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| 100 | 1 | _ | |a Bartel, Timo |0 P:(DE-HGF)0 |b 0 |
| 245 | _ | _ | |a [68Ga]Ga-FAPI-46 PET/CT of Patients with Gastrointestinal Stromal Tumors in Comparison to 2-[18F]FDG PET/CT and Contrast-Enhanced CT: Results from a Prospective Observational Study. |
| 260 | _ | _ | |a New York, NY |c 2026 |b Soc. |
| 336 | 7 | _ | |a article |2 DRIVER |
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| 500 | _ | _ | |a 2026 Feb 2;67(2):210-216 |
| 520 | _ | _ | |a Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal neoplasms of the gastrointestinal tract. Although contrast-enhanced CT (ceCT) and 2-[18F]FDG PET/CT remain standard imaging modalities, both exhibit limitations in detecting small peritoneal metastases and tumors with low metabolic activity. 68Ga-labeled fibroblast activation protein inhibitors (FAPIs) have shown promising results in various malignancies; however, comparative data on GISTs are limited. This study aimed to assess the diagnostic performance of [68Ga]Ga-FAPI-46 PET/CT in comparison with 2-[18F]FDG PET/CT and ceCT, including evaluation of interreader reproducibility and clinical impact. Methods: This study retrospectively reviewed 25 patients with histopathologically confirmed GISTs undergoing [68Ga]Ga-FAPI-46 PET/CT as part of a prospective observational study (NCT04571086). All patients (n = 25) underwent additional clinical 2-[18F]FDG PET/CT; ceCT was performed for 23 of 25 patients. Imaging was assessed per patient and per region (primary tumor, lymph nodes, and visceral and bone metastases), and a composite reference standard that included histopathology, follow-up imaging, and clinical data was applied. Interreader agreement, stratified by experience level, was analyzed using Cohen κ (κCohen). Referring physicians completed questionnaires before and after imaging to determine clinical impact. Results: In total, 28 validated regions (n = 20 patients) were included in the diagnostic efficacy analysis. Per region, ceCT and [68Ga]Ga-FAPI-46 PET/CT demonstrated comparable sensitivity (83% vs. 81%), followed by 2-[18F]FDG PET/CT (65%). [68Ga]Ga-FAPI-46 PET/CT demonstrated the highest region-based positive predictive value (100%). The liver tumor-to-background ratio was significantly higher for [68Ga]Ga-FAPI-46 PET/CT than for 2-[18F]FDG PET/CT (median, 7.6 vs. 5.9; P = 0.034), whereas overall tumor uptake showed no significant difference. Changes in clinical management attributable to [68Ga]Ga-FAPI-46 PET/CT were observed for 6 of 24 patients (25%), including 1 major change. Interreader agreement for [68Ga]Ga-FAPI-46 PET/CT varied with reader experience, showing the highest concordance between high- and intermediate-experience readers (κCohen = 0.87 per patient and 0.47-1.00 across regions), whereas comparisons involving less experienced readers yielded lower agreement (κCohen = 0.00-0.60). Conclusion: [68Ga]Ga-FAPI-46 PET/CT demonstrated diagnostic sensitivity comparable to ceCT and superior to 2-[18F]FDG PET/CT for patients with GISTs. High diagnostic performance, especially in hepatic and peritoneal metastases, and relevant clinical impact support a role for [68Ga]Ga-FAPI-46 PET/CT as complementary imaging modality. |
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| 650 | _ | 7 | |a 2-[18F]FDG PET/CT |2 Other |
| 650 | _ | 7 | |a GIST |2 Other |
| 650 | _ | 7 | |a [68Ga]Ga-FAPI-46 PET/CT |2 Other |
| 650 | _ | 7 | |a detection efficacy |2 Other |
| 700 | 1 | _ | |a Pabst, Kim M |0 P:(DE-HGF)0 |b 1 |
| 700 | 1 | _ | |a Barg, Christina |0 P:(DE-HGF)0 |b 2 |
| 700 | 1 | _ | |a Berliner, Christoph A |0 P:(DE-HGF)0 |b 3 |
| 700 | 1 | _ | |a Hamacher, Rainer |0 P:(DE-HGF)0 |b 4 |
| 700 | 1 | _ | |a Bauer, Sebastian |0 P:(DE-HGF)0 |b 5 |
| 700 | 1 | _ | |a Falkenhorst, Johanna |0 P:(DE-HGF)0 |b 6 |
| 700 | 1 | _ | |a Kessler, Lukas |0 P:(DE-HGF)0 |b 7 |
| 700 | 1 | _ | |a Nader, Michael |0 P:(DE-HGF)0 |b 8 |
| 700 | 1 | _ | |a Barbato, Francesco |0 P:(DE-HGF)0 |b 9 |
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| 700 | 1 | _ | |a Herrmann, Ken |0 P:(DE-HGF)0 |b 11 |
| 700 | 1 | _ | |a Fendler, Wolfgang P |0 P:(DE-HGF)0 |b 12 |
| 773 | _ | _ | |a 10.2967/jnumed.125.270850 |g p. jnumed.125.270850 - |0 PERI:(DE-600)2040222-3 |n 2 |p 210-216 |t Journal of nuclear medicine |v 67 |y 2026 |x 0097-9058 |
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