Evidence map›Paper›PMID 37752419›Full record

ArticleBMC cancer2023

IDH mutations in G2-3 conventional central bone chondrosarcoma: a mono institutional experience.

Elisabetta Setola, S Benini, A Righi, G Gamberi, E Carretta, C Ferrari, S Avnet, E Palmerini, G Magagnoli, M Gambarotti and 10 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 19% of its field
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

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Isocitrate dehydrogenase mutations as potential tumour agnostic targets.EJC supplements : EJC : official journal of EORTC, European Organization for Research and Treatment of Cancer ... [et al.] · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Diagnostics ofDiagnostics (Basel, Switzerland) · 2024
    Article
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

20 authors at 2 institutions in 1 country.

Elisabetta SetolaOsteoncology, Bone and Soft Tissue Sarcomas and Innovative Therapies, IRCCS Istituto Ortopedico Rizzoli, Via Pupilli 1, Bologna, 40136, Italy. elisabetta.setola@ieo.it.
S BeniniDepartment of Pathology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
A RighiDepartment of Pathology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
G GamberiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
E CarrettaIRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
C FerrariExperimental Oncology Laboratory, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
S AvnetDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
E PalmeriniOsteoncology, Bone and Soft Tissue Sarcomas and Innovative Therapies, IRCCS Istituto Ortopedico Rizzoli, Via Pupilli 1, Bologna, 40136, Italy.
G MagagnoliDepartment of Pathology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
M GambarottiDepartment of Pathology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
P L LolliniDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
M CesariOsteoncology, Bone and Soft Tissue Sarcomas and Innovative Therapies, IRCCS Istituto Ortopedico Rizzoli, Via Pupilli 1, Bologna, 40136, Italy.
S CocchiDepartment of Pathology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
A PaioliOsteoncology, Bone and Soft Tissue Sarcomas and Innovative Therapies, IRCCS Istituto Ortopedico Rizzoli, Via Pupilli 1, Bologna, 40136, Italy.
A LonghiOsteoncology, Bone and Soft Tissue Sarcomas and Innovative Therapies, IRCCS Istituto Ortopedico Rizzoli, Via Pupilli 1, Bologna, 40136, Italy.
K ScotlandiExperimental Oncology Laboratory, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
M A LaginestraExperimental Oncology Laboratory, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
D M DonatiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
N BaldiniDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
T IbrahimOsteoncology, Bone and Soft Tissue Sarcomas and Innovative Therapies, IRCCS Istituto Ortopedico Rizzoli, Via Pupilli 1, Bologna, 40136, Italy.
Istituto Ortopedico Rizzoli · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeterozygous isocitrate dehydrogenase (IDH) mutations occur in about half of conventional central bone chondrosarcomas (CCBC). Aim of this study was to assess the frequency and prognostic impact of IDH mutations in high grade CCBC patients.

methods64 patients with G2 and G3 CCBC were included. DNA extraction, PCR amplification of IDH1/2 exon 4s, and sequencing analysis with Sanger were performed.

resultsIDH mutations were detected in 24/54 patients (44%): IDH1 in 18, IDH2 in 4, and both IDH1/2 in 2 patients. The frequency of mutations was 37% in G2 vs. 69% in G3 (p = 0.039), and 100% in three Ollier disease associated chondrosarcoma. 5-year overall survival (OS) at 124 months (range 1-166) was 51%, with no significant difference based on the IDH mutational status: 61% in IDHmut vs. 44% in IDH wild type (IDHwt). The 5-year relapse free survival (RFS) was 33% (95% CI:10-57) for IDHmut vs. 57% (95%CI: 30-77) for IDHwt. Progression free survival (PFS) was 25% (95%CI:1-65) IDHmut vs. 16% (95%CI: 0.7-52) IDHwt. 55% (5/9) of IDHmut G2 became higher grade at the recurrence, as compared with 25% (3/12) of G2 IDHwt.

conclusionsThis study shows a higher frequency of IDH mutations in G3 CCBC as compared with G2. No significant differences in OS, RFS, and PFS by mutational status were detected. After relapse, a higher rate of G3 for IDH mutated CCBC was observed.

Indexed as

Bone NeoplasmsChondrosarcomaExonsHumansIsocitrate DehydrogenaseMutationIsocitrate DehydrogenaseBone sarcomacancer metabolismChondrosarcomaIDH inhibitorsIDH mutationPrognostic factorsSarcomaTarget therapy

Identifiers

PMID37752419
PMCPMC10521511
OpenAlexW4387052412

What OpenQuestion holds

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LicenceCC BY
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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.