Evidence map›Paper›PMID 41808443›Full record

ArticleActa oncologica (Stockholm, Sweden)2026

Characteristics, treatment and survival of patients with chondrosarcoma in five European countries: a DARWIN EU® cohort study.

Anton Barchuk, Cesar Barboza, Julieta Politi, Berta Raventós, Peter Prinsen, Jelle Evers, Vincent Ky Ho, Michiel Aj Van de Sande, Eric Fey, Kimmo Porkka and 18 more

Abstract readMulticenter Study
In one paragraph

Article in Acta oncologica (Stockholm, Sweden), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

28 authors.

Anton BarchukDepartment of Medical Informatics, Erasmus Medical Center, Rotterdam, Netherlands; University of Helsinki, Helsinki, Finland. a.barchuk@erasmusmc.nl.ORCID 0000-0002-4629-3326
Cesar BarbozaDepartment of Medical Informatics, Erasmus Medical Center, Rotterdam, Netherlands.ORCID 0009-0002-4453-3071
Julieta PolitiDepartment of Medical Informatics, Erasmus Medical Center, Rotterdam, Netherlands.ORCID 0000-0001-7315-034X
Berta RaventósDepartment of Medical Informatics, Erasmus Medical Center, Rotterdam, Netherlands.ORCID 0000-0002-4668-2970
Peter PrinsenNetherlands Comprehensive Cancer Organisation (IKNL), Utrecht, The Netherlands.ORCID 0000-0002-0444-4579
Jelle EversNetherlands Comprehensive Cancer Organisation (IKNL), Utrecht, The Netherlands.ORCID 0000-0003-0525-9786
Vincent Ky HoNetherlands Comprehensive Cancer Organisation (IKNL), Utrecht, The Netherlands.ORCID 0000-0001-7065-928X
Michiel Aj Van de SandeOrthopedic Surgery, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-9156-7656
Eric FeyiCAN Digital Precision Cancer Medicine Flagship, University of Helsinki and Helsinki University Central Hospital Cancer Center, Helsinki, Finland.ORCID 0009-0005-7847-7479
Kimmo PorkkaiCAN Digital Precision Cancer Medicine Flagship, University of Helsinki and Helsinki University Central Hospital Cancer Center, Helsinki, Finland.ORCID 0000-0003-4112-5902
Anna HammaisFinnish Institute for Health and Welfare (THL), Helsinki, Finland.
Tiina WahlforsFinnish Institute for Health and Welfare (THL), Helsinki, Finland.ORCID 0000-0002-3910-796X
Tuomo NieminenFinnish Institute for Health and Welfare (THL), Helsinki, Finland.ORCID 0000-0002-6901-2208
Toni LehtonenFinnish Institute for Health and Welfare (THL), Helsinki, Finland.ORCID 0000-0003-2089-2299
Antonella DelmestriCentre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology, and Musculoskeletal Sciences (NDORMS), University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-0388-3403
Guillaume VerdyPublic Health Department, Medical Information Service, University Hospital of Bordeaux, Bordeaux, France.ORCID 0000-0002-0745-0034
Romain GriffierPublic Health Department, Medical Information Service, University Hospital of Bordeaux, Bordeaux, France.ORCID 0000-0002-1096-137X
Airam De Burgos-GonzálezAgencia Española de Medicamentos y Productos Sanitarios, Madrid, Spain.ORCID 0000-0002-4928-0491
Ana Llorente-GarciaAgencia Española de Medicamentos y Productos Sanitarios, Madrid, Spain.
Cristina Justo-AstorganoAgencia Española de Medicamentos y Productos Sanitarios, Madrid, Spain.
Miguel-Angel Macia-MartinezAgencia Española de Medicamentos y Productos Sanitarios, Madrid, Spain.ORCID 0000-0002-1471-4376
Olli TenhunenMedical Research Center Oulu, Oulu University Hospital, University of Oulu, Oulu, Finland; Finnish Medicines Agency, Helsinki, Finland.ORCID 0009-0009-0802-1619
Anja SchielNorwegian Medical Products Agency (NOMA), Oslo, Norway.ORCID 0000-0002-1258-4731
Alexandra PacurariuReal World Evidence Workstream, European Medicines Agency, Amsterdam, The Netherlands.ORCID 0000-0002-2217-0540
Ross BrennanReal World Evidence Workstream, European Medicines Agency, Amsterdam, The Netherlands.
Ross WilliamsDepartment of Medical Informatics, Erasmus Medical Center, Rotterdam, Netherlands.ORCID 0000-0001-7723-417X
Katia VerhammeDepartment of Medical Informatics, Erasmus Medical Center, Rotterdam, Netherlands.ORCID 0000-0001-8162-4904
Talita Duarte SallesDepartment of Medical Informatics, Erasmus Medical Center, Rotterdam, Netherlands; Fundació Institut Universitari per a la recerca a l'Atenció Primària de Salut Jordi Gol i Gurina (IDIAPJGol), Barcelona, Spain.ORCID 0000-0002-8274-0357

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeChondrosarcoma is a rare bone malignancy with a poor response to systemic therapy in advanced stages. European-level epidemiological data remain scarce. This study aimed to characterise patient demographics, treatments and survival using real-world data to inform regulatory decisions about the feasibility and design of new trials for the systemic treatment of chondrosarcoma. Patient/material and methods: This cohort study, part of the DARWIN EU® initiative, analysed data from six healthcare databases in Finland, France, the Netherlands, Spain and the UK. Patients diagnosed with chondrosarcoma between 2010 and 2022 were identified. Standardised analyses were performed within a federated network using the Observational Medical Outcomes Partnership (OMOP) Common Data Model.

resultsA total of 2,498 chondrosarcoma patient records were identified, covering at least 2,356 unique patients. Median age at diagnosis was 52-55 years, with a balanced sex distribution. Surgical treatment was the most common intervention, recorded in 15.2% to 88.9% of patients, depending on the database. Fewer than 5% received systemic anticancer therapy, and radiotherapy was reported in fewer than 7%. The 10-year overall survival (OS) ranged from 58% (95% confidence interval [CI]: 43-78) to 80% (95% CI: 78-82), with restricted mean survival between 7.4 and 8.7 years. In the Netherlands, patients with late-stage, metastatic or high-grade disease showed significantly poorer outcomes.

interpretationThis study demonstrates the feasibility of using real-world data across Europe to describe chondrosarcoma patients. Most had early-stage, low-grade disease amenable to surgery, with limited use of systemic therapies. Survival was generally favourable, except in advanced disease. Clinical trials remain difficult due to the rarity of advanced chondrosarcoma and the lack of standards.

Indexed as

Bone NeoplasmsChondrosarcomaAdolescentAdultAgedAged, 80 and overCohort StudiesEuropeFemaleHumansMaleMiddle AgedNetherlandsSurvival RateYoung Adult

Identifiers

PMID41808443
PMCPMC12988406

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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.