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. 2017 Apr 5;7(6):1489–1498. doi: 10.7150/thno.18754

Table 3.

Heterogeneity of NET biology, as indicated by PET. In G1 NET, the vast majority of lesions showed sole expression of SSTR2, as indicated by focal retention of [68Ga]DOTATOC (104 lesions), and only few (11 lesions) concurrent glucose use, as indicated by [18F]FDG-PET. No lesion was positive at [68Ga]Pentixafor PET indicating no CXCR4 expression. In G3 NET, the vast majority of lesions revealed various combinations of SSTR and CXCR4 expression with or without deregulated glucose use.

G1 NET [68Ga]DOTATOC [18F]FDG [68Ga]Pentixafor
[68Ga]DOTATOC 104 11 0
[18F]FDG - 0 0
[68Ga]Pentixafor - - 0
G2 NET [68Ga]DOTATOC [18F]FDG [68Ga]Pentixafor
[68Ga]DOTATOC 107 10 3
[18F]FDG - 3 3
[68Ga]Pentixafor - - 0
G3 NET [68Ga]DOTATOC [18F]FDG [68Ga]Pentixafor
[68Ga]DOTATOC 0 11 12
[18F]FDG - 47 56
[68Ga]Pentixafor - - 9

Since some lesions were positive for all three tracers, the sum of lesions can exceed the number given in the manuscript. [68Ga]DOTATOC = 68Ga-DOTA-D-Phe-Tyr3-octreotide, [18F]FDG = 18F-fluorodeoxy-glucose.