Abstract 1458P
Background
68Ga-labeled fibroblast activation protein inhibitor (FAPI) positron emission tomography (PET)/computed tomography (CT) has been shown to be advantageous in the detection of primary and metastatic lesions in many types of tumors, especially gastric cancer. However, there is a paucity of data on the value of 68Ga-FAPI-04 PET/CT for initial staging, recurrence detection after surgery and management of gastric cancer patients.
Methods
114 patients with gastric cancer who underwent contrast-enhanced CT and 68Ga-FAPI-04 PET/CT within one months were included. Two nuclear medicine physicians and a radiologist independently reviewed the imaging. TNM staging outcomes and subsequent treatment decisions were compared between contrast-enhanced CT and 68Ga-FAPI-04 PET/CT.
Results
84 patients underwent 68Ga-FAPI-04 PET/CT scans for initial staging, comprising 12 with stage II, 44 with stage III, and 28 with stage IV as per CT staging. Furthermore, 30 postoperative patients underwent PET-CT scanning in the presence of clinical symptoms, abnormal laboratory tests, and ambiguous CT findings. PET-CT revealed 29 newly metastatic lesions, with distant lymph nodes (12 occurrences) and peritoneal lesions (11 occurrences) being the most frequently observed. 68Ga-FAPI-04 PET/CT revised staging in 22/114 patients (19.3%). Among those, downstaging was recorded in 4/22 cases (18.2%) and upstaging in the remaining 18/22 (81.8%) patients. Overall, the findings of 68Ga-FAPI-04 PET/CT led to a change in clinical management in 15/114 patients (13.1%), including 12 instances of major and 3 instances of minor therapeutic changes. In 30 postoperative patients, 8 cases (26.3%) had recurrent metastasis, leading to 13.3% management change. Among 84 initial staging patients, 14 cases (16.7%) had staging change, resulting in 13.1% management change.
Conclusions
68Ga-FAPI-04 PET/CT proved to be a valuable tool for precise staging of gastric cancer patients. 68Ga-FAPI-04 PET/CT promises to improve conventional radiologic imaging methods for gastric cancer staging.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1525P - Nab-paclitaxel/gemcitabine with or without epigenetic targeting followed by consolidating immune targeting with durvalumab and lenalidomide in patients with advanced pancreatic ductal adenocarcinoma: Results from the SEPION/AIO-PAK-0118 phase I/II study
Presenter: Jens Siveke
Session: Poster session 18
1527P - GnP vs mFOLFIRINOX or S-IROX in metastatic pancreatic cancer: 1-year follow-up updated data from the GENERATE (JCOG1611)
Presenter: Satoshi Kobayashi
Session: Poster session 18
1528P - TCOG T5221 trial: A phase II randomized study of gemcitabine and nab-paclitaxel in combination with S- 1/LV (GASL) or oxaliplatin (GAP) as first-line treatment for metastatic pancreatic cancer
Presenter: Yung-yeh Su
Session: Poster session 18
1531TiP - TWINPEAK phase I/II study, PT886 a bispecific antibody targeting claudin 18.2 and CD47 in combination with chemotherapy and/or pembrolizumab in gastric/GEJ-carcinomas or PDAC
Presenter: Michael Overman
Session: Poster session 18
1532TiP - Zolbetuximab with gemcitabine + nab-paclitaxel (GN) in first-line treatment of Claudin 18.2–positive metastatic pancreatic cancer (mPC): Phase II, open-label, randomized study
Presenter: Wungki Park
Session: Poster session 18
1533TiP - A multicenter, open-label phase II study to evaluate the efficacy and safety of pimicotinib (CSF-1R inhibitor) in combination with chemotherapy with or without toripalimab in patients (pts) with advanced pancreatic ductal adenocarcinoma (aPDAC)
Presenter: Xiaofei Zhang
Session: Poster session 18
1534TiP - Valproic acid combinEd with Simvastatin and gemcitabine/nab-paclitaxel-based regimens in untreated metastatic Pancreatic Adenocarcinoma patients-VESPA trial
Presenter: Alfredo Budillon
Session: Poster session 18