J Thorac Dis
The First Affiliated Hospital of Jinan University, Guangzhou, China.
Published: February 2025
Background: Fluorine 18-labeled fibroblast activation protein inhibitor (F-FAPI-04) positron emission tomography/computed tomography (PET/CT) has shown promise for the visualization of advanced stage lung cancer. The accuracy of F-FAPI-04 compared with that of fluorine-18 labeled-fluorodeoxyglucose (F-FDG) in detecting early lung adenocarcinoma (LUAD) remains unknown. Taking the surgical pathology of pulmonary nodule as the gold standard, the diagnostic performance of stage IA LUAD were compared between F-FAPI-04 PET/CT and F-FDG PET/CT, and the correlation between F-FAPI-04 uptake and pathological characteristics of stage IA LUAD.
Methods: This prospective study from February 2023 to October 2023 analyzed patients with stage IA LUAD who underwent simultaneous examinations with F-FAPI-04 and F-FDG PET/CT. Semi-quantitative parameters such as maximum standardized uptake value (SUVmax), tumor-to-background ratio (TBR), metabolic tumor volume (MTV), total lesion glycolysis (TLG), FAPI avid tumor volume (FTV), and total lesion FAP expression (TLF) were calculated. The two patterns were compared using either a paired Student's -test or a Wilcoxon signed-rank test. Immunohistochemical (IHC) staining for detecting fibroblast activating protein (FAP) expression was performed in all resected tumor specimens. Correlation analysis was performed between F-FAPI-04 uptake and pathological features of stage IA LUAD.
Results: A total of 20 patients diagnosed with stage IA LUAD were included in this study. A total of 24 pulmonary nodules were identified in these 20 patients, all of whom were confirmed to have stage IA LUAD through operation and pathology. Of them, 17 nodules were stained by FAP immunohistochemistry. Compared with F-FDG, F-FAPI-04 PET/CT showed a statistically significant increase in SUVmax and TBR for stage IA LUAD, both in the overall and stratified analyses (adenocarcinoma + minimally invasive adenocarcinoma groups invasive adenocarcinoma groups; moderately well-differentiated lesions; stage IA1 IA2+3; P<0.05). The SUVmax of the intense FAP expression group was significantly higher than that of the mild FAP expression group, demonstrating a statistically significant difference (P=0.005). The FAP-IHC score was positively correlated with the SUVmax of F-FAPI-04 (r=0.64, P=0.005).
Conclusions: F-FAPI-04 PET/CT demonstrates higher SUVmax and TBR than F-FDG PET/CT in the detection of stage IA LUAD. It was re-assured that the F-FAPI-04 uptake of stage IA LUAD was positively correlated with the expression of FAP .
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http://dx.doi.org/10.21037/jtd-24-1658 | DOI Listing |
Nucl Med Commun
March 2025
Graduate Joint Training Base, Zhejiang Chinese Medical University.
Background: This study aimed to investigate the prognostic value of baseline total metabolic tumor volume (TMTV) on 18F-fluorodeoxyglucose positron emission tomography/computed tomography and its potential for further stratification within the ninth tumor-node-metastasis (TNM) staging system in patients with lung adenocarcinoma (LUAD).
Methods: A cohort of 384 patients with LUAD who had undergone pretreatment PET/CT were included in this retrospective study. The optimal cutoff value for TMTV was determined through analysis of time-dependent receiver operating characteristic curves.
Background: Fluorine 18-labeled fibroblast activation protein inhibitor (F-FAPI-04) positron emission tomography/computed tomography (PET/CT) has shown promise for the visualization of advanced stage lung cancer. The accuracy of F-FAPI-04 compared with that of fluorine-18 labeled-fluorodeoxyglucose (F-FDG) in detecting early lung adenocarcinoma (LUAD) remains unknown. Taking the surgical pathology of pulmonary nodule as the gold standard, the diagnostic performance of stage IA LUAD were compared between F-FAPI-04 PET/CT and F-FDG PET/CT, and the correlation between F-FAPI-04 uptake and pathological characteristics of stage IA LUAD.
View Article and Find Full Text PDFFront Pharmacol
February 2025
Department of General Internal Medicine, Tianjin Hospital, Tianjin, China.
Background: is expressed in various tumors and leukemia cell lines. This study aims to explore the effect of in lung adenocarcinoma (LUAD).
Methods: The data on LUAD patients were collected from the Cancer Genome Atlas and Gene Expression Omnibus database.
Nat Commun
March 2025
Central Laboratory, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, 200433, China.
Lung adenocarcinoma (LUAD) radiologically displayed as subsolid nodules (SSNs) is prevalent. Nevertheless, the precise clinical management of SSNs necessitates a profound understanding of their tumorigenesis and progression. Here, we analyze 66 LUAD displayed as SSNs covering 3 histological stages including adenocarcinoma in situ (AIS), minimally invasive adenocarcinoma (MIA) and invasive adenocarcinoma (IAC) by incorporating genomics, proteomics, phosphoproteomics and glycoproteomics.
View Article and Find Full Text PDFRespir Res
March 2025
Department of Radiology, The Xuzhou Hospital Affiliated to Jiangsu University, Xuzhou Cancer Hospital, Xuzhou, People's Republic of China.
Background: To evaluate the clinical applicability of deep learning (DL) models based on automatic segmentation in preoperatively predicting tumor spread through air spaces (STAS) in peripheral stage I lung adenocarcinoma (LUAD).
Methods: This retrospective study analyzed data from patients who underwent surgical treatment for lung tumors from January 2022 to December 2023. An external validation set was introduced to assess the model's generalizability.
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