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Combining 3'-Deoxy-3'-[18F] fluorothymidine and MRI increases the sensitivity of glioma volume detection

Philippe Fernandez1,2,3, Paolo Zanotti-Fregonara4, Sandrine Eimer5,2

  • 1Service de Médecine Nucléaire.

Abstract

Insights

Combining 3'-Deoxy-3'-[18F] fluorothymidine (18F-FLT) PET scans with MRI detected more glioma tissue than MRI alone. However, 18F-FLT uptake did not predict tumor grade or prognosis.

Area of Science:

  • Neuro-oncology
  • Medical imaging
  • Nuclear medicine

Background:

  • 3'-Deoxy-3'-[18F] fluorothymidine (18F-FLT) is a positron emission tomography (PET) tracer used to assess cell proliferation.
  • 18F-FLT PET demonstrates a high tumor-to-background ratio in brain tumors.
  • Magnetic resonance imaging (MRI) is a standard modality for brain tumor evaluation.

Purpose of the Study:

  • To evaluate if combining 18F-FLT PET with MRI improves tumoral tissue detection compared to MRI alone.
  • To determine the prognostic value of 18F-FLT uptake by correlating it with histopathological features.

Main Methods:

  • Thirteen patients with supratentorial malignant glioma underwent 18F-FLT PET and MRI.
  • Tumor volumes were defined on both imaging modalities and coregistered onto a neuronavigation system.
  • Biopsies were taken from PET/MRI-positive and negative regions, and standardized uptake values (SUVs) were correlated with histopathology (proliferation index, mitoses).

Main Results:

  • Out of 149 biopsies, 109 contained tumoral tissue.
  • MRI alone had a positive predictive value of 93.1%, while MRI and 18F-FLT PET combined had 78.3%.
  • 40% of biopsies from PET/MRI-negative areas showed malignancy; SUV values did not correlate with proliferation index, mitoses, or tumor grade.

Conclusions:

  • Combining MRI and 18F-FLT PET detects additional tumoral tissue, potentially aiding surgical resection completeness.
  • The addition of negative PET to negative MRI enhances the negative predictive value.
  • 18F-FLT underestimated lesion margins and did not correlate with histopathological prognostic factors.

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