Evidence map›Paper›PMID 39903903›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2025

Combined Analyses of Circulating Tumor DNA and Immunoscore in Patients With Stage III Colon Cancer: A Post Hoc Analysis of the PRODIGE-GERCOR IDEA-France/HORG-IDEA-Greece Trials.

Julien Taieb, John Souglakos, Ioannis Boukovinas, Antoine Falcoz, Franck Pages, Ippokratis Messaritakis, Jaafar Bennouna, Pascal Artru, Christophe Louvet, Celine Lepere and 12 more

Abstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Significance of Th1 and Th2 Cell Densities and Th1/Th2 Cytokine Profiles in Colorectal Cancer.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2025
    Article
  11. 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

22 authors.

Julien TaiebDepartment of Gastroenterology and Gastrointestinal Oncology, CARPEM Comprehensive Cancer Center, Georges-Pompidou European Hospital, AP-HP, Paris, France.ORCID 0000-0002-9955-4753
John SouglakosDepartment of Medical Oncology, University Hospital of Heraklion, Crete, Greece.
Ioannis BoukovinasOncology Unit, Bioclinic, Thessaloniki, Greece.ORCID 0000-0003-4475-1802
Antoine FalcozMethodology and Quality of Life in Oncology Unit, Besançon University Hospital, Besançon, France.
Franck PagesDepartment of Immunology, Georges-Pompidou European Hospital, AP-HP, INSERM, Laboratory of Integrative Cancer Immunology, Equipe Labellisée Ligue Contre le Cancer, Centre de Recherche des Cordeliers, SIRIC CARPEM, Université Paris-Cité, Paris, France.ORCID 0000-0002-2083-610X
Ippokratis MessaritakisLaboratory of Translational Oncology, Medical School, University of Crete, Heraklion, Greece.ORCID 0000-0003-1877-500X
Jaafar BennounaDepartment of Medical Oncology, Hospital Foch, Suresnes, France.
Pascal ArtruDepartment of Medical Oncology, Private Hospital Jean Mermoz-Ramsay Santé, Lyon, France.ORCID 0000-0002-9777-0866
Christophe LouvetDepartment of Medical Oncology, Institut Mutualiste Montsouris, Paris, France.
Celine LepereDepartment of Gastroenterology and Gastrointestinal Oncology, CARPEM Comprehensive Cancer Center, Georges-Pompidou European Hospital, AP-HP, Paris, France.
Jean Francois EmileLaboratory of Integrative Cancer Immunology, Equipe Labellisée Ligue Contre le Cancer, Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université Paris Cité, Paris, France.ORCID 0000-0002-6073-4466
Olivier BoucheDepartment of Digestive Oncology, Hospital Robert Debré, Reims, France.ORCID 0000-0002-8284-3743
Thibault MazardDepartment of Medical Oncology, Montpellier Cancer Institute (ICM), Institut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, University of Montpellier, Montpellier, France.
Dewi VernereyMethodology and Quality of Life in Oncology Unit, Besançon University Hospital, Besançon, France.
Konstantinos VogiatzoglouLaboratory of Translational Oncology, Medical School, University of Crete, Heraklion, Greece.
Maria TzardiLaboratory of Pathology, University Hospital of Heraklion, Crete, Greece.
Shruti SharmaNatera, Inc, Austin, TX.
Minetta C LiuNatera, Inc, Austin, TX.ORCID 0000-0002-8206-5232
Himanshu SethiNatera, Inc, Austin, TX.
Thierry AndréSorbonne Université, Paris, France.ORCID 0000-0002-5103-7095
Jérome GalonLaboratory of Integrative Cancer Immunology, Equipe Labellisée Ligue Contre le Cancer, Centre de Recherche des Cordeliers, INSERM, SIRIC CARPEM, Sorbonne Université, Université Paris Cité, Paris, France.ORCID 0000-0001-9635-1339
Pierre Laurent-PuigCentre de Recherche des Cordeliers, INSERM, CNRS, Université Paris-Cité, Sorbonne Université, USPC, Equipe labellisée Ligue Nationale Contre le Cancer, Paris, France.ORCID 0000-0001-8475-5459

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeImmunoscore (IS) and circulating tumor DNA (ctDNA) are two emerging technologies in improving prognostication and tailoring adjuvant treatments in patients resected from a stage III colon cancer (CC). Here, we analyzed the prognostic value of the two biomarkers in patients who participated in the randomized phase III IDEA-France and HORG trials.

methodsPlasma samples were collected after surgery and before adjuvant chemotherapy. ctDNA analysis was performed using a clinically validated, personalized, tumor-informed 16-plex protein chain reaction assay. Multivariable analyses for time to recurrence (TTR; patients without recurrence or death due to CC) and overall survival (OS) were performed using ctDNA and IS results, along with other parameters including treatment duration and disease risk group.

resultsOf the 554 patients with available ctDNA results, 445 were ctDNA-negative (80.3%) and 109 were ctDNA-positive (19.7%); baseline characteristics showed more T4/N2 and venous embolism/lymphatic invasion/perineural invasion+ in ctDNA-positive patients. With a median follow-up of 6.7 years, the 2-year TTR rate was 43.5% (95% CI, 34.1 to 52.6) for ctDNA-positive patients and 88.1% (95% CI, 84.7 to 90.8) for ctDNA-negative patients (

conclusionIn this combined analysis of two adjuvant trials dedicated to patients with stage III CC after surgery, ctDNA was detectable in 19.7% of the patients and was confirmed as a major independent prognostic biomarker. IS seems to bring additional prognostic information in the 80.3% of patients who are ctDNA-negative.

Indexed as

Biomarkers, TumorCirculating Tumor DNAColonic NeoplasmsAdultAgedChemotherapy, AdjuvantFemaleFranceHumansMaleMiddle AgedNeoplasm StagingPrognosisBiomarkers, TumorCirculating Tumor DNA

Identifiers

PMID39903903
PMCPMC12054978

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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.