Evidence map›Paper›PMID 41976325›Full record

ArticleCancers2026

Feasibility of

Regine Marlin, Mehdi Jean-Laurent, Clarisse Joachim, Alexis Vallard, Sabrina Pennont, Valerie Suez-Panama, Mickaelle Rose, Sylviane Ulric-Gervaise, Sylvie Lusbec, Odile Bera and 2 more

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Regine MarlinPôle de Biologie, Génétique des Cancers, CHU de Martinique, Fort-de-France, 97200 Martinique, France.ORCID 0000-0001-7580-2997
Mehdi Jean-LaurentPole MFME, Chirurgie Gynécologique et Mammaire, CHU de Martinique, Fort-de-France, 97200 Martinique, France.
Clarisse JoachimPôle de Cancérologie Hématologie Urologie, Registre Général des Cancers de la Martinique, CHU de Martinique, Fort-de-France, 97200 Martinique, France.
Alexis VallardPôle de Cancérologie Hématologie Urologie, CHU de Martinique, Fort-de-France, 97200 Martinique, France.
Sabrina PennontPôle de Biologie, Génétique des Cancers, CHU de Martinique, Fort-de-France, 97200 Martinique, France.
Valerie Suez-PanamaPôle de Biologie, Centre de Ressources Biologiques, CHU de Martinique, Fort-de-France, 97200 Martinique, France.
Mickaelle RosePlateforme Régionale d'Oncologie de Martinique (GIP PROM), CHU de Martinique, Fort-de-France, 97200 Martinique, France.ORCID 0000-0001-7563-513X
Sylviane Ulric-GervaisePôle de Biologie, Génétique des Cancers, CHU de Martinique, Fort-de-France, 97200 Martinique, France.
Sylvie LusbecPole MFME, Chirurgie Gynécologique et Mammaire, CHU de Martinique, Fort-de-France, 97200 Martinique, France.
Odile BeraPôle de Biologie, Génétique des Cancers, CHU de Martinique, Fort-de-France, 97200 Martinique, France.
Aude Aline-FardinPôle de Biologie, Anatomopathologie, CHU de Martinique, Fort-de-France, 97200 Martinique, France.
Coralie EbringPole MFME, Chirurgie Gynécologique et Mammaire, CHU de Martinique, Fort-de-France, 97200 Martinique, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesHigh-grade endometrial cancer (EC) is associated with poor outcomes, particularly in populations with a high burden of aggressive histologies. There is a critical need for accessible biomarkers to improve prognostic assessment and guide clinical management.

methodsIn this study, we evaluated the feasibility and clinical relevance of monitoring circulating tumor DNA (ctDNA) by tracking somatic

resultsAmong 21 patients with high-grade EC carrying

conclusionsThese findings highlight the potential role of ctDNA as a real-time molecular marker of minimal residual disease and tumor dynamics. Our results demonstrate that

Indexed as

ctDNA monitoringhigh-grade endometrial cancerliquid biopsyminimal residual diseasenext-generation sequencingrecurrence detectionTP53 mutation

Identifiers

PMID41976325
PMCPMC13072404

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.