Evidence map›Paper›PMID 24728704›Full record

ArticleVirchows Archiv : an international journal of pathology2014

Defined morphological criteria allow reliable diagnosis of colorectal serrated polyps and predict polyp genetics.

Tilman T Rau, Abbas Agaimy, Anastasia Gehoff, Carol Geppert, Klaus Jung, Katharina Knobloch, Cord Langner, Alessandro Lugli, Irene Groenbus-Lurkin, Iris D Nagtegaal and 7 more

Open access · bronzeAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Evolving pathologic concepts of serrated lesions of the colorectum.Journal of pathology and translational medicine · 2020
    Review
  5. Gastric and small intestinal traditional serrated adenomas: a detailed morphologic and immunohistochemical analysis.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2020
    Article
  6. Molecular Biomarkers of Sessile Serrated Adenoma/Polyps.Clinical and translational gastroenterology · 2019
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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

17 authors at 11 institutions in 5 countries.

Tilman T RauInstitute of Pathology, Friedrich Alexander Universität Erlangen-Nürnberg, Krankenhausstraße 8-10, 91054, Erlangen, Germany, Tilman.Rau@uk-erlangen.de.
Abbas Agaimy
Anastasia Gehoff
Carol Geppert
Klaus Jung
Katharina Knobloch
Cord Langner
Alessandro Lugli
Irene Groenbus-Lurkin
Iris D Nagtegaal
Josef Rüschoff
Xavier Saegert
Mario Sarbia
Regine Schneider-Stock
Michael Vieth
Ellen C Zwarthoff
Arndt Hartmann
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEComprehensive Cancer Center Erlangen · DEBayreuth Medical Center · DEErasmus MC · NLErasmus University Rotterdam · NLKU Leuven · BEMedical University of Graz · ATPathologie Hamburg-West · DERadboud University Nijmegen · NLUniversitätsmedizin Göttingen · DEUniversity of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Criteria for the diagnosis of serrated colorectal lesions (hyperplastic polyp, sessile serrated adenoma without or with dysplasia--which we called mixed polyp--and traditional serrated adenoma) for which consensus has been reached should be validated for applicability in daily practice in terms of inter-observer reproducibility and their association with clinical features and (epi)genetic events. A study set was created from a consecutive series of colorectal polyps (n = 1,926) by selecting all sessile serrated adenomas, traditional serrated adenomas and mixed polyps. We added consecutive series of hyperplastic polyps, classical adenomas and normal mucosa samples for a total of 200 specimens. With this series, we conducted an inter-observer study, encompassing ten pathologists with gastrointestinal pathology experience from five European countries, in three rounds in which all cases were microscopically evaluated. An assessment of single morphological criteria was included, and these were correlated with clinical parameters and the mutation status of KRAS, BRAF and PIK3CA and the methylation status of MLH1. Gender, age and localisation were significantly associated with certain types of lesions. Kappa statistics revealed moderate to good inter-observer agreement for polyp classification (κ = 0.56 to 0.63), but for single criteria, this varied considerably (κ = 0.06 to 0.82). BRAF mutations were frequently found in hyperplastic polyps (86 %, 62/72) and sessile serrated adenomas (80 %, 41/51). KRAS mutations occurred more frequently in traditional serrated adenomas (78 %, 7/9) and less so in classical adenomas (20 %, 10/51). Single morphological criteria for sessile serrated adenomas showed significant correlation with BRAF mutation (all p ≤ 0.001), and those for classical adenomas or traditional serrated adenoma correlated significantly with KRAS mutation (all p < 0.001). Therefore, single well-defined morphological criteria are predictive for genetic alterations in colorectal polyps.

Indexed as

Adaptor Proteins, Signal TransducingAdenomatous PolypsClass I Phosphatidylinositol 3-KinasesColonic PolypsColorectal NeoplasmsFemaleHumansMaleMedical OncologyMutL Protein Homolog 1Nuclear ProteinsObserver VariationPhosphatidylinositol 3-KinasesPolymerase Chain ReactionProto-Oncogene ProteinsProto-Oncogene Proteins B-rafAdaptor Proteins, Signal TransducingBRAF protein, humanClass I Phosphatidylinositol 3-KinasesKRAS protein, humanMLH1 protein, humanMutL Protein Homolog 1Nuclear ProteinsPhosphatidylinositol 3-KinasesPIK3CA protein, humanProto-Oncogene ProteinsProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)ras Proteins

Identifiers

PMID24728704
OpenAlexW2097752450

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.