Evidence map›Paper›PMID 42237063›Full record

Observational studyCancer medicine2026

Metastatic Ewing Sarcoma, Patterns of Care and Outcomes of Patients in a Real-Life National Setting Over a Decade.

Coline Ducrot, Derek Dinart, Maeva Bonneau, Max Piffoux, Marie Sophie Minot, Juliane Mignot-Posson, Thomas Grinda, Jordane Chaix, Sarah Winter, Pauline Gerard and 15 more

Erratum issuedAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors.

Coline DucrotCentre Léon Bérard, Lyon, France.
Derek DinartInstitut Bergonié, Bordeaux, France.
Maeva BonneauInstitut Universitaire du Cancer de Toulouse, Oncopole, France.
Max PiffouxCentre Léon Bérard, Lyon, France.
Marie Sophie MinotCentre Hospitalier Universitaire Cochin, APHP, Paris, France.ORCID 0000-0002-9693-9850
Juliane Mignot-PossonCentre Hospitalier Universitaire de Nantes, Nantes, France.
Thomas GrindaInstitut Gustave Roussy, Villejuif, France.
Jordane ChaixCentre Hospitalier Universitaire Pellegrin, Bordeaux, France.ORCID 0000-0002-4482-0065
Sarah WinterInstitut Curie, Paris, France.
Pauline GerardHôpitaux Universitaires de Strasbourg, Strasbourg, France.
Romain DuongCentre Hospitalier Régional Universitaire de Tours, Tours, France.
Berengère NarcisoCentre Hospitalier Régional Universitaire de Tours, Tours, France.
Natacha Entz-WerleHôpitaux Universitaires de Strasbourg, Strasbourg, France.
Cécile VéritéCentre Hospitalier Universitaire Pellegrin, Bordeaux, France.
Valérie LaurenceInstitut Curie, Paris, France.
Axel Le CesneInstitut Gustave Roussy, Villejuif, France.
Pablo BerlangaInstitut Gustave Roussy, Villejuif, France.ORCID 0000-0003-1110-7789
Camille TlemsaniCentre Hospitalier Universitaire Cochin, APHP, Paris, France.
Pascaline Boudou-RouquetteCentre Hospitalier Universitaire Cochin, APHP, Paris, France.
Emmanuelle BompasInstitut de Cancérologie de L'ouest, Saint-Herblain, France.
Thibaud ValentinInstitut Universitaire du Cancer de Toulouse, Oncopole, France.
Nadège CorradiniCentre Léon Bérard, Lyon, France.
Mehdi BrahmiCentre Léon Bérard, Lyon, France.
Carine BelleraInstitut Bergonié, Bordeaux, France.
Maud ToulmondeInstitut Bergonié, Bordeaux, France.

Funding

BayerInstitut National Du Cancer
6 · The paper itself

Abstract

Metastatic Ewing sarcoma (MES) has a poor prognosis. This multicenter observational study provides real-world data on treatment patterns of patients with MES in France. Treatment characteristics, outcomes such as time to next treatment (TTNT) and overall survival (OS), and prognostic factors of patients aged ≥ 12 years treated for a MES in 11 French reference network centers were retrieved from our national database. From 2008 to 2018, 156 patients with MES were included: 82 were metastatic at diagnosis (upfront metastatic cohort), 74 had developed secondary metastases after treatment of a localized disease (metastatic relapse cohort). 94% of patients received systemic treatment, with a median of three lines (1-11), 61% had at least one loco-regional procedure and 42% of patients participated in a clinical trial in the metastatic setting. Median OS from metastatic diagnosis was 20.3 months [95% CI 14.0; 27.7] in the metastatic relapse cohort and 31.4 months [95% CI 26.5; 42.5] in the upfront metastatic cohort (p = 0.02). Median TTNT in first metastatic line was 16.8 months [95% CI 12.9; 21.3] in the upfront metastatic cohort and 7.4 months [95% CI 5.0; 11.1] in the metastatic relapse cohort, 5.8 months [95% CI 3.6; 7.3] in 2nd line and 3.8 months [95% CI 2.8; 5.7] in 3rd line, without significant difference between cohorts and treatment regimens. Patients with upfront MES have a longer OS than patients with relapsing disease, mainly due to first metastatic line dose-dense polychemotherapy and loco-regional procedures in selected patients. Main regimens used at relapse are associated with the same range of benefit and survival, while TKIs such as regorafenib or cabozantinib have modest activity. Inclusion in clinical trials should be prioritized.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBone NeoplasmsSarcoma, EwingAdolescentAdultChildFemaleFranceHumansMaleMiddle AgedNeoplasm MetastasisPrognosisTreatment OutcomeYoung Adultchemotherapyclinical trialsloco‐regional treatmentmetastatic Ewing sarcomaprognostic factorssurvivalsystemic treatmenttime to next treatmenttyrosine kinase inhibitors

Identifiers

PMID42237063
PMCPMC13240556

What OpenQuestion holds

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LicenceCC BY-NC
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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.