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| Name | Class |
|---|---|
| Maastricht University Medical Center | OTHER |
| Zuyderland Medisch Centrum | OTHER |
| Ziekenhuis Oost-Limburg | OTHER |
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There is a high medical need to improve treatment outcome for high-grade and low-grade glioma since no curative treatment is available. To achieve this goal, a broader understanding is needed of the causes of inter-and intratumoral heterogeneity; glioma dedifferentiation and invasion; the major determinants of malignancy and treatment failure in glioma patients. Patient-derived organoid (PDOs) of high-grade gliomas and low-grade gliomas will be used to identify the mechanisms that underlie this malignant behaviour and treatment resistance. This insight may be used to develop patient avatars to simultaneously test multiple new treatment modalities that are predictive for survival and quality of life of glioma patients.
To establish primary patient-derived three-dimensional organoid cultures from low grade and high-grade gliomas to study the mechanisms that contribute to i.e.
resistance to radiotherapy and/or chemotherapy and immunotherapy, dedifferentiation, tumor invasion among others, in primary and recurrent tumors.
Primary Objectives:
Secondary objectives
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Low grade glioma patients | Patients who have a MRI lesion suspected for a low grade glioma (newly diagnosed or recurrent), who are eligible for a resection of the tumor | ||
| High grade glioma patients | Patients who have a MRI lesion suspected for a high grade glioma (newly diagnosed or recurrent), who are eligible for a resection of the tumor |
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| Measure | Description | Time Frame |
|---|---|---|
| Phenotypic, genetic, epigenetic proteomic and transcriptomic profile of the LGG/HGG PDOs | Phenotypic, genetic, epigenetic proteomic and transcriptomic profile of the LGG/HGG PDOs will be performed after establishing PDO and the data will be compared with the phenotypic, genetic, epigenetic, proteomic and transcriptomic profile of the parental tumor. DNA isolated from peripheral blood will be used as normal reference DNA for (epi)genetic profiling. | Baseline tumor resection and blood sampling |
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Inclusion Criteria:
Exclusion Criteria:
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Patients who have an MRI lesion suspected for a low- or high grade glioma (newly diagnosed or recurrent), who are eligible for a resection of the tumor.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Annika Noordink, Msc | Contact | +31(0)884456010 | annika.noordink@maastro.nl | |
| Chantal Overhof | Contact | +31(0)884455686 | chantal.overhof@maastro.nl |
| Name | Affiliation | Role |
|---|---|---|
| Marc Vooijs, Prof. Dr. | Maastro Radiaton Oncology clinic | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Maastricht Radiation Oncology | Recruiting | Maastricht | Limburg | 6229ET | Netherlands |
All obtained research data points and information will be added in a coded manner to the existing database of Laboratory Radiotherapy, located on a MUMC+ hosted and secured server and is password protected. A dedicated, trained person will add all genetic and research information from this project to the database, which was especially designed for this research. Only coded information will be extracted and used for the downstream research analyses.
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| ID | Term |
|---|---|
| D005910 | Glioma |
| ID | Term |
|---|---|
| D018302 | Neoplasms, Neuroepithelial |
| D017599 | Neuroectodermal Tumors |
| D009373 | Neoplasms, Germ Cell and Embryonal |
| D009370 | Neoplasms by Histologic Type |
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Tumor tissue, blood
| D009369 | Neoplasms |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009380 | Neoplasms, Nerve Tissue |