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Clinical Trials in the Netherlands / NCT07121842
Recruiting Not applicable

Glioblastoma Imaging for the Detection of Tumor Progression Using APTw-CEST MRI

NCT07121842 · tracked via the Priya Life Science Netherlands tracker
Phase
Not applicable
Started
2025-01-15
Last updated
2025-08-14

Condition(s) studied

Glioblastoma

Investigational drug(s) / intervention(s)

Extended MRI

Extended MRI: The MRI protocol for every clinical follow-up MRI scan is extended with 15 minutes to add the APTw-CEST scan.

Study summary

In this study, the invesigators look at how a new MRI technique (called amide proton transfer weighted (APTw) chemical exchange saturation transfer (CEST)) can improve treatment for brain tumors through early detection of tumor progression after radiotherapy and/or chemotherapy treatment.

An issue with the current treatment for patients with a brain tumor, is the inability to detect tumor progression early. An abnormality is seen on MRI scans taken shortly after treatment with radiotherapy in about 30% of patients.

This abnormality may be a sign that radiotherapy treatment has worked well and will disappear on its own after a while. However, an abnormality can also be a sign of active tumor tissue. Then it shows that the treatment has not worked well enough. When there is active tumor tissue, this is called 'tumor progression'. When there is an abnormality that disappears on its own after a while, there is no active tumor tissue. This is called 'pseudoprogression'.

Currently, there are two options to determine whether tumor progression or pseudoprogression has taken place: Do another brain surgery to see if the abnormality contains active tumor tissue or wait and have regular MRI scans until it is clear whether the abnormality goes away on its own.

Amide proton transfer weighted chemical exchange saturation transfer (APTw-CEST) imaging is a new MRI technique in which investigators can produce images that show the accumulation of protein. APTw-CEST has previously been shown to be able to distinguish tumor progression from pseudoprogression earlier than current standard MRI scans. However, these previous studies have drawbacks: they were either done with a small group of patients in 1 hospital, or with a 7 Tesla MRI scanner, a rare type of scanner not standard in hospitals, or done in animal models.

In this research project the investigators now want to prepare APTw-CEST for standard patient care for patients with glioblastoma in the Netherlands so that in the future APTw-CEST can be included as a standard scan during treatment. The investigators are doing this by introducing APTw-CEST MRI on the clinical MRI scanners of four different hospitals. Ultimately, the investigators want to use this to create national guidelines for measuring and viewing APTw-CEST MRI images for early detection of tumor progression.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Confirmed diagnosis of glioblastoma based on histopathological or molecular analysis of biopsy after surgery, or suspected of glioblastoma based on medical imaging. * Scheduled to undergo radiotherapy or combined chemo-and radiotherapy * 18 years and older * Able to give informed consent. * Patient will undergo clinically indicated MRIs Exclusion Criteria: * Not able to give informed consent * Contraindication for MRI * Brain pathology affecting CEST contrast, such as recent stroke or earlier cranial radiotherapy, as determined by the principal investigators (PIs)

Primary outcome measure(s)

Trial sites (4)

FacilityCityRegionStatus
Amsterdam UMC Amsterdam Netherlands Not Yet Recruiting
Leiden UMC Leiden Netherlands Recruiting
Erasmus MC Rotterdam Netherlands Recruiting
UMC Utrecht Utrecht Netherlands Recruiting

More Erasmus Medical Center trials in the Netherlands

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07121842 on ClinicalTrials.gov ↗ ← All trials in the Netherlands