ChondrosarcomasNCT07315542
Diagnostic and Therapeutic Targets in Cartilaginous Tumours
An observational study of Chondrosarcomas and Cartilage Tumours, run by St. Anne's University Hospital Brno, Czech Republic at 1 site in Czechia.
Trial summary
This study, "Finding new diagnostic and therapeutic targets in cartilaginous tumours," focuses on improving the diagnosis, prognostic stratification, and treatment options for chondroid tumours, particularly chondrosarcoma. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Chondrosarcomas, Cartilage Tumours
- What is being tested?
- Tumour tissue analysis, Molecular validation and Liquid biopsy analysis
- How many people
- 300 participants
- Where
- 1 siteCzechia
- Study dates
- 1 May 2025to 31 Dec 2028
- How long will I take part?
- 5 Years
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: The study population will consist of patients with cartilaginous (chondroid) tumours treated at the First Department of Orthopaedic Surgery, St. Anne's University Hospital Brno, a national referral centre for bone tumours.
Who may be able to join
- Histologically confirmed cartilaginous (chondroid) tumour
- Diagnosis includes one of the following entities (as available and eligible):
- Enchondroma
- Atypical cartilaginous tumour / Grade 1 chondrosarcoma (ACT/G1)
- Conventional chondrosarcoma (Grade 2-3)
- Dedifferentiated chondrosarcoma
- Other rare chondrosarcoma variants (e.g., mesenchymal, clear-cell), if present in the cohort
- Patients treated and/or followed at the First Department of Orthopaedic Surgery, St. Anne's University Hospital Brno
Who cannot join
- Insufficient, degraded, or otherwise unusable tissue samples
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Czechia1 site, 1 recruiting
- Recruiting
First Department of Orthopaedic Surgery, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czechia
Brno, South Moravian, 60200
Vasileios Apostolopoulos, 722101065, Vasilis.apo@email.cz
About this study
Official title: Finding New Diagnostic and Therapeutic Targets in Cartilaginous Tumours
This study, "Finding new diagnostic and therapeutic targets in cartilaginous tumours," focuses on improving the diagnosis, prognostic stratification, and treatment options for chondroid tumours, particularly chondrosarcoma. Chondrosarcoma is the most common primary malignant bone tumour in adults and is characterized by resistance to chemotherapy and radiotherapy, making accurate diagnosis and optimal surgical management critical. Distinguishing benign cartilage tumours (enchondromas, atypical cartilaginous tumours) from low-grade chondrosarcoma, and differentiating chondrosarcoma from chondroblastic osteosarcoma, remain major diagnostic challenges.
The project investigates two key molecular markers: mutations in IDH1/2 genes and non-coding microRNAs (miRNAs). IDH1/2 mutations are frequent in central chondrosarcomas and rare in other mesenchymal tumours, making them promising diagnostic markers. Their presence may also have prognostic significance and therapeutic relevance, as IDH inhibitors are already available for other malignancies. In parallel, deregulated miRNA expression has been implicated in chondrosarcoma biology, influencing tumour growth, invasion, angiogenesis, metastasis, and chemosensitivity. Preliminary data identified distinct miRNA signatures in chondrosarcoma compared with healthy cartilage, including previously unreported miRNAs.
Read more
The study is structured into exploratory and validation phases. Global miRNA expression profiling and IDH1/2 mutation analysis will be performed using next-generation sequencing (NGS) on prospectively collected fresh-frozen tumour samples. Selected miRNAs and IDH1/2 mutation status will then be validated by RT-qPCR and targeted mutation assays in a large retrospective cohort of FFPE samples. Molecular data will be integrated with clinicopathological parameters to develop diagnostic panels capable of accurately classifying chondroid tumours, as well as prognostic miRNA panels associated with patient survival.
Additionally, the project evaluates circulating and exosomal miRNAs in liquid biopsies, aiming to establish non-invasive diagnostic and prognostic tools. Functional relevance will be explored using chondrosarcoma cell lines with simulated miRNA upregulation, coupled with transcriptomic analysis.
Overall, the study seeks to refine diagnostic accuracy, improve prognostic assessment, and identify novel molecular targets for personalized and targeted therapy in patients with inoperable or metastatic chondrosarcoma, addressing a major unmet clinical need.
