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A Practical Guide for the Production and PET/CT Imaging of 68Ga-DOTATATE for Neuroendocrine Tumors in Daily Clinical Practice
Published on: April 17, 2019
Pathological validation of 18F-AlF-NOTA-octreotide PET/CT for neuroblastoma
Yuxuan Liu1, Yuting Ma2, Han Wang1
1Department of Nuclear Medicine, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical Sciences, Jinan, 250117, Shandong, China.
Abstract:
Somatostatin receptor 2 (SSTR2) positron emission tomography/computed tomography (PET/CT) plays an important role in the diagnosis and treatment of neuroblastoma (NB), but it faces the issue of nonspecific uptake. Although the relationship between SSTR PET/CT and SSTR2 expression has been studied in neuroendocrine tumours (NETs), significant differences exist between NB and NETs, and the application of 18F-AlF-NOTA-octreotide (18F-OC) PET/CT in NB requires further investigation. This retrospective study assessed the relationship between 18F-OC PET/CT imaging parameters and immunohistochemical (IHC) scores for the quantification of SSTR2 expression in NB. We obtained imaging and clinical data from patients with initial or treated NB who underwent 18F-OC PET/CT at Shandong Cancer Hospital between June 2021 and March 2023. Pathologically validated and accurately localized lesions on PET/CT images were analysed. 18F-OC uptake was assessed using Krenning scores, maximum (SUVmax) and mean (SUVmean) standardized uptake values. We determined SSTR2 expression by evaluating scores for human epidermal growth factor receptor 2 (HER2) score, immunoreactive score (IRS), histochemical score (H score), and Volante score. We analysed 71 lesions (NB, n = 51), NB that converted to ganglioneuroblastoma (GNB) after treatment (n = 9), and ganglioneuromas (GN, n = 11). SSTR2 scores and 18F-OC uptake were significantly higher in NB tumours than in GNB and GN tumours. Furthermore, 77.9% of 18F-OC PET/CT-positive lesions were SSTR2-positive by IHC, and imaging parameters were significantly positively correlated with HER2 score, IRS, and H score in the total cohort and the NB group (Rho range, 0.433-0.602; p < 0.000). No significant correlation was observed between imaging parameters and pathological scores in GNB and GN tumours (p > 0.05).There was high agreement between 18F-OC PET/CT imaging and SSTR2 IHC scores in newly diagnosed and residual NB tumours and no significant correlation between these two methods in GNB and GN tumours. These results indicate that PET/CT providing molecular evidence for future follow-up and guidance for NB treatment.
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