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. 2016 Nov 17;1(19):e90064. doi: 10.1172/jci.insight.90064

Figure 5. Quantitative PET for detection of CAR T cells and luminescence of tumor burden in survivors vs. nonsurvivors.

Figure 5

Representative longitudinal, PET/CT (coronal view of 20-mm-thick plane, maximum intensity projection [MIP]) and concurrent bioluminescence imaging of survivors (n = 4) (A) vs. nonsurvivors (n = 5) (E). Diaphragms are traced with dotted lines, drawn to visualize tumor burdens separately in lungs and liver. Trend-line graphs plot region of interest (ROI) values for DOTATOC uptake (percentage injection dose per volume [%ID/cm3]) against bioluminescence values (photons [P]/sec) in the lungs taken from the same mice on the same day. Luminescence images are drawn with the same upper bound (106 P/mm2/sec) with gradually increasing lower bounds (X16, X20 for 2.5 × 104 P/mm2/sec and X23, X27 for 5 × 104 P/mm2/sec) for clarity of delineating tumor burden. Longitudinal PET/CT images of the upper body cropped at the kidney apex are drawn with a uniform range of DOTATOC concentrations (0.5–5.0 %ID/cm3), while whole-body PET/CT images are drawn in 0.5–5.0 %ID/cm3 for (A) and 1–10 %ID/cm3 for (E). Quantification of luminescence and DOTATOC uptake by the lungs (B and F) and body weight change (C and G) is shown for survivors and nonsurvivors. Representative longitudinal, PET/CT (transverse view of 1-mm-thick plane, MIP) views of lungs are shown for survivors (D) and nonsurvivors (H). PET images are drawn in indicated ranges. X, number of days after tumor xenograft; SR, treated with SSTR2-R6.5-CAR–transduced T cells.