Read the detailed description
The study entitled "Finding new diagnostic and therapeutic targets in cartilaginous tumours" addresses major unresolved problems in the diagnosis, prognostic assessment, and treatment of chondroid tumours, with a particular focus on chondrosarcoma. Chondrosarcoma represents approximately 30% of all primary malignant bone tumours and is the most common malignant bone sarcoma in adults. Despite its clinical relevance, the management of chondrosarcoma remains challenging due to its biological heterogeneity, resistance to chemotherapy and radiotherapy, and frequent diagnostic uncertainty, especially in low-grade lesions.
A central clinical problem lies in the differentiation between benign cartilage tumours (enchondromas and atypical cartilaginous tumours), low-grade chondrosarcoma, higher-grade chondrosarcoma, and other malignant entities such as chondroblastic osteosarcoma. Histological assessment alone is often insufficient, particularly in small biopsy specimens, and diagnostic decisions frequently rely on a subjective combination of clinical, radiological, and pathological criteria. Incorrect classification may lead either to undertreatment with insufficient local control or overtreatment with unnecessarily radical surgery. Furthermore, advanced, inoperable, or metastatic chondrosarcoma has a very poor prognosis, and effective systemic therapies are currently lacking.
This project focuses on the identification and validation of molecular biomarkers that could significantly improve diagnostic precision, prognostic stratification, and therapeutic targeting. Two main molecular areas are investigated: IDH1/2 gene mutations and non-coding microRNAs (miRNAs).
Mutations in IDH1 and IDH2 genes have been identified as characteristic molecular events in cartilaginous tumours. These mutations occur at specific amino acid residues and lead to neomorphic enzymatic activity, resulting in the production of the oncometabolite 2-hydroxyglutarate. IDH1/2 mutations are common in central chondrosarcomas and related benign precursors but are rare or absent in peripheral chondrosarcomas and other mesenchymal tumours, including osteosarcoma. As such, IDH1/2 mutation status represents a highly valuable diagnostic marker, particularly for distinguishing chondrosarcoma from chondroblastic osteosarcoma, a distinction with major therapeutic implications. The study also hypothesizes that IDH1/2 mutations may be associated with tumour aggressiveness and poorer prognosis, making them potential prognostic markers and therapeutic targets. Importantly, IDH inhibitors already used in other malignancies may represent a future treatment option for selected chondrosarcoma patients.
The second major focus of the project is the role of microRNAs, short non-coding RNAs that regulate gene expression at the post-transcriptional level. Numerous studies have shown that miRNA dysregulation contributes to tumour initiation, progression, angiogenesis, invasion, and metastasis. In chondrosarcoma, specific miRNAs have been implicated in the regulation of key oncogenic pathways, including SRC, mTOR, Wnt/β-catenin signalling, VEGF-mediated angiogenesis, and matrix remodelling. Preliminary next-generation sequencing data generated by the research team identified distinct miRNA expression profiles in chondrosarcoma compared with healthy cartilage, including several miRNAs not previously reported in the literature. These findings support the existence of tumour-specific miRNA signatures with diagnostic and prognostic potential.
The study is designed in exploratory and validation phases. In the exploratory phase, prospectively collected fresh-frozen tumour samples will undergo global miRNA expression profiling using next-generation sequencing, alongside NGS-based analysis of IDH1/2 mutation status. This phase aims to identify characteristic molecular patterns across the spectrum of chondroid tumours, including benign lesions, low-grade and high-grade chondrosarcoma, dedifferentiated variants, and chondroblastic osteosarcoma.
In the validation phase, selected deregulated miRNAs and IDH1/2 mutations will be analysed in a large retrospective cohort of FFPE samples using RT-qPCR and targeted mutation detection methods. Molecular results will be integrated with detailed clinicopathological data to develop robust diagnostic miRNA panels capable of accurately classifying chondroid tumours and distinguishing chondrosarcoma from osteosarcoma. In parallel, prognostic miRNA panels will be established and correlated with overall survival using advanced statistical methods, including Kaplan-Meier analysis and Cox proportional hazards modelling.
An innovative component of the project is the evaluation of liquid biopsies, analysing circulating and exosomal miRNAs from patient body fluids. This approach aims to establish non-invasive biomarkers for diagnosis, prognosis, and disease monitoring beyond the time of surgery. Additionally, functional relevance will be explored using chondrosarcoma cell lines, in which selected miRNAs will be experimentally upregulated to assess downstream transcriptomic effects and their relationship to IDH1/2 mutation status.
