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SUV Varies with Time After Injection in 18F-FDG PET of Breast Cancer: Characterization and Method to Adjust for Time Differences

Sylvain Beaulieu, MD, Paul Kinahan, PhD, Jeffrey Tseng, MD, Lisa K. Dunnwald, BS, Erin K. Schubert, BS, Pam Pham, BS, Barbara Lewellen, BS and David A. Mankoff, MD, PhD

Division of Nuclear Medicine, University of Washington Medical Center, Seattle, Washington



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FIGURE 1. Tumor time–activity curves of VOIs for all patients: Sav (A) and Smax (B) vs. time.

 


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FIGURE 2. Example of linear fit for 2 lesions, one for which linear regression generated positive slope (A) and another for which linear regression generated negative slope (B).

 


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FIGURE 3. Rate of average Sav change vs. measured Sav at 57 min. SUV measurements were not corrected for plasma glucose concentrations.

 


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FIGURE 4. Rate of SUV change vs. SUV at single time point for different single uptake time points: glucose-corrected Sav (A) and glucose-corrected SUVmax (B). These plots can be used to compare SUV measured at different times between studies.

 


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FIGURE 5. Illustration of proposed SUV correction method where SUV increases linearly with time, and rate of change (dS/dt) at any fixed time increases linearly with SUV value (S) at that time (dashed lines). From any measured point, a desired point can be extrapolated by use of a predetermined reference point as given in Equations 3 and 5 and Table 1.

 


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FIGURE 6. Estimated Smax at 71–75 min after injection (using Eq. 3) compared with measured value at 71–75 min for 20 additional locally advanced breast cancer lesions in patients not included in original analysis.

 





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