Evidence map›Paper›PMID 33837301›Full record

ArticleBritish journal of cancer2021

The circulating soluble form of the CD40 costimulatory immune checkpoint receptor and liver metastasis risk in rectal cancer.

Sebastian Meltzer, Annette Torgunrud, Hanna Abrahamsson, Arne Mide Solbakken, Kjersti Flatmark, Svein Dueland, Kine Mari Bakke, Paula Anna Bousquet, Anne Negård, Christin Johansen and 5 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05504252 (METIMMOX-2), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 18% 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.

NCT05504252 phase2active not recruitingnot on this mapstarted 2022, after this paper: background citation

METIMMOX-2: Metastatic pMMR/MSS Colorectal Cancer - Shaping Anti-Tumor Immunity by Oxaliplatin

TypeinterventionalSponsorUniversity Hospital, AkershusRan2022 to 2028Enrolled80ConditionsColorectal Adenocarcinoma, Mucinous Adenocarcinoma, Signet Ring Cell AdenocarcinomaArmsNivolumab, Oxaliplatin
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 16 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

15 authors at 5 institutions in 2 countries.

Sebastian MeltzerDepartment of Oncology, Akershus University Hospital, Lørenskog, Norway. sebastian.meltzer@medisin.uio.no.ORCID http://orcid.org/0000-0001-6640-3927
Annette Torgunrud *Department of Tumour Biology, Oslo University Hospital, Oslo, Norway.
Hanna Abrahamsson *Department of Oncology, Akershus University Hospital, Lørenskog, Norway.
Arne Mide SolbakkenDepartment of Gastroenterological Surgery, Oslo University Hospital, Oslo, Norway.
Kjersti FlatmarkDepartment of Tumour Biology, Oslo University Hospital, Oslo, Norway.
Svein DuelandDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
Kine Mari BakkeDepartment of Oncology, Akershus University Hospital, Lørenskog, Norway.
Paula Anna BousquetDepartment of Oncology, Akershus University Hospital, Lørenskog, Norway.
Anne NegårdInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Christin JohansenDepartment of Oncology, Akershus University Hospital, Lørenskog, Norway.
Lars Gustav LyckanderDepartment of Pathology, Akershus University Hospital, Lørenskog, Norway.
Finn Ole LarsenDepartment of Oncology, Herlev and Gentofte Hospital, Herlev, Denmark.
Jakob Vasehus SchouDepartment of Oncology, Herlev and Gentofte Hospital, Herlev, Denmark.
Kathrine Røe RedalenDepartment of Physics, Norwegian University of Science and Technology, Trondheim, Norway.
Anne Hansen ReeDepartment of Oncology, Akershus University Hospital, Lørenskog, Norway.ORCID http://orcid.org/0000-0002-8264-3223
Akershus University Hospital · NOOslo University Hospital · NOUniversity of Oslo · NOGentofte Hospital · DKNorwegian University of Science and Technology · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn colorectal cancer, the inflamed tumour microenvironment with its angiogenic activities is immune- tolerant and incites progression to liver metastasis. We hypothesised that angiogenic and inflammatory factors in serum samples from patients with non-metastatic rectal cancer could inform on liver metastasis risk.

methodsWe measured 84 angiogenic and inflammatory markers in serum sampled at the time of diagnosis within the population-based cohort of 122 stage I-III patients. In a stepwise manner, the statistically strongest proteins associated with time to development of liver metastasis were analysed in the corresponding serum samples from 273 stage II-III rectal cancer patients in three independent cohorts.

resultsWe identified the soluble form of the costimulatory immune checkpoint receptor cluster of differentiation molecule 40 (sCD40) as a marker of liver metastasis risk across all patient cohorts-the higher the sCD40 level, the shorter time to liver metastasis. In patients receiving neoadjuvant treatment, the sCD40 value remained an independent variable associated with progression to liver metastasis along with the local treatment response. Of note, serum sCD40 was not associated with progression to lung metastasis.

conclusionsCirculating sCD40 is a marker of liver metastasis risk in rectal cancer and may be developed for use in clinical practice.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCD40 AntigensDisease ProgressionFemaleHumansLiver NeoplasmsMaleMiddle AgedNeoplasm StagingProspective StudiesRectal NeoplasmsTumor MicroenvironmentBiomarkers, TumorCD40 Antigens

Identifiers

PMID33837301
PMCPMC8292313
OpenAlexW3143341125

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Registered trials

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.