Evidence map›Paper›PMID 39934735›Full record

Observational studyBMC cancer2025

The PENDOR study: establishment of a panel of patient-derived tumor organoids from endometrial cancer to assess efficacy of PARP inhibitors.

Gwenn Le Gall, François Cherifi, Jordane Divoux, Romane Florent, François Christy, Alexandra Leconte, Chankannira San, Amélie Devillers, Guillaume Desmartin, Lucie Lecouflet and 19 more

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06603506 (Collection of Endometrial Cancer-derived Organoids to Evaluate the Efficacy of PARP Inhibitors), which is not on this 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.

NCT06603506 recruitingnot on this map

Collection of Endometrial Cancer-derived Organoids to Evaluate the Efficacy of PARP Inhibitors: PENDOR Pilot Study

TypeobservationalSponsorCentre Francois BaclesseRan2024 to 2027Enrolled16ConditionsEndometrial CancerArmstumour and blood samples
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  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

29 authors.

Gwenn Le Gall *INSERM U1086 ANTICIPE (Interdisciplinary Research Unit for Cancers Prevention and Treatment), BioTICLA Laboratory (Precision Medicine for Ovarian Cancers), Université de Caen Normandie, Caen, France.
François Cherifi *Clinical Research Department, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Jordane DivouxINSERM U1086 ANTICIPE (Interdisciplinary Research Unit for Cancers Prevention and Treatment), BioTICLA Laboratory (Precision Medicine for Ovarian Cancers), Université de Caen Normandie, Caen, France.
Romane FlorentORGAPRED core facility, US PLATON, Université de Caen Normandie, Caen, France.
François ChristyClinical Research Department, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Alexandra LeconteClinical Research Department, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Chankannira SanClinical Research Department, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Amélie DevillersClinical Research Department, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Guillaume DesmartinComprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Lucie LecoufletComprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Bénédicte ClarisseClinical Research Department, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Samantha BallestaPlateforme 3D-ONCO, Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon (CRCL) , Université Claude Bernard Lyon 1, Lyon, France.
Lucie ThorelINSERM U1086 ANTICIPE (Interdisciplinary Research Unit for Cancers Prevention and Treatment), BioTICLA Laboratory (Precision Medicine for Ovarian Cancers), Université de Caen Normandie, Caen, France.
Brice DuboisNorth-West Canceropole Data Center, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Valentin HarterNorth-West Canceropole Data Center, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Nathalie RousseauBiological Resource Center 'Tumorotheque de Caen Basse-Normandie', IRCBN Institut Régional du Cancer Basse Normandie, Caen, France.
Léopold GaichiesDepartment of Surgery, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Sandrine Martin-FrançoiseDepartment of Surgery, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Jean-François Le BrunDepartment of Surgery, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Enora DolivetINSERM U1086 ANTICIPE (Interdisciplinary Research Unit for Cancers Prevention and Treatment), BioTICLA Laboratory (Precision Medicine for Ovarian Cancers), Université de Caen Normandie, Caen, France.
Roman RouzierDepartment of Surgery, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Corinne JeanneDepartment of Biopathology, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Cécile Blanc-FournierINSERM U1086 ANTICIPE (Interdisciplinary Research Unit for Cancers Prevention and Treatment), BioTICLA Laboratory (Precision Medicine for Ovarian Cancers), Université de Caen Normandie, Caen, France.
Martin FigeacUS 41 - UAR 2014 - PLBS,CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, University of Lille, Lille, France.
Raphaël LemanDepartment of Cancer Biology and Genetics, U1245 "Cancer and brain genomics", Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Laurent CasteraDepartment of Cancer Biology and Genetics, U1245 "Cancer and brain genomics", Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France.
Laurent PoulainINSERM U1086 ANTICIPE (Interdisciplinary Research Unit for Cancers Prevention and Treatment), BioTICLA Laboratory (Precision Medicine for Ovarian Cancers), Université de Caen Normandie, Caen, France.
Louis-Bastien Weiswald *INSERM U1086 ANTICIPE (Interdisciplinary Research Unit for Cancers Prevention and Treatment), BioTICLA Laboratory (Precision Medicine for Ovarian Cancers), Université de Caen Normandie, Caen, France. lb.weiswald@baclesse.unicancer.fr.
Florence Joly *Clinical Research Department, Comprehensive Cancer Center François Baclesse, UNICANCER, Caen, France. f.joly@baclesse.unicancer.fr.

Funding

Fédération nationale des Groupements des Entreprises Françaises dans la Lutte contre le Cancer ENDOPARPLa Rochambelle PENDOR
6 · The paper itself

Abstract

backgroundCombination of chemotherapy and immunotherapy is the current standard of care for advanced endometrial cancer. However, survival outcome remains poor, highlighting the urgent need for new treatments and reliable tools to identify patients who will benefit from them. Patient-Derived Tumor Organoids (PDTO) are three-dimensional structures established from patient tumors, and are closely mimicking the features of the tumor of origin. Moreover, more and more evidences show that PTDOs hold promises as predictive tools for the response to treatment of patients.

methodThe PENDOR study is a monocentric observational study designed to assess the feasibility of generating and testing PDTOs derived from endometrial cancer for evaluating treatment sensitivity. PDTOS will be established from surgical specimens not required for anatomopathological diagnosis. Tumor cells will be dissociated, embedded in extracellular matrix, and cultured in a medium supplemented with growth factors and signaling pathways inhibitors. Molecular and histological analyses will be conducted to validate the resemblance of PDTO to the original tumor. Response of PDTO to conventional chemotherapy and PARP inhibitors will be evaluated and compared to clinical response and to the results of an academic HRD test Genomic Instability Scar (GIScar), respectively, to assess their predictive value. DISCUSSION: This pilot study aims to validate the feasibility to develop PDTOs from endometrial cancer from patients who will undergo surgical resection. We aim to provide a proof of concept regarding the predictive value of these models for their potential application into routine clinical practice as part of precision medicine. This approach could therefore facilitate the identification of patients who could benefit from PARP inhibitors.

trial registrationThis clinical trial (N°ID-RCB: 2024-A01206-41) has been validated by local research ethic committee on July 16th 2024 and registered at ClinicalTrials.gov with the identifier NCT06603506 on September 6th 2024, version 1.

Indexed as

Endometrial NeoplasmsOrganoidsPoly(ADP-ribose) Polymerase InhibitorsFemaleHumansPoly(ADP-ribose) Polymerase InhibitorsEndometrial cancerHomologous recombination deficiencyPARP inhibitorsPatient-derived tumor organoidsPredictive functional assays

Identifiers

PMID39934735
PMCPMC11817066

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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.