Overall, this study aims to significantly advance the understanding of chondrosarcoma biology and translate molecular findings into clinically applicable tools. By improving diagnostic accuracy, enabling prognostic stratification, and identifying novel therapeutic targets, the project addresses a critical unmet need in the management of cartilaginous tumours and lays the groundwork for future targeted and personalized treatment strategies.
- Conditions
- Chondrosarcomas, Cartilage Tumours
- Being tested
- Tumour tissue analysis, Molecular validation, Liquid biopsy analysis
- Keywords
- Chondrosarcoma, Liquid biopsy, Targeted therapy, Prognostic markers, Molecular biomarkers, MicroRNA (miRNA), Cartilaginous tumours, IDH1 mutation, IDH2 mutation
- Medical subject headings
- Chondrosarcoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Tumour tissue analysisDiagnostic test
Next-generation sequencing (NGS) to determine IDH1/2 mutation status
Global microRNA (miRNA) expression profiling using NGS
Molecular validationDiagnostic test
Quantitative reverse transcription PCR (RT-qPCR) to validate selected miRNAs
Targeted molecular assays for confirmation of IDH1/2 mutations
Liquid biopsy analysisDiagnostic test
Assessment of circulating and exosomal miRNAs from patient body fluids as non-invasive biomarkers
| Study group | Role | What they receive |
|---|---|---|
| Patients with cartilaginous bone tumours | The study cohort consists of patients with cartilaginous bone tumours treated at a tertiary orthopaedic oncology centre. This includes individuals with benign, borderline, and malignant chondroid lesions across the full biological spectrum, namely enchondromas, atypical cartilaginous tumours (ACT/G1), conventional chondrosarcomas (grades G1-G3), dedifferentiated chondrosarcomas, and selected rare variants. Interventions of interest in this study are primarily diagnostic and molecular, rather than therapeutic in the interventional trial sense.
Molecular analysis of tumour tissue using next-generation sequencing (NGS) to assess global microRNA expression profiles and IDH1/2 mutation status.
Validation of selected molecular markers using RT-qPCR and targeted mutation detection assays. Analysis of circulating and exosomal microRNAs from blood as a form of liquid biopsy. Experimental miRNA modulation to investigate biological relevance in relation to IDH1/2 mutation status. Receives: Diagnostic Test: Tumour tissue analysis; Diagnostic Test: Molecular validation; Diagnostic Test: Liquid biopsy analysis |
What is being measured
The primary outcome is the main question the study is designed to answer.
Diagnostic accuracy of molecular markers
Ability of IDH1/2 mutation status and tumour tissue miRNA expression profiles to: Distinguish benign cartilaginous tumours (enchondromas, atypical cartilaginous tumours) from malignant tumours (chondrosarcomas). Distinguish chondrosarcoma from chondroblastic osteosarcoma. Outcomes will be quantified using molecular classification performance (e.g. correct stratification against histopathological diagnosis) based on NGS and RT-qPCR analyses.
Measured: From May 2025 to December 2027
Identification of prognostic molecular signatures
Association between IDH1/2 mutation status and overall survival of patients with malignant cartilaginous tumours.
Identification of prognostic miRNA panels whose expression profiles stratify patients into different survival risk groups.
Measured: From May 2025 to December 2027
Secondary outcomes (2)
Validation of candidate biomarkers
Technical and biological validation of selected deregulated miRNAs and IDH1/2 mutations in an independent retrospective FFPE cohort using RT-qPCR and targeted mutation assays.
Reproducibility and stability of miRNA panels across different sample types (fresh-frozen vs FFPE tissue).
Measured: From May 2025 to December 2027
Liquid biopsy feasibility
Detection and quantification of circulating and exosomal miRNAs in prospectively collected body fluids.
Concordance between miRNA profiles in liquid biopsies and matched tumour tissue samples.
