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. 2013 Dec;15(12):1347–1353. doi: 10.1593/neo.131666

Table 1.

[11C]-Erlotinib Tumor Imaging and Data Acquisition Parameters for Both High and Low SA Conditions.

Xenograft EGFR Properties SA n Voxels R1 BP SUV
SW620 WT* High 1 100 n/a 1 n/a -1 n/a 0.28 n/a
HCC827 Exon 19 del (E746-A750) 3 168 (13) 1.12 (0.22) 6.38 (1.90) 0.91 (0.60)
PC9 Exon 19 del (E746-A750) 3 82 (50) 0.787 (0.27) 2.45 (1.72) 0.45 (0.31)
U87 WT 3 102 (16) 1.3 (0.07) -0.69 (0.53) 0.51 (0.56)
U87Δ ΔEGFR 3 124 (23) 0.23 (0.08) -0.13 (0.20) 0.46 (0.29)
SW620 WT* Low 1 42 n/a 1.24 n/a -1 n/a 0.08 n/a
HCC827 Exon 19 del (E746-A750) 3 153 (57) 0.49 (0.35) 0.38 (0.27) 0.93 (1.33)
PC9 Exon 19 del (E746-A750) 3 72 (49) 0.53 (0.53) 0.12 (0.40) 0.48 (0.67)
U87 WT 2 100 (25) 1.75 (0.58) -0.43 (0.81) 0.33 (0.30)
U87Δ ΔEGFR 2 106 (62) 0.57 (0.27) 0.16 (0.79) 0.24 (0.16)

The mean number of voxels per ROI is reported along with SRTM calculated parameters and SUVs calculated at 90 minutes. Average R1 and BP values are used to quantify delivery of [11C]-erlotinib and receptor density, respectively. All values are shown as an average across sample size n with the SD in parentheses.

*

The WT EGFR of SW620 is not expressed at detectable levels.