Evidence map›Paper›PMID 34174109›Full record

ArticleHistopathology2021

Stromal composition predicts recurrence of early rectal cancer after local excision.

Helen J S Jones, Chris Cunningham, Hanne A Askautrud, Håvard E Danielsen, David J Kerr, Enric Domingo, Tim Maughan, Simon J Leedham, Viktor H Koelzer

Open access · hybridAbstract read
In one paragraph

Article in Histopathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 19% 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, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Helen J S JonesDepartment of Colorectal Surgery, Oxford University Hospitals NHS Trust, Oxford, UK.ORCID https://orcid.org/0000-0001-8238-7779
Chris CunninghamDepartment of Colorectal Surgery, Oxford University Hospitals NHS Trust, Oxford, UK.
Hanne A AskautrudInstitute for Cancer Genetics and Informatics, Oslo University Hospital, Oslo, Norway.
Håvard E DanielsenInstitute for Cancer Genetics and Informatics, Oslo University Hospital, Oslo, Norway.
David J KerrNuffield Division of Clinical Laboratory Sciences, University of Oxford, Oxford, UK.
Enric DomingoDepartment of Oncology, MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, UK.
Tim MaughanDepartment of Oncology, MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, UK.
Simon J LeedhamIntestinal Stem Cell Biology Laboratory, Nuffield Department of Medicine, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Viktor H KoelzerDepartment of Pathology and Molecular Pathology, University and University Hospital Zürich, Zürich, Switzerland.ORCID https://orcid.org/0000-0001-9206-4885
University of Oxford · GBOslo University Hospital · NOOxford University Hospitals NHS Trust · GBCentre for Human Genetics · GB

Funding

Bowel Disease Research FoundationMedical Research Council MR/M016587/1NIHR Biomedical Research CentreOxford Colon Cancer Trust (Occtopus)Promedica Foundation F-87701-41-01Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung P2SKP3_168322/1Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung P2SKP3_168322/2Wellcome TrustWellcome Trust 090532/Z/09/ZWellcome Trust 203141/Z/16/ZWellcome Trust 206314/Z/17/ZWerner-Hedy Berger Janser Foundation
6 · The paper itself

Abstract

aimsAfter local excision of early rectal cancer, definitive lymph node status is not available. An alternative means for accurate assessment of recurrence risk is required to determine the most appropriate subsequent management. Currently used measures are suboptimal. We assess three measures of tumour stromal content to determine their predictive value after local excision in a well-characterised cohort of rectal cancer patients without prior radiotherapy. METHODS AND

resultsA total of 143 patients were included. Haematoxylin and eosin (H&E) sections were scanned for (i) deep neural network (DNN, a machine-learning algorithm) tumour segmentation into compartments including desmoplastic stroma and inflamed stroma; and (ii) digital assessment of tumour stromal fraction (TSR) and optical DNA ploidy analysis. 3' mRNA sequencing was performed to obtain gene expression data from which stromal and immune scores were calculated using the ESTIMATE method. Full results were available for 139 samples and compared with disease-free survival. All three methods were prognostic. Most strongly predictive was a DNN-determined ratio of desmoplastic to inflamed stroma >5.41 (P < 0.0001). A ratio of ESTIMATE stromal to immune score <1.19 was also predictive of disease-free survival (P = 0.00051), as was stromal fraction >36.5% (P = 0.037).

conclusionsThe DNN-determined ratio of desmoplastic to inflamed ratio is a novel and powerful predictor of disease recurrence in locally excised early rectal cancer. It can be assessed on a single H&E section, so could be applied in routine clinical practice to improve the prognostic information available to patients and clinicians to inform the decision concerning further management.

Indexed as

Tumor MicroenvironmentAgedCohort StudiesFemaleHumansImage Interpretation, Computer-AssistedMaleMiddle AgedNeoplasm Recurrence, LocalNeural Networks, ComputerRectal NeoplasmsRetrospective StudiesStromal Cellsdesmoplastic stromaearly rectal cancerinflamed stroma local excisionprognostic factorstroma

Identifiers

PMID34174109
PMCPMC8845517
OpenAlexW3177290741

What OpenQuestion holds

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Registered trials

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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.