Evidence map›Paper›PMID 39379569›Full record

Trial reportBritish journal of cancer2024

Role of

Nina Jehanno, Nadège Corradini, Nathalie Gaspar, Mehdi Brahmi, Thibaud Valentin, Gabriel Revon Rivière, Cyril Lervat, Jamie Probert, Natacha Entz-Werle, Ludovic Mansuy and 11 more

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

Trial report in British journal of cancer, 2024. 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

21 authors.

Nina JehannoDepartment of Nuclear Medicine, Curie Institute, Paris, France. nina.jehanno@curie.fr.ORCID http://orcid.org/0000-0002-4370-8223
Nadège CorradiniDepartment of Pediatric Oncology, Institute for Paediatric Haematology and Oncology, Léon Bérard Center, Lyon, France.
Nathalie GasparDepartment of Oncology for Child and Adolescent, Gustave Roussy Cancer Campus, Villejuif, France.ORCID http://orcid.org/0000-0002-1827-8903
Mehdi BrahmiDepartment of Medical Oncology, Léon Bérard Center, 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 Oncology, CHU, Strasbourg, France.
Ludovic MansuyChildren's University Hospital, Department of Pediatric Hematology and Oncology, Nancy, France.
Dominique PlantazDepartment of Pediatric Hematology and Oncology, University Hospital of Grenoble, Grenoble, France.
Maria RiosInstitut de Cancérologie de Lorraine-Alexis Vautrin, Vandoeuvre-lès-Nancy, France.
Laure SaumetDepartment of Pediatric Onco-Hematology, University Hospital of Montpellier, Montpellier, France.
Cécile VeritéDepartment 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.
Veronique MosseriDepartment of Biostatistics, Curie Institut, Saint-Cloud, 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.
Valerie 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.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Ewing Sarcoma Family of Tumors (ESFT) constitutes a group of rare malignancies, wherein approximately one-third of cases exhibit metastatic spread, particularly impacting prognosis when bone and/or bone marrow (BM) are involved. Primary extra-pulmonary metastatic ESFT often necessitates intensified therapeutic approaches. Accurate staging plays a pivotal role in clinical decision-making, with fluorine-18-fluorodeoxyglucose-positron emission tomography/computed tomography (PET/CT) currently serving as a non-invasive modality for assessing ESFT's BM extent.

methodsIn the French phase II COMBINAIR3 (NCT03011528) study, a comprehensive approach for patients with extra-pulmonary ESFT metastasis was evaluated. We prospectively compared the efficacy of PET/CT to BM aspiration and biopsy (BMAB) analysis in patients undergoing initial staging.

resultsAmong the 42 patients analyzed (median age 14 y, 2:1 male/female ratio), 45% presented with pelvic primary tumors and 83% had bone/BM involvement at diagnosis. Our findings showed PET/CT had 100% specificity and 83.3% sensitivity in detecting initial BM involvement. Overall, PET/CT correctly classified 92.8% of patients, reaching 100% accuracy in patients identified with bone involvement, thus surpassing the standard BMAB. DISCUSSION: These results suggest that the conventional use of BMAB in the initial staging of high-risk ESFT patients can be omitted, promoting PET/CT as a non-invasive alternative, thus improving staging accuracy and treatment decisions in ESFT management.

Indexed as

Bone MarrowBone NeoplasmsFluorodeoxyglucose F18Neoplasm StagingPositron Emission Tomography Computed TomographySarcoma, EwingAdolescentAdultChildFemaleHumansMaleProspective StudiesRadiopharmaceuticalsYoung AdultFluorodeoxyglucose F18Radiopharmaceuticals

Identifiers

PMID39379569
PMCPMC11554785

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.