Evidence map›Paper›PMID 38407700›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2024

The prognostic effect of tumor-associated macrophages in stage I-III colorectal cancer depends on T cell infiltration.

Umair Majid, Christian Holst Bergsland, Anita Sveen, Jarle Bruun, Ina Andrassy Eilertsen, Espen S Bækkevold, Arild Nesbakken, Sheraz Yaqub, Frode L Jahnsen, Ragnhild A Lothe

Open access · hybridAbstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Umair Majid *Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Christian Holst Bergsland *Department of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Anita SveenDepartment of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Jarle BruunDepartment of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Ina Andrassy EilertsenDepartment of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Espen S BækkevoldDepartment of Pathology, Oslo University Hospital-Rikshospitalet, Oslo, Norway.
Arild NesbakkenDepartment of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Sheraz YaqubInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Frode L JahnsenInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Ragnhild A LotheDepartment of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway. r.a.lothe@medisin.uio.no.
University of Oslo · NOOslo University Hospital · NO

Funding

Helse Sør-Øst RHF 2021058Kreftforeningen 208336-2019
6 · The paper itself

Abstract

backgroundTumor-associated macrophages (TAMs) are associated with unfavorable patient prognosis in many cancer types. However, TAMs are a heterogeneous cell population and subsets have been shown to activate tumor-infiltrating T cells and confer a good patient prognosis. Data on the prognostic value of TAMs in colorectal cancer are conflicting. We investigated the prognostic effect of TAMs in relation to tumor-infiltrating T cells in colorectal cancers.

methodsThe TAM markers CD68 and CD163 were analyzed by multiplex fluorescence immunohistochemistry and digital image analysis on tissue microarrays of 1720 primary colorectal cancers. TAM density in the tumor stroma was scored in relation to T cell density (stromal CD3

resultsHigh TAM density was associated with a favorable 5-year relapse-free survival in a multivariable model of patients with stage I-III tumors (p = 0.004, hazard ratio 0.94, 95% confidence interval 0.90-0.98). However, the prognostic effect was dependent on tumoral T-cell density. High TAM density was associated with a good prognosis in patients who also had high T-cell levels in their tumors, while high TAM density was associated with poorer prognosis in patients with low T-cell levels (p

conclusionsThis study supported a phenotypic heterogeneity of TAMs in colorectal cancer, and showed that combined tumor immunophenotyping of multiple immune cell types improved the prediction of patient prognosis.

Indexed as

Colorectal NeoplasmsLymphocytes, Tumor-InfiltratingNeoplasm StagingTumor-Associated MacrophagesAdultAgedAged, 80 and overAntigens, CDAntigens, Differentiation, MyelomonocyticFemaleHumansMaleMiddle AgedPrognosisProportional Hazards ModelsT-LymphocytesAntigens, CDAntigens, Differentiation, MyelomonocyticColorectal cancerImmune tumor microenvironmentMultiplex fluorescence immunohistochemistryPrognostic markersT cellsTumor associated macrophages

Identifiers

PMID38407700
PMCPMC11322253
OpenAlexW4392157375

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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.