Evidence map›Paper›PMID 39511626›Full record

ArticleJournal of experimental & clinical cancer research : CR2024

Soluble and EV-bound CD27 act as antagonistic biomarkers in patients with solid tumors undergoing immunotherapy.

Joao Gorgulho, Sven H Loosen, Ramsha Masood, Franziska Giehren, Francesca Pagani, Gustav Buescher, Lorenz Kocheise, Vincent Joerg, Constantin Schmidt, Kornelius Schulze and 23 more

Abstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 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
–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

10 citing papers in PubMed.

  1. Review
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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

33 authors.

Joao Gorgulho *Department of Oncology, Hematology and Bone Marrow Transplantation With Section of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Sven H Loosen *Department of Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Ramsha MasoodI. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Franziska GiehrenI. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Francesca PaganiI. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Gustav BuescherI. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Lorenz KocheiseI. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Vincent JoergI. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Constantin SchmidtI. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Kornelius SchulzeI. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Christoph RoderburgDepartment of Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Eva KinkelUniversity Cancer Center Hamburg - Hubertus Wald Tumorzentrum, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Britta FritzscheUniversity Cancer Center Hamburg - Hubertus Wald Tumorzentrum, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Simon WehmeyerDepartment of Oncology, Hematology and Bone Marrow Transplantation With Section of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Benjamin SchmidtDepartment of Oncology, Hematology and Bone Marrow Transplantation With Section of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Paul KachelDepartment of Oncology, Hematology and Bone Marrow Transplantation With Section of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Christina RollingDepartment of Oncology, Hematology and Bone Marrow Transplantation With Section of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Julian GötzeDepartment of Oncology, Hematology and Bone Marrow Transplantation With Section of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Alina BuschDepartment of Oncology, Hematology and Bone Marrow Transplantation With Section of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Marianne SinnDepartment of Oncology, Hematology and Bone Marrow Transplantation With Section of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Thais Pereira-VeigaDepartment of Tumor Biology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Harriet WikmanDepartment of Tumor Biology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Maria GeffkenInstitute of Transfusion Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Sven PeineInstitute of Transfusion Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Urte MatschlLeibniz Institute of Virology, Hamburg, Germany.
Markus AltfeldLeibniz Institute of Virology, Hamburg, Germany.
Samuel HuberI. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Ansgar W LohseI. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Fabian BeierCenter for Integrated Oncology, Aachen-Bonn-Cologne-Düsseldorf (CIOABCD), Aachen, Germany.
Tim H BrümmendorfCenter for Integrated Oncology, Aachen-Bonn-Cologne-Düsseldorf (CIOABCD), Aachen, Germany.
Carsten BokemeyerDepartment of Oncology, Hematology and Bone Marrow Transplantation With Section of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Tom Luedde *Department of Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University Düsseldorf, Düsseldorf, Germany. luedde@hhu.de.
Johann von Felden *I. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany. j.von-felden@uke.de.

Funding

Bundesministerium für Bildung und Forschung 01EO2106Deutsche Forschungsgemeinschaft 279874820Deutsche Forschungsgemeinschaft 440603Deutsche Forschungsgemeinschaft 461704932Deutsche Krebshilfe 70114893European Research Council 771083
6 · The paper itself

Abstract

backgroundThe major breakthrough in cancer therapy with immune checkpoint inhibitors (ICIs) has highlighted the important role of immune checkpoints in antitumoral immunity. However, most patients do not achieve durable responses, making biomarker research in this setting essential. CD27 is a well known costimulatory molecule, however the impact of its soluble form in ICI is poorly investigated. Therefore, we aimed at testing circulating concentrations of soluble CD27 (sCD27) and CD27 bound to extracellular vesicles (EVs) as potential biomarkers to predict response and overall survival (OS) in patients undergoing ICI.

methodsSerum and plasma levels of sCD27 were assessed by immunoassay in three patient cohorts (n = 187) with advanced solid malignancies including longitudinal samples (n = 126): a training (n = 84, 210 specimens, Aachen ICI) and validation cohort (n = 70, 70 specimens, Hamburg ICI), both treated with ICI therapy, and a second independent validation cohort (n = 33, 33 specimens, Hamburg non-ICI) undergoing systemic therapy without any ICI. In a subset (n = 36, 36 baseline and 108 longitudinal specimens), EV-bound CD27 from serum was measured, while EV characterization studies were conducted on a fourth cohort (n = 45).

resultsIn the Aachen and Hamburg ICI cohorts, patients with lower circulating sCD27 levels before and during ICI therapy had a significantly longer progression-free survival (PFS) and OS compared to patients with higher levels, a finding that was confirmed by multivariate analysis (MVA) (Aachen ICI: p

conclusionSoluble and EV-bound CD27 appear to have opposing immunomodulatory functions and may represent easily measurable, non-invasive prognostic markers to predict response and survival in patients undergoing ICI therapy.

Indexed as

Biomarkers, TumorExtracellular VesiclesImmunotherapyNeoplasmsTumor Necrosis Factor Receptor Superfamily, Member 7AdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedBiomarkers, TumorTumor Necrosis Factor Receptor Superfamily, Member 7BiomarkerImmunotherapyLiquid biopsyPD-1PrognosisSoluble immune checkpoints

Identifiers

PMID39511626
PMCPMC11545160

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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.