Measured: From May 2025 to December 2027
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Jan 2026
- Study start1 May 2025
- Primary completion31 Dec 2027 (estimated)
- Study completion31 Dec 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for ChondrosarcomasStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 300 participants (estimated)
- Target duration
- 5 Years
Sponsor and investigators
- Lead sponsor
- St. Anne's University Hospital Brno, Czech Republic
- Sponsor type
- University, hospital or other
- Collaborators
- Masaryk University
- Responsible party
- Sponsor
- Investigators
- Tomáš Tomáš, Assoc.Prof., M.D., Ph.D., Principal investigator, Faculty of Medicine, Masaryk University, Brno, 60200, CzechiaMichal Mahdal, M.D., Ph.D., Principal investigator, First Department of Orthopaedic Surgery, St. Anne's University Hospital, Brno, 60200, Czechia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07315542
- Sponsor's protocol ID
- NW25-10-00260
- Other IDs
- NW25-10-00260
- Status last verified
- Dec 2025
- First submitted
- 18 Dec 2025
- Last updated
- 5 Jan 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 5 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Finding New Diagnostic and Therapeutic Targets in Cartilaginous Tumours
- ClinicalTrials.gov ID
- NCT07315542
- Acronym / sponsor ID
- NW25-10-00260
- Conditions
- Chondrosarcomas, Cartilage Tumours
- Keywords
- Chondrosarcoma, Liquid biopsy, Targeted therapy, Prognostic markers, Molecular biomarkers, MicroRNA (miRNA), Cartilaginous tumours, IDH1 mutation
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 300 participants (estimated)
- Lead sponsor
- St. Anne's University Hospital Brno, Czech RepublicUniversity, hospital or other
- Collaborators
- Masaryk University
- Study start
- 1 May 2025 (actual)
- Primary completion
- 31 Dec 2027 (estimated)
- Study completion
- 31 Dec 2028 (estimated)
- First posted
- 2 Jan 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study, "Finding new diagnostic and therapeutic targets in cartilaginous tumours," focuses on improving the diagnosis, prognostic stratification, and treatment options for chondroid tumours, particularly chondrosarcoma. Chondrosarcoma is the most common primary malignant bone tumour in adults and is characterized by resistance to chemotherapy and radiotherapy, making accurate diagnosis and optimal surgical management critical. Distinguishing benign cartilage tumours (enchondromas, atypical cartilaginous tumours) from low-grade chondrosarcoma, and differentiating chondrosarcoma from chondroblastic osteosarcoma, remain major diagnostic challenges.
The project investigates two key molecular markers: mutations in IDH1/2 genes and non-coding microRNAs (miRNAs). IDH1/2 mutations are frequent in central chondrosarcomas and rare in other mesenchymal tumours, making them promising diagnostic markers. Their presence may also have prognostic significance and therapeutic relevance, as IDH inhibitors are already available for other malignancies. In parallel, deregulated miRNA expression has been implicated in chondrosarcoma biology, influencing tumour growth, invasion, angiogenesis, metastasis, and chemosensitivity. Preliminary data identified distinct miRNA signatures in chondrosarcoma compared with healthy cartilage, including previously unreported miRNAs.
The study is structured into exploratory and validation phases. Global miRNA expression profiling and IDH1/2 mutation analysis will be performed using next-generation sequencing (NGS) on prospectively collected fresh-frozen tumour samples. Selected miRNAs and IDH1/2 mutation status will then be validated by RT-qPCR and targeted mutation assays in a large retrospective cohort of FFPE samples. Molecular data will be integrated with clinicopathological parameters to develop diagnostic panels capable of accurately classifying chondroid tumours, as well as prognostic miRNA panels associated with patient survival.
Additionally, the project evaluates circulating and exosomal miRNAs in liquid biopsies, aiming to establish non-invasive diagnostic and prognostic tools. Functional relevance will be explored using chondrosarcoma cell lines with simulated miRNA upregulation, coupled with transcriptomic analysis.
Overall, the study seeks to refine diagnostic accuracy, improve prognostic assessment, and identify novel molecular targets for personalized and targeted therapy in patients with inoperable or metastatic chondrosarcoma, addressing a major unmet clinical need.
Detailed description
The study entitled "Finding new diagnostic and therapeutic targets in cartilaginous tumours" addresses major unresolved problems in the diagnosis, prognostic assessment, and treatment of chondroid tumours, with a particular focus on chondrosarcoma. Chondrosarcoma represents approximately 30% of all primary malignant bone tumours and is the most common malignant bone sarcoma in adults. Despite its clinical relevance, the management of chondrosarcoma remains challenging due to its biological heterogeneity, resistance to chemotherapy and radiotherapy, and frequent diagnostic uncertainty, especially in low-grade lesions.
