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Improved Localization of Insulinomas Using 68Ga-NODAGA-Exendin-4 PET/CT

Boss, M; Eriksson, O; Mikkola, K; Eek, A; Brom, M; Buitinga, M; Brouwers, AH; Velikyan, I; Waser, B; Kauhanen, S; Solin, O; Marciniak, C; Eriksson, B; Reubi, JC; Aveline, C; Wild, D; Pattou, F; Talbot, JN; Hofland, J; Sundin, A; Nuutila, P; Hermans, J; Gotthardt, M

Improved Localization of Insulinomas Using 68Ga-NODAGA-Exendin-4 PET/CT

Boss, M
Eriksson, O
Mikkola, K
Eek, A
Brom, M
Buitinga, M
Brouwers, AH
Velikyan, I
Waser, B
Kauhanen, S
Solin, O
Marciniak, C
Eriksson, B
Reubi, JC
Aveline, C
Wild, D
Pattou, F
Talbot, JN
Hofland, J
Sundin, A
Nuutila, P
Hermans, J
Gotthardt, M
Katso/Avaa
1959.full.pdf (894.2Kb)
Lataukset: 

Society of Nuclear Medicine
doi:10.2967/jnumed.124.268158
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2025082790797
Tiivistelmä

Precise anatomic localization of insulinomas is crucial for surgical treatment. Current routine noninvasive imaging techniques, including CT, MRI, and 68Ga-DOTA-somatostatin analog (DOTA-SSA) PET/CT, have limited sensitivity. Endoscopic ultrasound is highly sensitive but invasive. In this prospective multicenter study, we compared the diagnostic accuracy of 68Ga-NODAGA-exendin-4 (exendin) PET/CT with all routine imaging procedures for the localization of insulinomas.

Methods: Sixty-nine adults with biochemically proven adult endogenous hyperinsulinemic hypoglycemia underwent exendin PET/CT and current routine imaging. Images were evaluated in a clinical reading and in an expert reading. Image quality was determined by quantitative analysis.

Results: Based on clinical readings, the accuracy of exendin PET/CT (94.4%; 95% CI, 84.6%-98.8%) was greater than that of DOTA-SSA PET/CT (64.8%; 95% CI, 50.6%-77.3%), contrast-enhanced CT/contrast-enhanced diffusion-weighted imaging-MRI (83.3%; 95% CI, 70.7%-92.1%), and endoscopic ultrasound (82.8%; 95% CI, 64.1%-94.1%). In 13% of patients, a correct diagnosis was only reached after exendin PET/CT. Interobserver agreement between readings was higher for exendin PET/CT than for DOTA-SSA PET/CT and contrast-enhanced CT/contrast-enhanced diffusion-weighted imaging-MRI (Cohen κ, 1.0 vs. 0.5 and 0.55). Exendin PET/CT provided a higher insulinoma-to-background ratio (15.3 ± 6.7 vs. 5.2 ± 3.0) and contrast-to-noise ratio (22.6 ± 11.1 vs. 5.1 ± 3.7) than did DOTA-SSA PET/CT.

Conclusion: This study demonstrates the superiority of exendin PET/CT in a unique prospective comparison to all current routine imaging modalities for preoperative localization of benign insulinomas, providing the level of evidence needed for clinical implementation.

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