Evidence map›Paper›PMID 42537000›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2026

Long-Term Analysis of Patients With Ewing Sarcoma Included in the Euro-EWING99 Study.

Thibaud Valentin, Sarah Winter, Uta Dirksen, Douglas S Hawkins, Hans Gelderblom, Séverine Risbourg, Pablo Berlanga, Nathalie Gaspar, Katerine A Janeway, Heribert Juergens and 12 more

Abstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 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. [Long-term results of the euro-Ewing99-study].Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2026
    Article
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.

Thibaud ValentinOncopole Claudius Regaud, Toulouse, France.ORCID 0000-0002-3189-8445
Sarah WinterInstitut Curie, Paris, France.
Uta DirksenWest German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.ORCID 0000-0002-5435-7860
Douglas S HawkinsSeattle Children's Hospital, University of Washington, Seattle, WA.ORCID 0000-0003-3602-1375
Hans GelderblomLeiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0001-9270-8636
Séverine RisbourgCentre Oscar Lambret, Lille, France.ORCID 0009-0001-2169-9565
Pablo BerlangaGustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.ORCID 0000-0003-1110-7789
Nathalie GasparGustave Roussy Cancer Campus, Villejuif, France.ORCID 0000-0002-1827-8903
Katerine A JanewayDana-Farber/Children's Hospital Cancer Center, Boston, MA.ORCID 0000-0001-6000-3594
Heribert JuergensUniversity Children's Hospital Münster, West German Cancer Center Network, Muenster, Germany.
Ina Elisa KirchbergChildren's Hospital, University of Duisburg-Essen, Essen, Germany.ORCID 0000-0003-2529-620X
Ruth LadensteinSt Anna Children's Cancer Research Institute CCRI, Vienna, Austria.ORCID 0000-0001-6548-3873
Valérie LaurenceInstitut Curie, Paris, France.
Marie-Cécile Le DeleyCentre Oscar Lambret, Lille, France.ORCID 0000-0002-2946-4592
Martin G McCabeDivision of Cancer Sciences, University of Manchester, Manchester, United Kingdom.ORCID 0000-0002-5138-0707
Hans MerksPrincess Máxima Center, Utrecht, the Netherlands.ORCID 0000-0001-7659-1028
Andreas RanftWest German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany.ORCID 0000-0003-4424-7569
Sandra StraussUCL Cancer Institute, University College London, London, United Kingdom.ORCID 0000-0001-8328-0260
Michiel A J Van De SandeLeiden University Medical Center, Leiden, the Netherlands.
Jeremy WhelanUniversity College London Hospitals NHS Foundation Trust, London, United Kingdom.ORCID 0000-0001-6793-5722
Perrine Marec-BerardCentre Léon Bérard, Lyon, France.ORCID 0000-0001-5315-5864
Bernadette BrennanRoyal Manchester Hospital, Manchester, United Kingdom.

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

purposeEuro-EWING99 study was a large, international, prospective study recruiting patients with Ewing sarcoma (EWS) between 1999 and 2015. It assessed three different clinical questions through randomized trials. We report here the characteristics and outcomes of all patients.

methodsPatients younger than 50 years with EWS were included in the study. They received induction chemotherapy (six courses of vincristine [day 1], ifosfamide [day 1-3], doxorubicin [day 1-3], and etoposide [day 1-3; VIDE], administered every 3 weeks), local therapy (surgery/radiotherapy), and different consolidation treatments according to clinical risk group and trial.The objectives of the study were to describe the entire cohort according to the initial staging group, to describe the survival outcomes (overall survival [OS]; progression-free survival [PFS]; and local control), and to evaluate prognostic factors associated with OS and PFS.

resultsThree thousand three hundred ninety-five patients were included in the study, including 2,267 with a localized disease, 614 with pleuropulmonary metastases, and 514 with extrapulmonary metastases. Ninety-eight percent of patients received ≥4 neoadjuvant VIDE courses. The modalities of local treatment and consolidation therapy differed among the three staging groups. With a median follow-up of 7.2 years, PFS of the entire cohort was 60.2% and 55.4% at 3 and 5 years, respectively. OS was 72.6% and 64.6% at 3 and 5 years, respectively. In addition to metastatic status at diagnosis, main prognostic factors included patient age, tumor volume, and histologic response both for PFS and OS, independent of metastatic status.

conclusionTo our knowledge, this study is the largest published series of patients with EWS and may serve as a landmark paper for EWS. It confirms the major prognostic value of the complete histologic response after neoadjuvant therapy.

Identifiers

PMID42537000
PMCPMC13491399

What OpenQuestion holds

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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.