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Prognostic value of fibroblast activation protein expressing tumor volume calculated from [68 Ga]Ga-FAPI PET/CT in patients with esophageal squamous cell carcinoma

Background This study aimed to investigate the prognostic value of semiquantitative parameters derived from [ 68  Ga]Ga-fibroblast activation protein inhibitor (FAPI) PET/CT for patients with esophageal squamous cell carcinoma (ESCC) treated with definitive chemoradiotherapy. Methods We conducted a...

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Bibliographic Details
Published in:European journal of nuclear medicine and molecular imaging 2023, Vol.50 (2), p.593-601
Main Authors: Zhao, Liang, Pang, Yizhen, Chen, Shanyu, Chen, Jianhao, Li, Yimin, Yu, Yifeng, Huang, Chunbin, Sun, Long, Wu, Hua, Chen, Haojun, Lin, Qin
Format: Article
Language:English
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Summary:Background This study aimed to investigate the prognostic value of semiquantitative parameters derived from [ 68  Ga]Ga-fibroblast activation protein inhibitor (FAPI) PET/CT for patients with esophageal squamous cell carcinoma (ESCC) treated with definitive chemoradiotherapy. Methods We conducted a retrospective analysis on patients from a prospective parent study (NCT04416165). A total of 45 patients with locally advanced ESCC who underwent [ 68  Ga]Ga-FAPI from December 2019 to March 2021 were included. The maximum standard uptake value (SUVmax), gross tumor volume (GTV), and total lesion-FAPI (TL-FAPI) of the primary tumor were calculated from the corresponding PET/CT image. Unpaired parameters were compared using Student’s t test or the Mann–Whitney U test. Paired parameters were compared using the paired t test or the Wilcoxon matched-pairs signed-rank test. Kaplan–Meier curves were generated to calculate progression-free survival (PFS) and overall survival (OS) rates, and Cox regression analysis was performed to determine which PET/CT parameters were prognostic factors for PFS and/or OS. Results Thirty-four of the 45 patients met the criteria, and the median follow-up time was 24 months (16–29 months). SUVmax-FAPI, GTV FAPI , and TL-FAPI in patients with stage T4 tumors were significantly higher than those in patients with stage T2/T3 tumors (all P  
ISSN:1619-7070
1619-7089
DOI:10.1007/s00259-022-05989-1