RT Journal Article
SR Electronic
T1 Evaluation of d-18F-FMT, 18F-FDG, l-11C-MET, and 18F-FLT for Monitoring the Response of Tumors to Radiotherapy in Mice
JF Journal of Nuclear Medicine
JO J Nucl Med
FD Society of Nuclear Medicine
SP 290
OP 295
DO 10.2967/jnumed.108.057091
VO 50
IS 2
A1 Murayama, Chieko
A1 Harada, Norihiro
A1 Kakiuchi, Takeharu
A1 Fukumoto, Dai
A1 Kamijo, Akemi
A1 Kawaguchi, Akira T.
A1 Tsukada, Hideo
YR 2009
UL http://jnm.snmjournals.org/content/50/2/290.abstract
AB O-18F-fluoromethyl-d-tyrosine (d-18F-FMT) is a promising novel agent for tumor imaging by PET. The aim of this study was to evaluate the potential of d-18F-FMT and the other conventional ligands used for tumor imaging, namely, 18F-FDG, l-11C-methionine (l-11C-MET), and 3′-deoxy-3′-18F-fluorothymidine (18F-FLT), as a PET ligand for monitoring early responses to radiotherapy in tumor-bearing mice. Methods: C3H/HeN mice inoculated with murine squamous cell carcinomas were treated with a single dose of x-ray irradiation at 2, 6, 20, or 60 Gy. Tumor uptake of each ligand was examined 1, 3, and 7 d after the irradiation. Results: Tumor uptake of d-18F-FMT was decreased on day 1 after irradiation at 6, 20, or 60 Gy, and the decrease persisted until day 7. Tumor uptake of 18F-FDG was elevated on days 1 and 3 after irradiation at 2, 6, or 20 Gy, followed by a decrease in uptake on day 7 in mice irradiated at 20 or 60 Gy. Decreased tumor uptake of l-11C-MET was observed only on day 3 after the irradiation. Decreased tumor uptake of 18F-FLT was detected on day 1 after irradiation at 2, 6, 20, or 60 Gy; thereafter, the dose-dependent decrease in uptake was no longer seen. Only for d-18F-FMT were significant positive correlations found between ligand uptake at all the time points examined and tumor volume on day 14 after various doses of irradiation. Conclusion: The findings suggest that d-18F-FMT is a promising PET ligand for early-phase detection and prediction of the effects of radiation therapy.