Evidence map›Paper›PMID 38853386›Full record

ReviewThe journal of pathology. Clinical research2024

The Glasgow Microenvironment Score: an exemplar of contemporary biomarker evolution in colorectal cancer.

Katrina Knight, Christopher Bigley, Kathryn Pennel, Jennifer Hay, Noori Maka, Donald McMillan, James Park, Campbell Roxburgh, Joanne Edwards

Abstract readReview
In one paragraph

Review in The journal of pathology. Clinical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  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

9 authors.

Katrina KnightAcademic Unit of Surgery, Glasgow Royal Infirmary, School of Medicine, Dentistry and Nursing, University of Glasgow, Glasgow, UK.ORCID 0000-0002-0300-546X
Christopher BigleySchool of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0001-5820-9366
Kathryn PennelSchool of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0003-0186-1331
Jennifer HayGlasgow Tissue Research Facility, Queen Elizabeth University Hospital, Glasgow, UK.
Noori MakaDepartment of Pathology, Queen Elizabeth University Hospital, Glasgow, UK.
Donald McMillanAcademic Unit of Surgery, Glasgow Royal Infirmary, School of Medicine, Dentistry and Nursing, University of Glasgow, Glasgow, UK.ORCID 0000-0003-4260-5334
James ParkAcademic Unit of Surgery, Glasgow Royal Infirmary, School of Medicine, Dentistry and Nursing, University of Glasgow, Glasgow, UK.ORCID 0000-0002-6551-2037
Campbell RoxburghAcademic Unit of Surgery, Glasgow Royal Infirmary, School of Medicine, Dentistry and Nursing, University of Glasgow, Glasgow, UK.ORCID 0000-0002-2649-6695
Joanne EdwardsSchool of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0002-7192-6906

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer remains a leading cause of mortality worldwide. Significant variation in response to treatment and survival is evident among patients with similar stage disease. Molecular profiling has highlighted the heterogeneity of colorectal cancer but has had limited impact in daily clinical practice. Biomarkers with robust prognostic and therapeutic relevance are urgently required. Ideally, biomarkers would be derived from H&E sections used for routine pathological staging, have reliable sensitivity and specificity, and require minimal additional training. The biomarker targets would capture key pathological features with proven additive prognostic and clinical utility, such as the local inflammatory response and tumour microenvironment. The Glasgow Microenvironment Score (GMS), first described in 2014, combines assessment of peritumoural inflammation at the invasive margin with quantification of tumour stromal content. Using H&E sections, the Klintrup-Mäkinen (KM) grade is determined by qualitative morphological assessment of the peritumoural lymphocytic infiltrate at the invasive margin and tumour stroma percentage (TSP) calculated in a semi-quantitative manner as a percentage of stroma within the visible field. The resulting three prognostic categories have direct clinical relevance: GMS 0 denotes a tumour with a dense inflammatory infiltrate/high KM grade at the invasive margin and improved survival; GMS 1 represents weak inflammatory response and low TSP associated with intermediate survival; and GMS 2 tumours are typified by a weak inflammatory response, high TSP, and inferior survival. The prognostic capacity of the GMS has been widely validated while its potential to guide chemotherapy has been demonstrated in a large phase 3 trial cohort. Here, we detail its journey from conception through validation to clinical translation and outline the future for this promising and practical biomarker.

Indexed as

Biomarkers, TumorColorectal NeoplasmsTumor MicroenvironmentHumansNeoplasm GradingPrognosisBiomarkers, Tumorbiomarkerscolonic cancerhistopathologyinflammationmicroenvironment scoreprognosisrectal cancerstromal invasionsubtypestumour microenvironment

Identifiers

PMID38853386
PMCPMC11163018

What OpenQuestion holds

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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.