Evidence map›Paper›PMID 41249450›Full record

Trial reportBritish journal of cancer2026

Interest of a sequential multimodal approach for the treatment of newly diagnosed patients with multimetastatic Ewing sarcoma: results of the French prospective CombinaiR3 phase II trial.

Valérie Laurence, Nina Jehanno, Sylvain Dureau, Lieke Mous, Line Claude, Stelly Ballet, Gaëlle Pierron, Nathalie Gaspar, Mehdi Brahmi, Thibaud Valentin and 22 more

Registry-linked trialAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in British journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03011528 (CombinaiR3 - First-line Treatment of Ewing Tumours With Primary Extrapulmonary Dissemination in Patients From 2 to 50 Years), 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.

NCT03011528 phase2completednot on this map

CombinaiR3 - First-line Treatment of Ewing Tumours With Primary Extrapulmonary Dissemination in Patients From 2 to 50 Years

TypeinterventionalSponsorInstitut CurieRan2016 to 2023Enrolled45ConditionsEwing Sarcoma Family of TumorsArmsVDC-IE x2, VDC-IE, TEMIRI, Consolidation BuMel, Maintenance
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Long-Term Analysis of Patients With Ewing Sarcoma Included in the Euro-EWING99 Study.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
  2. Observational
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

32 authors.

Valérie LaurenceAdolescents and Young Adults Unit, Medical Oncology and SIREDO (Care, Innovation and Research for Children, Adolescents, and Young Adults with Cancer) Departments, Curie Institute, Paris, France.
Nina JehannoDepartment of Nuclear Medicine, Curie Institute, Paris, France.ORCID http://orcid.org/0000-0002-4370-8223
Sylvain DureauDepartment of Biometry, Curie Institute, Saint Cloud, France.
Lieke MousBalgrist University Hospital, Faculty of Medicine, University of Zurich (UZH), Zurich, Switzerland.
Line ClaudeDepartment of Radiation Oncology, Centre Léon Bérard, Lyon, France.
Stelly BalletGenetics Department Curie Institute & PSL Research University, Paris, France.
Gaëlle PierronGenetics Department Curie Institute & PSL Research University, Paris, France.ORCID http://orcid.org/0000-0002-2536-7680
Nathalie GasparDepartment of Oncology for Children and Adolescents, Gustave Roussy Institute, Villejuif, France.ORCID http://orcid.org/0000-0002-1827-8903
Mehdi BrahmiDepartment of Medical Oncology, Centre Léon Bérard, Lyon, France.
Thibaud ValentinDepartment of Medical Oncology, Institut Claudius Regaud, Institut Universitaire du Cancer de Toulouse - Oncopole, Toulouse, France.ORCID http://orcid.org/0000-0002-3189-8445
Gabriel Revon-RivièreDepartment of Pediatric Hematology, Immunology and Oncology, APHM - La Timone Children's Hospital, Marseille, France.
Cyril LervatDepartment of Pediatric and AYA Oncology, Centre Oscar Lambret, Lille, France.
Jamie ProbertDepartment of Pediatric Onco-hematology, University Hospital of Rennes, Rennes, France.
Natacha Entz-WerleDepartment of Pediatric Onco-hematology, University Hospitals of Strasbourg, Strasbourg, France.
Ludovic MansuyDepartment of Pediatric Hematology and Oncology, Children's University Hospital, Nancy, France.
Dominique PlantazDepartment of Pediatric Hematology and Oncology, University Hospital of Grenoble, Grenoble, France.
Maria RiosDepartment of Medical Oncology, Institut de Cancérologie de Lorraine-Alexis Vautrin, Vandoeuvre-lès-Nancy, France.
Laure SaumetDepartment of Pediatric Onco-Hematology, University Hospital of Montpellier, Montpellier, Languedoc-Roussillon, France.
Cécile VéritéDepartment of Pediatric and Adolescent Hematology and Oncology, Pellegrin Hospital, Bordeaux, France.
Marie-Pierre CastexPediatric Oncology Immunology Hematology Unit, Children's University Hospital - Toulouse University Hospital, Toulouse, France.
Estelle ThebaudDepartment of Pediatric Oncology, Hôpital Mère-Enfant, Nantes, France.
Thibaut Cassou-MounatNuclear Medicine Department, Institut Claudius Regaud, Institut Universitaire du Cancer Toulouse Oncopole, Toulouse, France.
Anne-Sophie PlissonnierDREH Pôle Promotion, Institut Curie, Saint-Cloud, France.
Jennifer DieppedaleDepartment of Biometry, Curie Institute, Saint Cloud, France.
Olivier DelattreINSERM U830, Diversity and Plasticity of Childhood Tumors Lab, SIREDO Oncology Center, Curie Institute Research Center, PSL Research University, Paris, France.
Marie-Emmanuelle LegrierDREH Pôle Promotion, Institut Curie, Saint-Cloud, France.
Perrine Marec-BérardDepartment of Pediatric Oncology, Institute for Paediatric Haematology and Oncology, Centre Léon Bérard, Lyon, France.
François GouinDepartment of Surgical Oncology, Centre Léon Bérard, Lyon, France.
Pablo BerlangaDepartment of Oncology for Children and Adolescents, Gustave Roussy Institute, Villejuif, France.
Camille CorderoAdolescents and Young Adults Unit, Medical Oncology and SIREDO (Care, Innovation and Research for Children, Adolescents, and Young Adults with Cancer) Departments, Curie Institute, Paris, France.
Didier SurdezBalgrist University Hospital, Faculty of Medicine, University of Zurich (UZH), Zurich, Switzerland.
Nadège CorradiniDepartment of Pediatric Oncology, Institute for Paediatric Haematology and Oncology, Centre Léon Bérard, Lyon, France. nadege.corradini@ihope.fr.ORCID http://orcid.org/0000-0002-1942-1222

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEwing sarcoma (ES) is a rare tumour with metastatic spread in ~25% of cases at diagnosis. Extrapulmonary disseminated disease defines very high-risk (VHR) patients, with frequent relapse and poor overall survival (OS, ~30%).

methodsThe phase II CombinaiR3 trial (NCT03011528) enroled 45 VHR ES patients across 15 French centres (2017-2021) to evaluate a strategy combining dose-dense induction chemotherapy, high-dose consolidation, and prolonged maintenance therapy. The primary endpoint was median event-free survival (EFS). Exploratory endpoints included full-body-fluorine-18-fluorodeoxyglucose-positron emission tomography/computed tomography (PET/CT) and circulating tumour DNA (ctDNA) detection during treatment.

resultsAmong 42 analysed patients (median age 14 years, range 6-47), 29 had a primary tumour volume ≥200 ml, and 35 presented with bone ± bone marrow metastatic lesions, 18 exhibiting more than 5 bone lesions. At 48-month follow-up, 18- and 36-month EFS rates were 63.4% and 53.7%, respectively, with 3-year OS at 65.5%. Toxicity was as expected, with no treatment-related deaths or maintenance therapy discontinuations due to toxicity. PET/CT and ctDNA monitoring showed strong correlation at diagnosis and relapse. DISCUSSION: This study supports the proposed experimental strategy as a first-line option for selected VHR ES patients, warranting integration into international therapeutic discussions.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBone NeoplasmsSarcoma, EwingAdolescentAdultChildCirculating Tumor DNACombined Modality TherapyFemaleFluorodeoxyglucose F18FranceHumansInduction ChemotherapyMaleMiddle AgedPositron Emission Tomography Computed TomographyCirculating Tumor DNAFluorodeoxyglucose F18

Identifiers

PMID41249450
PMCPMC12820225

What OpenQuestion holds

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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.