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FET-PET for Diagnosis and Monitoring in Patients With Low Grade Glioma

Molecular Correlates and Clinical Significance of Positron Emission Tomography With FET-PET in Combination With Perfusion-weighted Magnetic Resonance Imaging (PWI) in Patients With Low Grade Gliomas

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01089244
Enrollment
38
Registered
2010-03-18
Start date
2008-06-30
Completion date
2015-12-31
Last updated
2015-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Astrocytoma, Oligoastrocytoma, Oligodendroglioma

Keywords

Low grade glioma, Astrocytoma, Molecular imaging, FET PET, Therapy monitoring, Temodar

Brief summary

The aim of the study is to compare the two imaging modalities perfusion weighted MR-imaging and FET-PET in their ability to provide an accurate histological evaluation of low grade glioma and to reveal focal abnormalities within a homogeneously appearing tumor. Additionally, therapeutic effects should be assessed during a time period of two years.

Interventions

None listed

Sponsors

Deutsche Krebshilfe e.V., Bonn (Germany)
CollaboratorOTHER
Ludwig-Maximilians - University of Munich
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* neuroradiologically suspected low grade glioma (Astrocytoma WHOI-II, Oligodendroglioma WHO II, Oligoastrocytoma WHO II) * histological verification will be obtained either by microsurgery or by stereotactic biopsy * patients older than 18 years * Karnofsky Performance Score \>=70 * pregnant or nursing female patients will not be included in this study

Exclusion criteria

* patients in whom informed consent cannot be obtained due to organic brain syndrome or insufficient language skills * patients who cannot lie quiet for a time period of app. two hours during the FET-PEt scan * medical history of a metastatic brain disease * patients in whom an MRI scan cannot be performed due to claustrophobia metallic protheses or pacemakers etc.

Design outcomes

Primary

MeasureTime frame
Overall survival24 months

Secondary

MeasureTime frame
Progression Free survival24 months

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026