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[(18)F]mFBG PET-CT for detection and localisation of neuroblastoma: a prospective pilot study
PURPOSE: Meta-[(18)F]fluorobenzylguanidine ([(18)F]mFBG) is a positron emission tomography (PET) radiotracer that allows for fast and high-resolution imaging of tumours expressing the norepinephrine transporter. This pilot study investigates the feasibility of [(18)F]mFBG PET-CT for imaging in neuro...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931849/ https://www.ncbi.nlm.nih.gov/pubmed/36504277 http://dx.doi.org/10.1007/s00259-022-06063-6 |
Sumario: | PURPOSE: Meta-[(18)F]fluorobenzylguanidine ([(18)F]mFBG) is a positron emission tomography (PET) radiotracer that allows for fast and high-resolution imaging of tumours expressing the norepinephrine transporter. This pilot study investigates the feasibility of [(18)F]mFBG PET-CT for imaging in neuroblastoma. METHODS: In a prospective, single-centre study, we recruited children with neuroblastoma, referred for meta-[(123)I]iodobenzylguanidine ([(123)I]mIBG) scanning, consisting of total body planar scintigraphy in combination with single-photon emission computed tomography-CT (SPECT-CT). Within two weeks of [(123)I]mIBG scanning, total body PET-CTs were performed at 1 h and 2 h after injection of [(18)F]mFBG (2 MBq/kg). Detected tumour localisations on scan pairs were compared. Soft tissue disease was quantified by number of lesions and skeletal disease by SIOPEN score. RESULTS: Twenty paired [(123)I]mIBG and [(18)F]mFBG scans were performed in 14 patients (median age 4.9 years, n = 13 stage 4 disease and n = 1 stage 4S). [(18)F]mFBG injection was well tolerated and no related adverse events occurred in any of the patients. Mean scan time for [(18)F]mFBG PET-CT (9.0 min, SD 1.9) was significantly shorter than for [(123)I]mIBG scanning (84.5 min, SD 10.5), p < 0.01. Most tumour localisations were detected on the 1 h versus 2 h post-injection [(18)F]mFBG PET-CT. Compared to [(123)I]mIBG scanning, [(18)F]mFBG PET-CT detected a higher, equal, and lower number of soft tissue lesions in 40%, 55%, and 5% of scan pairs, respectively, and a higher, equal, and lower SIOPEN score in 55%, 30%, and 15% of scan pairs, respectively. On average, two more soft tissue lesions and a 6-point higher SIOPEN score were detected per patient on [(18)F]mFBG PET-CT compared to [(123)I]mIBG scanning. CONCLUSION: Results of this study demonstrate feasibility of [(18)F]mFBG PET-CT for neuroblastoma imaging. More neuroblastoma localisations were detected on [(18)F]mFBG PET-CT compared to [(123)I]mIBG scanning. [(18)F]mFBG PET-CT shows promise for future staging and response assessment in neuroblastoma. TRIAL REGISTRATION: Dutch Trial Register NL8152. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00259-022-06063-6. |
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