Assessment of the effect of therapy in a rat model of glioblastoma using [18F]FDG and [18F]FCho PET compared to contrast-enhanced MRI

PLoS One. 2021 Mar 5;16(3):e0248193. doi: 10.1371/journal.pone.0248193. eCollection 2021.

Abstract

Objective: We investigated the potential of [18F]fluorodeoxyglucose ([18F]FDG) and [18F]Fluoromethylcholine ([18F]FCho) PET, compared to contrast-enhanced MRI, for the early detection of treatment response in F98 glioblastoma (GB) rats.

Methods: When GB was confirmed on T2- and contrast-enhanced T1-weighted MRI, animals were randomized into a treatment group (n = 5) receiving MRI-guided 3D conformal arc micro-irradiation (20 Gy) with concomitant temozolomide, and a sham group (n = 5). Effect of treatment was evaluated by MRI and [18F]FDG PET on day 2, 5, 9 and 12 post-treatment and [18F]FCho PET on day 1, 6, 8 and 13 post-treatment. The metabolic tumor volume (MTV) was calculated using a semi-automatic thresholding method and the average tracer uptake within the MTV was converted to a standard uptake value (SUV).

Results: To detect treatment response, we found that for [18F]FDG PET (SUVmean x MTV) is superior to MTV only. Using (SUVmean x MTV), [18F]FDG PET detects treatment effect starting as soon as day 5 post-therapy, comparable to contrast-enhanced MRI. Importantly, [18F]FDG PET at delayed time intervals (240 min p.i.) was able to detect the treatment effect earlier, starting at day 2 post-irradiation. No significant differences were found at any time point for both the MTV and (SUVmean x MTV) of [18F]FCho PET.

Conclusions: Both MRI and particularly delayed [18F]FDG PET were able to detect early treatment responses in GB rats, whereas, in this study this was not possible using [18F]FCho PET. Further comparative studies should corroborate these results and should also include (different) amino acid PET tracers.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Choline / analogs & derivatives*
  • Choline / pharmacology
  • Contrast Media / pharmacology*
  • Female
  • Fluorodeoxyglucose F18 / pharmacology*
  • Glioblastoma* / diagnostic imaging
  • Glioblastoma* / therapy
  • Magnetic Resonance Imaging*
  • Neoplasms, Experimental* / diagnostic imaging
  • Neoplasms, Experimental* / therapy
  • Positron-Emission Tomography*
  • Rats
  • Rats, Inbred F344

Substances

  • Contrast Media
  • fluoromethylcholine
  • Fluorodeoxyglucose F18
  • Choline

Grants and funding

Lux Luka Foundation supported this study financially. Funds were received by Prof. I. Goethals and Prof. T. Boterberg. The sponsor did not play a role in study design and analysis.