<sup>68</sup>Ga-fibroblast activation protein inhibitor PET/CT on gross tumour volume delineation for radiotherapy planning of oesophageal cancer.

Zhao, Liang; Chen, Shanyu; Chen, Sijia; Pang, Yizhen; Dai, Yaqing; Hu, Shenping; Lin, Li'e; Fu, Lirong et al. · Radiother Oncol · 2021

prospective_cohort · Level II

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Abstract

To compare <sup>68</sup>Ga-fibroblast activation protein inhibitor (FAPI) and <sup>18</sup>F-FDG PET/CT in imaging locally advanced oesophageal cancer, and evaluate the potential usefulness of <sup>68</sup>Ga-FAPI PET/CT on gross target volume (GTV) delineation aimed at radiotherapy planning for oesophageal cancer as compared with contrast-enhanced CT (CE-CT) and <sup>18</sup>F-FDG PET/CT. Twenty-one patients with newly diagnosed oesophageal cancer who underwent both <sup>18</sup>F-FDG and <sup>68</sup>Ga-FAPI PET/CT scans were selected. GTVs of the primary tumours based on CE-CT (GTV<sub>CT</sub>), PET/CT, and CE-CT plus PET/CT were delineated. Gross tumour lengths were measured by GTVs and endoscopy and recorded. The <sup>68</sup>Ga-FAPI PET showed significantly higher radiotracer uptake than <sup>18</sup>F-FDG PET (median SUVmax 16.71 vs. 11.23; P = 0.002) in the primary tumours. SUV thresholds of FAPI ×20%, 30%, 40%, and FDG ×40% showed similar lesion lengths compared with that in endoscopic examination (P > 0.05). GTV<sub>CT</sub> demonstrated the largest volume (median: 48.80 mm<sup>3</sup>, range: 14.83-162.23 mm<sup>3</sup>) than PET-based GTVs. For PET/CT-guided complementary contouring of GTV<sub>CT</sub>, four patients (19%) were increased by FAPI ×20% and 30%, two patients (9.5%) were increased by FAPI ×40%, and only one patient was increased by FDG ×40%. Furthermore, the volume of GTV based on CE-CT plus FAPI ×20%, 30%, and 40% showed no significant difference with GTV<sub>CT</sub> and planning target volume based CE-CT plus FAPI-PET and meets the organ at risk standard. The <sup>68</sup>Ga-FAPI PET/CT methodology showed favourable tumour-to-background contrast in oesophageal cancer and might provide additional information for target volume delineation and help avoid tumour geographic misses.

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