Clinical Trial Matcher

NCT05274919

Vascular Signature Mapping of Brain Tumor Genotypes

Recruiting · Not specified · Leiden University Medical Center · registry updated 2025-03-10

Inclusion and exclusion lines below are quoted from ClinicalTrials.gov. No match score is shown, because a score needs a person's age, biomarkers, and treatment dates. Confirm the record with the study team.

A glioma is a primary brain tumor in adults that is characterized by a highly variable, but overall poor survival. The optimal timing of treatment is in part determined by the expected biological behavior of the tumor. At present the expected biological behavior, determined by the tumor genotype, can only be determined by tissue analysis, which requires brain surgery. Non-invasive and improved diagnostic methods are sought to obtain insight into the molecular profile of the tumor and the expected biological behavior to avoid surgery performed solely for diagnostic purposes. Vascularization is an important aspect of the biological behavior of a primary brain tumor. Tumor vascularization characteristics can be assessed by Magnetic Resonance Imaging (MRI), but with the currently available technology this can only be achieved with unacceptably long scan times. In this proposal, the investigators will develop and optimize a novel MRI protocol to gather a large set of quantitative vascularization parameters within an acceptable scan time. The hypothesis is that from such a 'vascular signature' the tumor genotype can be inferred by means of machine learning.

Inclusion

  • Patients scheduled for brain MRI with contrast injection as part of the clinical diagnostic procedure (cohort 1)
  • Patients diagnosed with suspected glioma scheduled for brain MRI as part of the clinical diagnostic procedure (cohort 2)
  • Patients with (suspected) glioma referred for tumor biopsy or resection (cohort 3)
  • Age ≥ 18 years (all cohorts)
  • Signed informed consent (all cohorts)

Exclusion

  • Subjects with contra-indications for an MRI exam
  • Subjects with reduced kidney function because of the risk on developing nephrogenic systemic fibrosis (NSF) under gadolinium-based contrast injection
  • Subjects with pregnancy
  • Subjects undergoing a clinical protocol that requires scanning during CA injection (cohort 1)

Open NCT05274919 on ClinicalTrials.govAll conditions