Construction and Application of an IDH Mutation-Targeted PET/MRI Imaging Framework for Precision Diagnosis of Gliomas

ConditionGlioma
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorDaping Hospital and the Research Institute of Surgery of the Third Military Medical University

About this trial

Glioma is the most common primary intracranial tumor in adults, with high-grade gliomas accounting for more than 50% of all gliomas and having the highest mortality rate. The molecular characteristics of gliomas are closely associated with the selection of treatment regimens, therapeutic efficacy, and patient prognosis. Mutations in isocitrate dehydrogenase (IDH) are an important diagnostic marker for diffuse gliomas and a key component in distinguishing and defining glioma subtypes. Furthermore, the advent of IDH-targeting inhibitors has brought hope to patients with IDH-mutant gliomas. Therefore, accurately assessing the IDH mutation status of gliomas is a prerequisite and key to precision diagnosis, targeted therapy, and prognostic evaluation. This study explores the application value of targeted IDH PET/MRI imaging in glioma subtype diagnosis, tumor grading, and prognostic evaluation. It aims to establish a non-invasive in vivo tracing technology platform and evaluation system for accurately assessing glioma IDH mutation status, subtype diagnosis, and prognostic evaluation. This will provide a basis for the precise diagnosis of gliomas, the selection of targeted treatment regimens, and prognostic assessment, and promote future research and development of therapeutic drugs using labeled therapeutic radionuclides.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient ≥ 18 years of age at the time of consent;

Patients with suspected, newly diagnosed, or previously treated gliomas;

Provided written informed consent authorisation before participating in the study.

Disqualifiers

Pregnancy or lactation;

MRI contraindications, not limited to cardiac implantable electronic devices and claustrophobia;

Participants with radiation exposure exceeding 50 mSv in the past year.

Trial population

The subjects the investigators selected are adults who are not restricted by gender.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • Targeted IDH PET/MRI

    Diagnostic test

    Patients with clinical suspected gliomas will receive the targeted IDH PET/MRI.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Diagnostic efficacy, survival analysis

sensitivity, specificity, accuracy, positive and negative predictive values, ROC curve analysis,

Time frame
Completed within half year after end of the study

Secondary outcomes

Other outcomes

Sponsors and contacts

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