A central clinical problem lies in the differentiation between benign cartilage tumours (enchondromas and atypical cartilaginous tumours), low-grade chondrosarcoma, higher-grade chondrosarcoma, and other malignant entities such as chondroblastic osteosarcoma. Histological assessment alone is often insufficient, particularly in small biopsy specimens, and diagnostic decisions frequently rely on a subjective combination of clinical, radiological, and pathological criteria. Incorrect classification may lead either to undertreatment with insufficient local control or overtreatment with unnecessarily radical surgery. Furthermore, advanced, inoperable, or metastatic chondrosarcoma has a very poor prognosis, and effective systemic therapies are currently lacking.
This project focuses on the identification and validation of molecular biomarkers that could significantly improve diagnostic precision, prognostic stratification, and therapeutic targeting. Two main molecular areas are investigated: IDH1/2 gene mutations and non-coding microRNAs (miRNAs).
Mutations in IDH1 and IDH2 genes have been identified as characteristic molecular events in cartilaginous tumours. These mutations occur at specific amino acid residues and lead to neomorphic enzymatic activity, resulting in the production of the oncometabolite 2-hydroxyglutarate. IDH1/2 mutations are common in central chondrosarcomas and related benign precursors but are rare or absent in peripheral chondrosarcomas and other mesenchymal tumours, including osteosarcoma. As such, IDH1/2 mutation status represents a highly valuable diagnostic marker, particularly for distinguishing chondrosarcoma from chondroblastic osteosarcoma, a distinction with major therapeutic implications. The study also hypothesizes that IDH1/2 mutations may be associated with tumour aggressiveness and poorer prognosis, making them potential prognostic markers and therapeutic targets. Importantly, IDH inhibitors already used in other malignancies may represent a future treatment option for selected chondrosarcoma patients.
The second major focus of the project is the role of microRNAs, short non-coding RNAs that regulate gene expression at the post-transcriptional level. Numerous studies have shown that miRNA dysregulation contributes to tumour initiation, progression, angiogenesis, invasion, and metastasis. In chondrosarcoma, specific miRNAs have been implicated in the regulation of key oncogenic pathways, including SRC, mTOR, Wnt/β-catenin signalling, VEGF-mediated angiogenesis, and matrix remodelling. Preliminary next-generation sequencing data generated by the research team identified distinct miRNA expression profiles in chondrosarcoma compared with healthy cartilage, including several miRNAs not previously reported in the literature. These findings support the existence of tumour-specific miRNA signatures with diagnostic and prognostic potential.
The study is designed in exploratory and validation phases. In the exploratory phase, prospectively collected fresh-frozen tumour samples will undergo global miRNA expression profiling using next-generation sequencing, alongside NGS-based analysis of IDH1/2 mutation status. This phase aims to identify characteristic molecular patterns across the spectrum of chondroid tumours, including benign lesions, low-grade and high-grade chondrosarcoma, dedifferentiated variants, and chondroblastic osteosarcoma.
In the validation phase, selected deregulated miRNAs and IDH1/2 mutations will be analysed in a large retrospective cohort of FFPE samples using RT-qPCR and targeted mutation detection methods. Molecular results will be integrated with detailed clinicopathological data to develop robust diagnostic miRNA panels capable of accurately classifying chondroid tumours and distinguishing chondrosarcoma from osteosarcoma. In parallel, prognostic miRNA panels will be established and correlated with overall survival using advanced statistical methods, including Kaplan-Meier analysis and Cox proportional hazards modelling.
An innovative component of the project is the evaluation of liquid biopsies, analysing circulating and exosomal miRNAs from patient body fluids. This approach aims to establish non-invasive biomarkers for diagnosis, prognosis, and disease monitoring beyond the time of surgery. Additionally, functional relevance will be explored using chondrosarcoma cell lines, in which selected miRNAs will be experimentally upregulated to assess downstream transcriptomic effects and their relationship to IDH1/2 mutation status.
