background: positron emission tomography/computed tomography (PET/CT) with 18F-fluorodeoxyglucose (18F-FDG) is a firmly established tool in oncology and is gaining importance in dermato-oncology. however, its use in advanced basal cell carcinoma (BCC) is limited, with only a few case reports and a single study focused on vismodegib. this study evaluates the role of 18F-FDG PET/CT in advanced BCC treated with sonidegib. methods: we retrospectively assessed the clinical data of patients with advanced BCC who underwent 18F-FDG PET/CT between January 2022 and January 2024. Inclusion criteria included histologically confirmed BCC, FDG-avid lesions on baseline PET/CT, and a minimum follow-up of 6 months. metabolic response was assessed using the PET response criteria in solid tumors (PERCIST). results: four patients with advanced BCC treated with sonidegib were included, presenting with a total of 10 hypermetabolic lesions at baseline PET/CT. the mean interval between baseline and follow-up scans was 8.7 +/- 1.6 months. according to percist, two patients achieved a complete metabolic response (CMR), while the other two had stable metabolic disease (SMD). low baseline-standardized uptake values (i.e., SUVmax, SUVmean) and reduced total lesion glycolysis (TLG) were associated with CMR. no relapses were observed during follow-up. conclusions: this study suggests that 18F-FDG PET/CT may help identify advanced BCC patients who are likely to benefit from sonidegib treatment. further research is needed to fully explore the potential of PET/CT in this specific clinical context.

Proietti, I., Filippi, L., Bagni, O., Potenza, C. (2024). Metabolic Imaging of Advanced Basal Cell Carcinoma Treated with Sonidegib: A Retrospective Case Series Study. JOURNAL OF CLINICAL MEDICINE, 13(17) [10.3390/jcm13175087].

Metabolic Imaging of Advanced Basal Cell Carcinoma Treated with Sonidegib: A Retrospective Case Series Study

Luca Filippi;
2024-01-01

Abstract

background: positron emission tomography/computed tomography (PET/CT) with 18F-fluorodeoxyglucose (18F-FDG) is a firmly established tool in oncology and is gaining importance in dermato-oncology. however, its use in advanced basal cell carcinoma (BCC) is limited, with only a few case reports and a single study focused on vismodegib. this study evaluates the role of 18F-FDG PET/CT in advanced BCC treated with sonidegib. methods: we retrospectively assessed the clinical data of patients with advanced BCC who underwent 18F-FDG PET/CT between January 2022 and January 2024. Inclusion criteria included histologically confirmed BCC, FDG-avid lesions on baseline PET/CT, and a minimum follow-up of 6 months. metabolic response was assessed using the PET response criteria in solid tumors (PERCIST). results: four patients with advanced BCC treated with sonidegib were included, presenting with a total of 10 hypermetabolic lesions at baseline PET/CT. the mean interval between baseline and follow-up scans was 8.7 +/- 1.6 months. according to percist, two patients achieved a complete metabolic response (CMR), while the other two had stable metabolic disease (SMD). low baseline-standardized uptake values (i.e., SUVmax, SUVmean) and reduced total lesion glycolysis (TLG) were associated with CMR. no relapses were observed during follow-up. conclusions: this study suggests that 18F-FDG PET/CT may help identify advanced BCC patients who are likely to benefit from sonidegib treatment. further research is needed to fully explore the potential of PET/CT in this specific clinical context.
2024
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MEDS-22/A - Diagnostica per immagini e radioterapia
English
PET/CT
advanced basal cell carcinoma
hedgehog pathway inhibitors
metabolic imaging
oncology
quantitative parameters
Proietti, I., Filippi, L., Bagni, O., Potenza, C. (2024). Metabolic Imaging of Advanced Basal Cell Carcinoma Treated with Sonidegib: A Retrospective Case Series Study. JOURNAL OF CLINICAL MEDICINE, 13(17) [10.3390/jcm13175087].
Proietti, I; Filippi, L; Bagni, O; Potenza, C
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/391265
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