Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07121842

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

Led by Erasmus Medical Center · Updated on 2025-08-14

120

Participants Needed

4

Research Sites

128 weeks

Total Duration

On this page

Sponsors

E

Erasmus Medical Center

Lead Sponsor

U

UMC Utrecht

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of glioblastoma by biopsy or suspected 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
Not Eligible

You will not qualify if you...

  • Unable to give informed consent
  • Contraindication for MRI
  • Brain conditions affecting CEST contrast, such as recent stroke or previous cranial radiotherapy as determined by investigators

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Amsterdam UMC

Amsterdam, Netherlands

Not Yet Recruiting

2

Leiden UMC

Leiden, Netherlands

Actively Recruiting

3

Erasmus MC

Rotterdam, Netherlands

Actively Recruiting

4

UMC Utrecht

Utrecht, Netherlands

Actively Recruiting

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Research Team

L

Laura Kemper, MSc

CONTACT

E

Esther Warnert, PhD, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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