Overall, this study aims to significantly advance the understanding of chondrosarcoma biology and translate molecular findings into clinically applicable tools. By improving diagnostic accuracy, enabling prognostic stratification, and identifying novel therapeutic targets, the project addresses a critical unmet need in the management of cartilaginous tumours and lays the groundwork for future targeted and personalized treatment strategies.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 5 Years
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients with cartilaginous bone tumours | – | Diagnostic Test: Tumour tissue analysis, Diagnostic Test: Molecular validation, Diagnostic Test: Liquid biopsy analysisThe study cohort consists of patients with cartilaginous bone tumours treated at a tertiary orthopaedic oncology centre. This includes individuals with benign, borderline, and malignant chondroid lesions across the full biological spectrum, namely enchondromas, atypical cartilaginous tumours (ACT/G1), conventional chondrosarcomas (grades G1-G3), dedifferentiated chondrosarcomas, and selected rare variants. Interventions of interest in this study are primarily diagnostic and molecular, rather than therapeutic in the interventional trial sense. Molecular analysis of tumour tissue using next-generation sequencing (NGS) to assess global microRNA expression profiles and IDH1/2 mutation status. Validation of selected molecular markers using RT-qPCR and targeted mutation detection assays. Analysis of circulating and exosomal microRNAs from blood as a form of liquid biopsy. Experimental miRNA modulation to investigate biological relevance in relation to IDH1/2 mutation status. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- The study population will consist of patients with cartilaginous (chondroid) tumours treated at the First Department of Orthopaedic Surgery, St. Anne's University Hospital Brno, a national referral centre for bone tumours.
Key inclusion criteria (8 listed)
- Histologically confirmed cartilaginous (chondroid) tumour
- Diagnosis includes one of the following entities (as available and eligible):
- Enchondroma
- Atypical cartilaginous tumour / Grade 1 chondrosarcoma (ACT/G1)
- Conventional chondrosarcoma (Grade 2-3)
Key exclusion criteria (1 listed)
- Insufficient, degraded, or otherwise unusable tissue samples
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Tumour tissue analysisNext-generation sequencing (NGS) to determine IDH1/2 mutation status Global microRNA (miRNA) expression profiling using NGS | Diagnostic test | Patients with cartilaginous bone tumours |
| Molecular validationQuantitative reverse transcription PCR (RT-qPCR) to validate selected miRNAs Targeted molecular assays for confirmation of IDH1/2 mutations | Diagnostic test | Patients with cartilaginous bone tumours |
| Liquid biopsy analysisAssessment of circulating and exosomal miRNAs from patient body fluids as non-invasive biomarkers | Diagnostic test | Patients with cartilaginous bone tumours |
Primary outcome
Diagnostic accuracy of molecular markers
Time frame: From May 2025 to December 2027
Ability of IDH1/2 mutation status and tumour tissue miRNA expression profiles to: Distinguish benign cartilaginous tumours (enchondromas, atypical cartilaginous tumours) from malignant tumours (chondrosarcomas). Distinguish chondrosarcoma from chondroblastic osteosarcoma. Outcomes will be quantified using molecular classification performance (e.g. correct stratification against histopathological diagnosis) based on NGS and RT-qPCR analyses.
Identification of prognostic molecular signatures
Time frame: From May 2025 to December 2027
Association between IDH1/2 mutation status and overall survival of patients with malignant cartilaginous tumours. Identification of prognostic miRNA panels whose expression profiles stratify patients into different survival risk groups.
2 secondary outcomes
Validation of candidate biomarkers
Time frame: From May 2025 to December 2027
Liquid biopsy feasibility
Time frame: From May 2025 to December 2027
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Jan 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Tomáš Tomáš, Assoc.Prof., M.D., Ph.D. principal investigator
Faculty of Medicine, Masaryk University, Brno, 60200, Czechia
Michal Mahdal, M.D., Ph.D. principal investigator
First Department of Orthopaedic Surgery, St. Anne's University Hospital, Brno, 60200, Czechia
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Chondrosarcomas and Cartilage Tumours, run by St. Anne's University Hospital Brno, Czech Republic at 1 site in Czechia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 8 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 5 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Czechia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Vasileios Apostolopoulos, M.D., Ph.D. (+420722101065, vasileios.apostolopoulos@fnusa.cz), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Diagnostic accuracy of molecular markers (time frame: From May 2025 to December 2027). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Jan 2026.