Reproducibility of Static and Dynamic 18F-FDG, 18F-FLT, and 18F-FMISO MicroPET Studies in a Murine Model of HER2+ Breast Cancer |
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Authors: | Jennifer G. Whisenant Todd E. Peterson Jacob U. Fluckiger Mohammed Noor Tantawy Gregory D. Ayers Thomas E. Yankeelov |
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Affiliation: | 1. Institute of Imaging Science, Vanderbilt University Medical Center, 1161 21st Ave. South, MCN AA-1105, Nashville, TN, 37232-2675, USA 6. Department of Cancer Biology, Vanderbilt University, Nashville, TN, 37232-2675, USA 2. Department of Radiology and Radiological Sciences, Vanderbilt University, Nashville, TN, 37232-2675, USA 4. Department of Physics and Astronomy, Vanderbilt University, Nashville, TN, 37232-2675, USA 3. Department of Radiology, Northwestern University, 676 N Saint Clair, Chicago, IL, 60611, USA 5. Department of Biostatistics, Vanderbilt University, Nashville, TN, 37232-2675, USA
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Abstract: | Purpose The objective of this study is to determine the reproducibility of static 2-deoxy-2-[18F]fluoro-D-glucose (18F-FDG), 3′-deoxy-3′-[18F]fluorothymidine (18F-FLT), and [18F]-fluoromisonidazole (18F-FMISO) microPET measurements, as well as kinetic parameters returned from analyses of dynamic 18F-FLT and 18F-FMISO data. Procedures HER2+ xenografts were established in nude mice. Dynamic data were acquired for 60 min, followed by a repeat injection and second scan 6 h later. Reproducibility was assessed for the percent-injected dose per gram (%ID/g) for each radiotracer, and with kinetic parameters (K 1 –k 4 , K i ) for 18F-FLT and 18F-FMISO. Results The value needed to reflect a change in tumor physiology is given by the 95 % confidence interval (CI), which is ±14, ±5, and ±6 % for 18F-FDG (n?=?12), 18F-FLT (n?=?11), and 18F-FMISO (n?=?11) %ID/g, respectively. V d (=K 1 /k 2), k 3, and K FLT are the most reproducible 18F-FLT (n?=?9) kinetic parameters, with 95 % CIs of ±18, ±10, and ±18 %, respectively. V d and K FMISO are the most reproducible 18F-FMISO kinetic parameters (n?=?7) with 95 % CIs of ±16 and ±14 %, respectively. Conclusions Percent-injected dose per gram measurements are reproducible and appropriate for detecting treatment-induced changes. Kinetic parameters have larger threshold values, but are potentially sufficiently reproducible to detect treatment response. |
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