CD138+-plasma cells were incubated with either 18F-FDG, 18F-FET or 11C-MET for 60 min and intracellular radioactivity was quantified using a gamma-counter. Relative uptake of background- and decay-corrected samples was expressed as cpm per 1000 cells. Whenever possible, bone marrow samples were split and one half of the sample was incubated with 18F-FDG, the other with either 18F-FET (patients no 7, 10, 11) or 11C-MET (patients no. 13, 16, 17, 18, 19, 21, 22, 26). (A) 18F-FDG, 18F-FET and 11C-MET uptake by CD138+ PCs. Data from all samples analyzed are shown. (B) Direct comparison of 18F-FDG and 11C-MET uptake in split samples. Lines indicate corresponding samples from one patient.