Amino Acid PET-based Response Assessment in IDH-mutant Gliomas (APPEAR)
NCT ID: NCT07159607
Last Updated: 2025-09-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
100 participants
OBSERVATIONAL
2025-07-17
2030-07-16
Brief Summary
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Aims: This bicentric, prospective, observational study aims to collect data on imaging-based disease monitoring in patients with IDH-mutant gliomas. Specifically, this study aims to investigate longitudinal changes of amino acid PET tracer uptake during treatment in IDH-mutant gliomas and to evaluate the correlation between amino acid PET uptake at baseline and response to postoperative standard of care treatment.
Patient cohort/methods: Adult (age ≥ 18 years) patients diagnosed and/or treated at the Medical University of Vienna (Vienna, Austria) or the LMU Hospital Munich (Munich, Germany) with histologically verified diffuse IDH-mutant glioma (oligodendroglioma, astrocytoma of all grades) and PET imaging for routine follow-up before, during and after treatment will be included. Clinical and imaging data will be collected in a standardized manner and correlated with treatment response. Primary endpoint is progression-free survival (PFS) according to RANO 2.0 criteria, secondary endpoints include PFS according to PET-RANO 1.0 criteria, time to next intervention (TTNI) and overall survival (OS).
Originality/relevance: This study will generate data that will inform future response assessment frameworks and the design of future clinical trials in IDH-mutant glioma.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Histologically verified diffuse IDH-mutant glioma (astrocytoma, oligodendroglioma) of any grade as defined in the WHO classification of tumors of the central nervous system
* Postoperative treatment according to current standard of care at the time of study inclusion
* Performance of amino acid PET as part of clinical routine
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Servier Affaires Médicales
INDUSTRY
Servier Deutschland GmbH
INDUSTRY
LMU Klinikum
OTHER
Responsible Party
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Nathalie Albert
Prof. Dr. med.
Principal Investigators
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Nathalie L Albert, Prof. Dr. med.
Role: PRINCIPAL_INVESTIGATOR
LMU Klinikum München
Locations
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Medical University of Vienna
Vienna, , Austria
LMU Hospital
Munich, Bavaria, Germany
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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24-1114
Identifier Type: -
Identifier Source: org_study_id
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