Evidence map›Paper›PMID 39887612›Full record

ArticleMolecular oncology2025

Peripheral blood leukocyte signatures as biomarkers in relapsed ovarian cancer patients receiving combined anti-CD73/anti-PD-L1 immunotherapy in arm A of the NSGO-OV-UMB1/ENGOT-OV30 trial.

Luka Tandaric, Annika Auranen, Katrin Kleinmanns, René DePont Christensen, Liv Cecilie Vestrheim Thomsen, Cara Ellen Wogsland, Emmet McCormack, Johanna Mäenpää, Kristine Madsen, Karen Stampe Petersson and 2 more

Abstract read
In one paragraph

Article in Molecular oncology, 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. Article
  2. Review
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

12 authors.

Luka TandaricCentre for Cancer Biomarkers CCBIO, Department of Clinical Science, University of Bergen, Norway.ORCID https://orcid.org/0009-0009-1431-2586
Annika AuranenDepartment of Obstetrics and Gynecology and Tays Cancer Centre, Tampere University Hospital, Finland.
Katrin KleinmannsCentre for Cancer Biomarkers CCBIO, Department of Clinical Science, University of Bergen, Norway.
René DePont ChristensenNordic Society of Gynaecological Oncology - Clinical Trial Unit (NSGO-CTU), Copenhagen, Denmark.
Liv Cecilie Vestrheim ThomsenCentre for Cancer Biomarkers CCBIO, Department of Clinical Science, University of Bergen, Norway.
Cara Ellen WogslandCentre for Cancer Biomarkers CCBIO, Department of Clinical Science, University of Bergen, Norway.
Emmet McCormackCentre for Cancer Biomarkers CCBIO, Department of Clinical Science, University of Bergen, Norway.
Johanna MäenpääDepartment of Obstetrics and Gynecology and Tays Cancer Centre, Tampere University Hospital, Finland.
Kristine MadsenNordic Society of Gynaecological Oncology - Clinical Trial Unit (NSGO-CTU), Copenhagen, Denmark.
Karen Stampe PeterssonNordic Society of Gynaecological Oncology - Clinical Trial Unit (NSGO-CTU), Copenhagen, Denmark.
Mansoor Raza MirzaNordic Society of Gynaecological Oncology - Clinical Trial Unit (NSGO-CTU), Copenhagen, Denmark.
Line BjørgeCentre for Cancer Biomarkers CCBIO, Department of Clinical Science, University of Bergen, Norway.

Funding

AstraZeneca United StatesHelse Vest 28543Norges Forskningsråd 223250
6 · The paper itself

Abstract

Immune checkpoint inhibitors have demonstrated limited efficacy in overcoming immunosuppression in patients with epithelial ovarian cancer (EOC). Although certain patients experience long-term treatment benefit, reliable biomarkers for responder pre-selection and the distinction of dominant immunosuppressive mechanisms have yet to be identified. Here, we used a 40-marker suspension mass cytometry panel to comprehensively phenotype peripheral blood leukocytes sampled over time from patients with relapsed EOC who underwent combination oleclumab (anti-CD73) and durvalumab (anti-PD-L1) immunotherapy in the NSGO-OV-UMB1/ENGOT-OV30 trial. We found that survival duration was impacted by baseline abundances of total peripheral blood mononuclear cells. Longitudinal analyses revealed a significant increase in CD14

Indexed as

B7-H1 AntigenBiomarkers, TumorCarcinoma, Ovarian EpithelialImmunotherapyLeukocytesNeoplasm Recurrence, LocalOvarian NeoplasmsAgedAntibodies, MonoclonalFemaleHumansMiddle AgedAntibodies, MonoclonalB7-H1 AntigenBiomarkers, TumorCD274 protein, humandurvalumabbiomarkersdurvalumabimmunotherapyliquid biopsyoleclumabovarian cancer

Identifiers

PMID39887612
PMCPMC12077279

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.