Evidence map›Paper›PMID 42556071›Full record

ReviewCancer treatment reviews2026

Chondrosarcoma: A comprehensive review of tumor biology, clinical behavior, and therapeutic advances.

Luyuan Li, Genevieve Bertolet, Josiane E Eid, William D Tap, Andrew J Wagner, Anthony P Conley, Francis J Hornicek, Zhenfeng Duan, Emanuela Palmerini, Jonathan C Trent

Abstract readReview
In one paragraph

Review in Cancer treatment reviews, 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

10 authors.

Luyuan LiDepartment of Medicine, North Alabama Medical Center, Florence, AL 35630, United States; Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL 33136, United States. Electronic address: luyuanlidr@gmail.com.
Genevieve BertoletThe University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.
Josiane E EidSylvester Comprehensive Cancer Center, University of Miami, Miami, FL 33136, United States.
William D TapMemorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY 10065, United States.
Andrew J WagnerDana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, United States.
Anthony P ConleyThe University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.
Francis J HornicekSylvester Comprehensive Cancer Center, University of Miami, Miami, FL 33136, United States.
Zhenfeng DuanSylvester Comprehensive Cancer Center, University of Miami, Miami, FL 33136, United States.
Emanuela PalmeriniSylvester Comprehensive Cancer Center, University of Miami, Miami, FL 33136, United States.
Jonathan C TrentSylvester Comprehensive Cancer Center, University of Miami, Miami, FL 33136, United States. Electronic address: jtrent@med.miami.edu.

Funding

Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Stephen D. Nimer · 2019 to 2026
$24.1M
NCI NIH HHS P30 CA240139
6 · The paper itself

Abstract

Chondrosarcoma is a heterogeneous group of malignant bone tumors characterized by the production of neoplastic hyaline cartilage. These tumors are often indolent and typically resistant to conventional chemotherapy and radiotherapy, with surgical resection remaining the cornerstone of treatment. However, patients with unresectable or metastatic disease face poor outcomes due to the lack of effective systemic therapies. While advancements in systemic treatments - such as immunotherapy and anti-angiogenic agents - and novel radiation modalities like proton beam therapy and carbon ion therapy have shown some benefit in select cases, their overall efficacy remains limited, underscoring the urgent need for more effective treatment options. Emerging novel therapies are beginning to illuminate potential new treatment pathways. Current efforts are increasingly focused on targeting recurrent genetic alterations and dysregulated signaling pathways, including IDH mutations, DR5-mediated apoptotic pathway, hedgehog signaling, Src kinase pathway, the PI3K-Akt-mTOR axis, histone deacetylation, and angiogenesis. Although these targeted strategies are still under investigation, they show promise in overcoming therapeutic resistance and advancing personalized treatment. This review provides an overview of the clinical characteristics of major chondrosarcoma subtypes, key genetic alterations implicated in tumor pathogenesis, and recent advances in treatment strategies, including surgery, chemotherapy, radiotherapy, immunotherapy, and emerging targeted therapies.

Indexed as

Bone NeoplasmsChondrosarcomaHumansImmunotherapyMolecular Targeted TherapySignal TransductionChemo-radiotherapy resistanceChondrosarcomaIDH mutationImmunotherapySurgical resectionTargeted therapy

Identifiers

PMID42556071
PMCPMC13640447

What OpenQuestion holds

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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.