Evidence map›Paper›PMID 32503947›Full record

ArticleJournal for immunotherapy of cancer2020

Circulating CD14

Mélissa Prat, Augustin Le Naour, Kimberley Coulson, Fanny Lemée, Hélène Leray, Godefroy Jacquemin, Mouna Chirine Rahabi, Léa Lemaitre, Hélène Authier, Gwenaël Ferron and 9 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02978755 (Open, Non Controlled, Multicenter, First-in-Human Study for the Evaluation of the Safety, Pharmacokinetics and Preliminary Antitumor Activity of GM102 in Patients With Advanced Pretreated Gynecological Cancer), which is not on this map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 19% 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.

NCT02978755 phase1completednot on this map

Open, Non Controlled, Multicenter, First-in-Human Study for the Evaluation of the Safety, Pharmacokinetics and Preliminary Antitumor Activity of GM102 in Patients With Advanced Pretreated Gynecological Cancer

TypeinterventionalSponsorGamaMabs PharmaRan2016 to 2020Enrolled78ConditionsNeoplasm, GynecologicArmsGM102, GM102 escalating doses
3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Heterogeneity of monocytes in cancer.American journal of cancer research · 2025
    Review
  18. Review
  19. Article
  20. 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

19 authors at 2 institutions in 1 country.

Mélissa Prat *UMR152 Pharmadev, Université Toulouse III Paul Sabatier, Toulouse, Occitanie, France.
Augustin Le Naour *UMR152 Pharmadev, Université Toulouse III Paul Sabatier, Toulouse, Occitanie, France.
Kimberley CoulsonUMR152 Pharmadev, Université Toulouse III Paul Sabatier, Toulouse, Occitanie, France.
Fanny LeméeGamamabs Pharma, Toulouse, Languedoc-Roussillon-Midi, France.
Hélène LerayUMR1037, CRCT, Toulouse, Midi-Pyrénées, France.
Godefroy JacqueminUMR152 Pharmadev, Université Toulouse III Paul Sabatier, Toulouse, Occitanie, France.
Mouna Chirine RahabiUMR152 Pharmadev, Université Toulouse III Paul Sabatier, Toulouse, Occitanie, France.
Léa LemaitreUMR1037, CRCT, Toulouse, Midi-Pyrénées, France.
Hélène AuthierUMR152 Pharmadev, Université Toulouse III Paul Sabatier, Toulouse, Occitanie, France.
Gwenaël FerronInstitut Claudius Regaud, IUCT Oncopole, Toulouse, Languedoc-Roussillon-Midi, France.
Jean-Marc BarretGamamabs Pharma, Toulouse, Languedoc-Roussillon-Midi, France.
Alejandra MartinezInstitut Claudius Regaud, IUCT Oncopole, Toulouse, Languedoc-Roussillon-Midi, France.
Maha AyyoubUMR1037, CRCT, Toulouse, Midi-Pyrénées, France.
Jean-Pierre DelordInstitut Claudius Regaud, IUCT Oncopole, Toulouse, Languedoc-Roussillon-Midi, France.
Laurence GladieffInstitut Claudius Regaud, IUCT Oncopole, Toulouse, Languedoc-Roussillon-Midi, France.
Isabelle Tabah-FischGamamabs Pharma, Toulouse, Languedoc-Roussillon-Midi, France.
Jean-François ProstGamamabs Pharma, Toulouse, Languedoc-Roussillon-Midi, France.
Bettina CoudercUMR1037, CRCT, Toulouse, Midi-Pyrénées, France.
Agnès CosteUMR152 Pharmadev, Université Toulouse III Paul Sabatier, Toulouse, Occitanie, France agnes.coste@univ-tlse3.fr.ORCID 0000-0001-7781-3323
Institut Claudius Regaud · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBesides the interest of an early detection of ovarian cancer, there is an urgent need for new predictive and prognostic biomarkers of tumor development and cancer treatment. In healthy patients, circulating blood monocytes are typically subdivided into classical (85%), intermediate (5%) and non-classical (10%) populations. Although these circulating monocyte subsets have been suggested as biomarkers in several diseases, few studies have investigate their potential as a predictive signature for tumor immune status,tumor growth and treatment adaptation.

methodsIn this study, we used a homogeneous cohort of 28 chemotherapy-naïve patients with ovarian cancer to evaluate monocyte subsets as biomarkers of the ascites immunological status. We evaluated the correlations between circulating monocyte subsets and immune cells and tumor burden in peritoneal ascites. Moreover, to validate the use of circulating monocyte subsets tofollow tumor progression and treatment response, we characterized blood monocytes from ovarian cancer patients included in a phase 1 clinical trial at baseline and following murlentamab treatment.

resultsWe demonstrate here a robust expansion of the intermediate blood monocytes (IBMs) in ovarian cancer patients. We establish a significant positive correlation between IBM percentage and tumor-associate macrophages with a CCR2

conclusionsThis study, which links IBM level with immunosuppression and tumor burden in peritoneum, identifies IBMs as apotential predictive signature of ascites immune status and as a biomarker ofovarian cancer development and treatment response. TRIAL REGISTRATION NUMBER: EudraCT: 2015-004252-22 NCT02978755.

Indexed as

AscitesBiomarkers, TumorDisease ProgressionFemaleHumansImmunotherapyLipopolysaccharide ReceptorsMonocytesReceptors, IgGTumor MicroenvironmentBiomarkers, TumorLipopolysaccharide ReceptorsReceptors, IgGbiomarkers, tumorimmunityimmunotherapymacrophagestumor microenvironment

Identifiers

PMID32503947
PMCPMC7279676
OpenAlexW3033530735

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.