Evidence map›Paper›PMID 29511559›Full record

ArticleUnited European gastroenterology journal2018

Genetic Biopsy for Prediction of Surveillance Intervals after Endoscopic Resection of Colonic Polyps: Results of the GENESIS Study.

Andreas W Berger, Katja Raedler, Cord Langner, Leopold Ludwig, Nektarios Dikopoulos, Karl F Becker, Julia Slotta-Huspenina, Michael Quante, Daniel Schwerdel, Lukas Perkhofer and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in United European gastroenterology journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  4. 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

15 authors at 4 institutions in 2 countries.

Andreas W BergerClinic for Internal Medicine I, Ulm University, Ulm, Germany.
Katja RaedlerClinic for Internal Medicine I, Ulm University, Ulm, Germany.
Cord LangnerInstitute for Pathology, Medical University Graz, Graz, Austria.
Leopold LudwigOutpatient Clinic for Gastroenterology, Dornstadt, Germany.
Nektarios DikopoulosOutpatient Clinic for Gastroenterology, Dornstadt, Germany.
Karl F BeckerInstitute for General Pathology and Pathological Anatomy, Technical University Munich, Munich, Germany.
Julia Slotta-HuspeninaInstitute for General Pathology and Pathological Anatomy, Technical University Munich, Munich, Germany.
Michael QuanteDepartment of Internal Medicine, Technical University Munich, Munich, Germany.
Daniel SchwerdelClinic for Internal Medicine I, Ulm University, Ulm, Germany.
Lukas PerkhoferClinic for Internal Medicine I, Ulm University, Ulm, Germany.
Alexander KlegerClinic for Internal Medicine I, Ulm University, Ulm, Germany.
Eugen ZizerClinic for Internal Medicine I, Ulm University, Ulm, Germany.
Franz OswaldClinic for Internal Medicine I, Ulm University, Ulm, Germany.
Thomas SeufferleinClinic for Internal Medicine I, Ulm University, Ulm, Germany.
Alexander MeiningClinic for Internal Medicine I, Ulm University, Ulm, Germany.
Universität Ulm · DETechnical University of Munich · DEForschungsinstitut für Kinderernährung · DEMedical University of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveCurrent surveillance strategies for colorectal cancer following polypectomy are determined by endoscopic and histopathological factors. Such a distinction has been challenged. The present study was designed to identify molecular parameters in colonic polyps potentially defining new sub-groups at risk.

methodsOne hundred patients were enrolled in this multicentre study. Polyps biopsies underwent formalin-free processing (PAXgene, PreAnalytiX) and targeted next generation sequencing (38 genes (QIAGEN), NextSeq 500 platform (Illumina)). Genetic and histopathological analyses were done blinded to other data.

resultsIn 100 patients, 224 polyps were removed. Significant associations of genetic alterations with endoscopic or histological polyp characteristics were observed for

conclusionsAssessment of the mutational landscape of polyps can be integrated in the workflow of current colonoscopy practice. There are distinct genetic patterns related to polyp size and location. These results suffice to optimise individual risk calculation and may help to better define surveillance intervals.

Indexed as

colorectal cancerColorectal polypsgeneticspolypectomysurveillance

Identifiers

PMID29511559
PMCPMC5833231
OpenAlexW2740782163

What OpenQuestion holds

Textmetadata
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.