Evidence map›Paper›PMID 29558947›Full record

ArticleDiagnostic pathology2018

Does heterogeneity matter in the estimation of tumour budding and tumour stroma ratio in colon cancer?

Ann C Eriksen, Johnnie B Andersen, Jan Lindebjerg, René dePont Christensen, Torben F Hansen, Sanne Kjær-Frifeldt, Flemming B Sørensen

Abstract read
In one paragraph

Article in Diagnostic pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

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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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Tumor proportion in colon cancer: results from a semiautomatic image analysis approach.Virchows Archiv : an international journal of pathology · 2020
    Article
  9. Article
  10. 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

7 authors.

Ann C EriksenInstitute of Regional Health Research, University of Southern Denmark, Odense, Denmark. ann.christina.eriksen@rsyd.dk.
Johnnie B AndersenDepartment of Clinical Medicine, Stereological Research Laboratory and University Institute of Pathology, Aarhus University, Nørrebrogade 44, 10G, DK-8000, Aarhus C, Denmark.
Jan LindebjergInstitute of Regional Health Research, University of Southern Denmark, Odense, Denmark.
René dePont ChristensenResearch Unit of General Practice, University of Southern Denmark, J.B. Winsløws Vej 9 A, 1st, DK-5000, Odense C, Denmark.
Torben F HansenInstitute of Regional Health Research, University of Southern Denmark, Odense, Denmark.
Sanne Kjær-FrifeldtDepartment of Pathology, Danish Colorectal Cancer Center South, Vejle Hospital, Beriderbakken 4, DK-7100, Vejle, Denmark.
Flemming B SørensenInstitute of Regional Health Research, University of Southern Denmark, Odense, Denmark.

Funding

Dansk Kræftforsknings Fond 127.000 DKKThe Beckett Foundation 40.000 DKKThe Research Council of Lillebaelt Hospital 100.000 DKK
6 · The paper itself

Abstract

backgroundTumour budding (TB) and Tumour Stroma Ratio (TSR) may be rewarding in the treatment stratification of patients with stage II colon cancer. However, lack of standardization may exclude these parameters from being used in a clinical setting. The purpose of this methodologic study was to compare stereology with semi-quantitative estimations of TSR, to investigate the intra-tumoural heterogeneity of TB and TSR, and to assess the intra- and inter-observer agreement.

methodsThree paraffin embedded tumour blocks, one of them representing the deepest invasive front, were selected from each of 43 patients treated for stage II colon cancer. TSR was estimated in H&E sections semi-quantitatively using conventional microscopy, and stereologically on scanned slides, using the newCAST stereology platform. TB was scored across 10 high power fields at the invasive front in cytokeratin AE1/AE3 stained sections.

resultsSubjective, semi-quantitative estimates of TSR significantly correlated to the stereological estimates, with the best correlation found for sections with the deepest invasive tumour penetration (σ = 0.621, p < 0.001). Inter-observer agreement was moderate to substantial for both TB (Κappa = 0.46-0.73) and TSR (Κappa = 0.70-0.75). The Intraclass correlation coefficient (ICC) for TSR varied from 0.322 based on stereological hotspot estimation to 0.648 for the semi-quantitative evaluation. For TB, ICC varied from 0.646 based on continuous data to 0.698 based on categorical data (cut-off: 10 buds). Thus, the intra-tumoural heterogeneity for both TB and the semi-quantitative estimation of TSR was low.

conclusionWe recommend using only one tissue section representing the deepest invasive tumour area for estimation of TSR. For TB we recommend using one tissue section; however due to low representation of high-budding tumours, results must be considered with caution.

Indexed as

AdenocarcinomaAdultAgedColonic NeoplasmsColorectal NeoplasmsFemaleHumansImmunohistochemistryMaleMiddle AgedPrognosisSoft Tissue NeoplasmsColon cancerHeterogeneityTumour buddingTumour stroma ratio

Identifiers

PMID29558947
PMCPMC5859415

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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.