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First published online May 15, 2007, 10.2967/jnumed.106.037382
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Dynamic and Static Approaches to Quantifying 18F-FDG Uptake for Measuring Cancer Response to Therapy, Including the Effect of Granulocyte CSF

Robert K. Doot1,2, Lisa K. Dunnwald2, Erin K. Schubert2, Mark Muzi2, Lanell M. Peterson2, Paul E. Kinahan1,2, Brenda F. Kurland3 and David A. Mankoff1,2

1 Department of Bioengineering, University of Washington, Seattle, Washington; 2 Division of Nuclear Medicine, University of Washington, Seattle, Washington; and 3 Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington


Figure 1
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FIGURE 1.  Coronal and sagittal 18F-FDG PET images of same patient before treatment (A) and after neoadjuvant chemotherapy including granulocyte CSF (B). Right breast cancer decreased in 18F-FDG activity after treatment (arrowheads), whereas 18F-FDG activity increased in marrow in spine, sternum, and ribs (open arrows).

 

Figure 2
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FIGURE 2.  Mean 18F-FDG blood clearance time–activity curves for patients (n = 39) before treatment and after chemotherapy including granulocyte CSF, with close-up of last 4 time bins with SE bars on middle time points (inset). Area under curve significantly decreased after treatment (P = 0.02).

 

Figure 3
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FIGURE 3.  SUV vs. MRFDG for all patients before treatment (+ and dashed line) and after granulocyte CSF–containing chemotherapy regimes ({circ} and solid line).

 

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FIGURE 4.  Percentage change in SUV vs. percentage change in MRFDG for all (n = 39) patients (A), first patient tertile ({circ}, n = 13) with lowest baseline SUVs (B), and second and third patient tertiles (+, n = 26) with higher baseline SUVs (C). Maximum detectable percentage change in SUV (*) is mean percentage alteration in tumor metabolism that can be detected using SUV algorithm assuming that MRFDG model can detect 100% decrease in tumor metabolic activity.

 





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