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Clinical Trials/NCT07017790
NCT07017790CompletedNot Applicable

Amino Acid PET Imaging to Assess the Efficacy of IDH Inhibitor Treatments for Patients With Refractory IDH Mutated Gliomas

Central Hospital, Nancy, France1 site in 1 country22 target enrollmentStarted: June 30, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
22
Locations
1
Primary Endpoint
Compare the performance between amino acid PET and brain MRI to assess a treatment efficacy

Study Overview

Brief Summary

Amino acid PET imaging could represent a biomarker for the evaluation of IDH inhibitor treatments for patients with refractory IDH-mutated gliomas

Detailed Description

Amino acid PET imaging could represent a biomarker for the evaluation of IDH inhibitor treatments for patients with refractory IDH-mutated gliomas In fact, this study will allow us to assess, using Rano 1.0 criteria for PET and Rano 2.0 criteria for MRI, which of the two examinations is most effective in assessing the efficacy of anti-IDH treatment patients with refractory IDH-mutated gliomas.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients who underwent amino acid PET for early assessment of therapeutic response of IDH-mutated gliomas under anti-IDH treatment between February 2022 and November 2024

Exclusion Criteria

  • •Individuals who have objected to the use of their data

Outcomes

Primary Outcomes

Compare the performance between amino acid PET and brain MRI to assess a treatment efficacy

Time Frame: one day

Comparison between early therapeutic response according to RANO 1.0 and RANO 2.0 PET criteria and tumor progression at 6 months

Secondary Outcomes

  • Compare the performance between amino acid PET and brain MRI to assess a treatment efficacy for the identification of lesions(one day)

Investigators

Sponsor
Central Hospital, Nancy, France
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Antoine VERGER

Principal investigator

Central Hospital, Nancy, France

Study Sites (1)

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