Evidence map›Paper›PMID 41650748›Full record

ArticleESMO open2026

Activity of chemotherapy in mesenchymal chondrosarcoma: a multicentre retrospective analysis within the Italian Sarcoma Group network.

G G Baldi, A M Frezza, C Biagioni, M Benelli, S Bazzurri, M Cesari, G Bianchi, D Greto, D A Campanacci, S Aliberti and 15 more

Abstract read
In one paragraph

Article in ESMO open, 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

25 authors.

G G BaldiDepartment of Medical Oncology, Hospital of Prato, Prato, Italy. Electronic address: giacomogiulio.baldi@uslcentro.toscana.it.
A M FrezzaDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
C BiagioniDepartment of Medical Oncology, Hospital of Prato, Prato, Italy.
M BenelliDepartment of Experimental and Clinical Biomedical Sciences 'Mario Serio', University of Florence, Florence, Italy.
S BazzurriDepartment of Medical Oncology, Hospital of Prato, Prato, Italy.
M CesariOsteoncology, Bone and Soft Tissue Sarcomas and Innovative Therapies Unit, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
G BianchiDepartment of Orthopedic Oncology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
D GretoDepartment of Radiotherapy, Azienda Ospedaliero Universitaria Careggi, University of Florence, Florence, Italy.
D A CampanacciDepartment of Orthopaedic Oncology, Azienda Ospedaliero Universitaria Careggi, University of Florence, Florence, Italy.
S AlibertiDepartment of Medical Oncology, Sarcoma Unit, Candiolo Cancer Institute FPO, IRCCS, Candiolo (Turin), Italy.
G M MilanoDivision of Hematology/Oncology, Cellular and Gene Therapy, Ospedale Pediatrico Bambino Gesù IRCCS, Rome, Italy.
N PumaPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
B VincenziDepartment of Medical Oncology, Università Campus Bio-Medico di Roma, Rome, Italy.
A BrunelloDepartment of Oncology, Medical Oncology 1 Unit, Istituto Oncologico Veneto IOV-IRCCS, Padua, Italy.
S D AsafteiDepartment of Pediatric Hematology/Oncology, 'Regina Margherita' Children's Hospital, AOU Città della Salute e della Scienza, Turin, Italy.
R M KelaneyDepartment of Oncology, Ain Shams University, Cairo, Egypt.
M GambarottiDepartment of Pathology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
P ColliniDepartment of Advanced Diagnostics, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
A FranchiSection of Pathology, Department of Translational Research and of New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
M SbaragliaDepartment of Pathology, Azienda Ospedaliero Universitaria, University of Padua, Padua, Italy.
G P DagradaDepartment of Advanced Diagnostics, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
C MorosiDepartment of Radiology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
A GronchiDepartment of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
P G CasaliDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
S StacchiottiDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal chondrosarcoma (MCS) is an ultra-rare sarcoma, molecularly defined by the HEY1::NCOA2 fusion, and characterized by a poor prognosis in the advanced phase. Data on the activity of systemic agents in MCS are only retrospective and limited to case reports or heterogeneous series. We report the results of an Italian, multicentric, retrospective study on the activity of cytotoxic chemotherapy in patients with MCS. PATIENTS AND

methodsThis retrospective, multicentre Italian Sarcoma Group study included patients with molecularly confirmed MCS, treated with anthracycline-based chemotherapy, high-dose ifosfamide (HD-IFX), or trabectedin between 2000 and 2022. Response to treatment was assessed retrospectively through imaging review. Survival outcomes were estimated by the Kaplan-Meier method.

resultsThirty-five patients were identified (19 = localized disease, 16 = advanced disease). Anthracycline-based regimens yielded an overall response rate (ORR) of 26% [95% confidence interval (CI) 15% to 50%]. Among patients with localized disease, Ewing-like regimens showed an ORR of 33.3% (95% CI 9.9% to 65.1%), median relapse-free survival (mRFS) of 86.9 months, and 5-year overall survival of 95%; other anthracycline combinations had an ORR of 40% (95% CI 5.3% to 85.3%) and mRFS of 32.6 months. In advanced disease, Ewing-like regimens yielded an ORR of 16.7% (95% CI 0.4% to 64.1%) and median progression-free survival (mPFS) of 13.2 months, while other anthracycline regimens resulted in an ORR of 22.2% (95% CI 15% to 50%) and mPFS of 9.3 months. HD-IFX showed no responses, with early progression in all cases. Trabectedin achieved stable disease in all four treated patients, with a median PFS of 16.9 months.

conclusionsThis multicentre study confirms that anthracycline-based regimens show activity in MCS, with responses more in line with soft tissue sarcoma than Ewing sarcoma. Their benefit in localized disease remains uncertain, but (neo)adjuvant chemotherapy with Ewing-like regimens should be considered for patients eligible for surgery. In advanced disease, trabectedin may provide prolonged disease control after anthracyclines.

Indexed as

anthracyclinesbone sarcomachondrosarcomasoft-tissue sarcomatrabectedinultra-rare sarcomas

Identifiers

PMID41650748
PMCPMC12919272

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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.