Evidence map›Paper›PMID 40594059›Full record

ArticleScientific reports2025

Clinical and immunopathological evaluation and its comparison with IHC consensus molecular subtypes of colorectal cancer.

Eduardo Feliciangeli, Ana Albaladejo-González, José García-Rodríguez, Antonio Lázaro-Sánchez, Rosanna Borg, Paola Pimentel-Cáceres, Diego Soriano-Polo, Edith Rodríguez-Braun, José Balsalobre-Yago, María José Martínez-Ortiz and 6 more

Abstract readComparative Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Review
  2. 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

16 authors.

Eduardo FeliciangeliMedical Oncology Department, Hospital General Universitario Santa Lucía, Cartagena, Spain. edufeliciangeli@gmail.com.
Ana Albaladejo-GonzálezHealth Sciences Faculty, Universidad Católica de Murcia (UCAM), Guadalupe, Spain.
José García-RodríguezLaboratory Medicine and Pathology Department, Hospital General Universitario Santa Lucía, Cartagena, Spain.
Antonio Lázaro-SánchezGroup of Molecular Pathology and Pharmacogenetics, Instituto Murciano de Investigación Biosanitaria (IMIB), Hospital Universitario Santa Lucía, Cartagena, Spain.
Rosanna BorgVan Hall Larenstein University of Applied Sciences, Agora 1, P.O. Box 1528, 8901 BV, Leeuwarden, The Netherlands.
Paola Pimentel-CáceresMedical Oncology Department, Hospital General Universitario Santa Lucía, Cartagena, Spain.
Diego Soriano-PoloMedical Oncology Department, Hospital General Universitario Santa Lucía, Cartagena, Spain.
Edith Rodríguez-BraunMedical Oncology Department, Hospital General Universitario Santa Lucía, Cartagena, Spain.
José Balsalobre-YagoMedical Oncology Department, Hospital General Universitario Santa Lucía, Cartagena, Spain.
María José Martínez-OrtizMedical Oncology Department, Hospital General Universitario Santa Lucía, Cartagena, Spain.
Sofía Wikström-FernándezMedical Oncology Department, Hospital General Universitario Santa Lucía, Cartagena, Spain.
Andrés Murillo-HerreraMedical Oncology Department, Hospital General Universitario Santa Lucía, Cartagena, Spain.
Teresa García-GarcíaMedical Oncology Department, Hospital General Universitario Santa Lucía, Cartagena, Spain.
José García-SolanoGroup of Molecular Pathology and Pharmacogenetics, Instituto Murciano de Investigación Biosanitaria (IMIB), Hospital Universitario Santa Lucía, Cartagena, Spain.
Pablo Conesa-ZamoraGroup of Molecular Pathology and Pharmacogenetics, Instituto Murciano de Investigación Biosanitaria (IMIB), Hospital Universitario Santa Lucía, Cartagena, Spain. pconesa@ucam.edu.
Ginés Luengo-GilGroup of Molecular Pathology and Pharmacogenetics, Instituto Murciano de Investigación Biosanitaria (IMIB), Hospital Universitario Santa Lucía, Cartagena, Spain. gluengo@ucam.edu.

Funding

European Commission GA: 848098Instituto de Salud Carlos III ICI20/00044Sociedad Española de Oncología Médica Beca SEOM/MSD para Proyectos de Investigación
6 · The paper itself

Abstract

This study examined the prognostic significance of immunoscore within consensus molecular subtypes (CMS), tumour budding (TB), and macrophage infiltration in colorectal cancer (CRC). A retrospective series was analysed using immunohistochemical staining, immunoscore evaluation, and CMS classification, according to established methods. Among the 255 patients with CRC, 34.9% had stage III disease. The CMS classification showed a predominance of CMS2/3 (69.4%), with relapse occurring across all the subtypes. Low immunoscore was frequent in conventional and serrated adenocarcinomas, as well as in CMS2/3, whereas MSI-H correlated with intermediate-high immunoscore. TB was prevalent in relapsed patients, particularly in CMS2/3 and CMS4, and was linked to serrated histology. TB of ≥ 20 foci was correlated with hepatic metastases. CD163+ macrophage infiltration was common in CMS1 and CMS2/3, and was associated with high immune scores. TB influenced overall and relapse-free survival, whereas CMS affected the overall survival. Immunoscore were not associated with survival. The associations identified between CMS subtypes and clinical as well as pathological characteristics enhance the understanding of CMS behaviour in clinical practice.

Indexed as

Colorectal NeoplasmsAdultAgedAged, 80 and overAntigens, CDBiomarkers, TumorCD163 AntigenFemaleHumansImmunohistochemistryMacrophagesMaleMiddle AgedNeoplasm Recurrence, LocalNeoplasm StagingPrognosisAntigens, CDBiomarkers, TumorCD163 Antigen

Identifiers

PMID40594059
PMCPMC12215256

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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.