Evidence map›Paper›PMID 41984263›Full record

ArticleJournal of gastrointestinal cancer2026

Survival and Tumour Microenvironment in Spatially Distinct Regions in Patients Resected for Hepatocellular Carcinoma: A Multicentre Study.

Sophie Bull Nordkild, Jeanett Klubien, Delal Akdag, Colm O'Rourke, Jeanette Baehr Georgsen, Patricia Switten Nielsen, Torben Steiniche, Gerda Elisabeth Villadsen, Anders Riegels Knudsen, Gro Linno Willemoe and 3 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of gastrointestinal cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Sophie Bull NordkildDepartment of Digestive Diseases, Transplantation and General Surgery, Rigshospitalet, Inge Lehmanns Vej 7, Copenhagen Ø, 2100, Denmark.
Jeanett KlubienDepartment of Digestive Diseases, Transplantation and General Surgery, Rigshospitalet, Inge Lehmanns Vej 7, Copenhagen Ø, 2100, Denmark.
Delal AkdagDepartment of Digestive Diseases, Transplantation and General Surgery, Rigshospitalet, Inge Lehmanns Vej 7, Copenhagen Ø, 2100, Denmark.
Colm O'RourkeBiotech Research and Innovation Centre (BRIC), Department of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Jeanette Baehr GeorgsenDepartment of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Patricia Switten NielsenDepartment of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Torben SteinicheDepartment of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Gerda Elisabeth VilladsenDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Anders Riegels KnudsenDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Gro Linno WillemoeDepartment of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Jesper Bøje AndersenBiotech Research and Innovation Centre (BRIC), Department of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Susanne Dam NielsenDepartment of Digestive Diseases, Transplantation and General Surgery, Rigshospitalet, Inge Lehmanns Vej 7, Copenhagen Ø, 2100, Denmark.
Hans-Christian Lykkegaard PommergaardDepartment of Digestive Diseases, Transplantation and General Surgery, Rigshospitalet, Inge Lehmanns Vej 7, Copenhagen Ø, 2100, Denmark. hans-christian.pommergaard@regionh.dk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe tumour microenvironment (TME) may play a pivotal role in the development, progression, and prognosis of HCC. We aimed to investigate the prognostic association of the TME in Danish liver-resected patients with HCC.

methodsWe included all patients liver-resected for HCC between January 2000 and December 2016 with available tumour tissue stored in the diagnostic biobank. Resected tumour tissues and corresponding normal liver tissues were investigated for immune cell densities with immunohistochemistry. We investigated the association between individual immune cell densities and prognosis. We identified distinct patient groups based on hierarchical clustering and heatmap visualisation, for their association with prognosis.

resultsWe included 75 patients, 72% were male and median age was 66 years (58-72). Most patients had a single tumour, median size was 50 mm, and 57% without vascular invasion. Median follow-up was 44 months and 50% of the patients had a recurrence within the study period. The density of CD4+ T cells in the invasive margin was significantly associated with a higher risk of mortality (HR = 1.43, 95% CI: 1.13–1.82), whereas a higher density of tumour-associated macrophages in the tumour centre was significantly associated with a lower risk of cancer-related mortality (HR = 0.53, 95% CI: 0.28–1.00). Clustering of patients based on immune cell densities in tumour tissue revealed that those with lower immune cell counts exhibited significantly worse disease-free survival when compared to other patients (p= 0.03).

conclusionThe TME had a prognostic association with survival, lending credence to spatial immune cell densities as important factors contributing to prognosis.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsNeoplasm Recurrence, LocalTumor MicroenvironmentAgedCD4-Positive T-LymphocytesDenmarkFemaleFollow-Up StudiesHepatectomyHumansLiverMaleMiddle AgedPrognosisTumor-Associated MacrophagesHepatocellular carcinomaImmune cellsImmunohistochemistryLiver resectionPrognosisTumour microenvironment

Identifiers

PMID41984263
PMCPMC13083490

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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.