Evidence map›Paper›PMID 42525308›Full record

ReviewCurrent treatment options in oncology2026

Dedifferentiated Chondrosarcoma: Current Advances and Future Perspectives.

Rebecca Ibrahim, Julien Vibert, Tania Moussa, Carine Ngo, Matthieu Faron, Benjamin Verret, Caterina Zanella, Rabih Mikhael, Elie Tabet, Antonin Lévy and 5 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 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

15 authors.

Rebecca IbrahimDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Julien VibertDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Tania MoussaRadiology Department, Gustave Roussy, Université Paris Saclay, 114 Rue Edouard Vaillant, Villejuif, 94805, France.
Carine NgoDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Matthieu FaronDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Benjamin VerretDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Caterina ZanellaDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Rabih MikhaelDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Elie TabetDepartment of Neurology, Massachussets General HospitalHarvard Medical School, Boston, MA, 02129, USA.
Antonin LévyDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Charles HonoréDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Cécile Le PéchouxDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Ratislav BahledaDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Axel Le CesneDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France.
Tarek AssiDepartment of Cancer Medicine, Gustave Roussy, Villejuif, France. tarek.assi@gustaveroussy.fr.ORCID https://orcid.org/0000-0002-5579-5264

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementDedifferentiated chondrosarcoma (DDCS) remains one of the most aggressive and therapeutically challenging primary bone malignancies. While surgery continues to represent the cornerstone of treatment for localized disease, outcomes remain poor due to high rates of local recurrence and metastatic progression. The role of adjuvant therapies remains less clear. Radiotherapy may be considered in selected patients with unresectable tumors, positive margins, or for symptom palliation, whereas conventional chemotherapy has demonstrated inconsistent and generally limited benefit despite the use of osteosarcoma-based regimens. Recent advances in molecular profiling have improved our understanding of DDCS biology and revealed potential therapeutic opportunities. Recurrent IDH1/2 mutations appear to contribute to tumor progression and dedifferentiation and may represent actionable therapeutic targets. In our practice, comprehensive molecular profiling should be considered whenever feasible, particularly in advanced disease. Emerging evidence suggests that immunotherapy can induce durable responses in a small subset of patients, while early studies combining immune checkpoint inhibitors with antiangiogenic tyrosine kinase inhibitors have demonstrated encouraging response rates that exceed those historically achieved with chemotherapy alone. Although these findings require prospective validation, they support a shift toward biomarker-driven and combination treatment strategies.

Indexed as

Bone NeoplasmsChondrosarcomaBiomarkers, TumorCombined Modality TherapyDisease ManagementHumansImmunotherapyIsocitrate DehydrogenaseMolecular Targeted TherapyMutationPrognosisTreatment OutcomeBiomarkers, TumorIsocitrate DehydrogenaseChemotherapyChondrosarcomaImmunotherapyMesenchymalSarcomaTargeteted therapy

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.