Actively Recruiting
Amino Acid PET-based Response Assessment in IDH-mutant Gliomas (APPEAR)
Led by LMU Klinikum · Updated on 2025-09-08
100
Participants Needed
2
Research Sites
260 weeks
Total Duration
On this page
Sponsors
L
LMU Klinikum
Lead Sponsor
S
Servier Affaires Médicales
Collaborating Sponsor
AI-Summary
What this Trial Is About
Background: The radiological follow-up of diffuse gliomas is challenged by the difficult distinction of true progression from treatment-related changes. To this end, the Response Assessment in Neuro-Oncology (RANO) Working Group has issued specific recommendation for the standardized evaluation of magnetic resonance imaging (MRI). In addition, positron emission tomography (PET) using radiolabeled amino acids allows for the delineation of metabolically active tumor regions in brain tumors, and guidelines for PET-based response assessment have been recently proposed (PET RANO 1.0). However, well-annotated data on longitudinal PET alterations before and during treatment and follow-up are missing in isocitrate dehydrogenase (IDH)-mutant gliomas, particularly as tumor entities defined by IDH mutations have been established only recently and data on PET imaging mainly rely on previous brain tumor classification frameworks. 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.
CONDITIONS
Official Title
Amino Acid PET-based Response Assessment in IDH-mutant Gliomas (APPEAR)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Histologically confirmed diffuse IDH-mutant glioma (astrocytoma or oligodendroglioma) of any grade
- Receiving postoperative treatment according to current standard of care at study entry
- Undergoing amino acid PET imaging as part of clinical routine
You will not qualify if you...
- Participation in another clinical trial involving experimental therapy or study medication
- Not meeting the inclusion criteria
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Medical University of Vienna
Vienna, Austria, 1090
Actively Recruiting
2
LMU Hospital
Munich, Bavaria, Germany, 81377
Actively Recruiting
Research Team
N
Nathalie L Albert, Prof. Dr. med
CONTACT
M
Matthias Preusser, Prof. Dr. med.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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