspective StudiesReceptors, EnterotoxinReceptors, Guanylate Cyclase-CoupledReceptors, PeptideReproducibility of ResultsReverse Transcriptase Polymerase Chain ReactionBiomarkers, TumorGuanylate CyclaseGUCY2C protein, humanReceptors, EnterotoxinReceptors, Guanylate Cyclase-CoupledReceptors, Peptide

Identifiers

PMID19895223
PMCPMC2810399
OpenAlexW2007608147

What OpenQuestion holds

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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.