RT Journal Article SR Electronic T1 [18F]mFBG Long Axial Field Of View (LAFOV) PET/CT without sedation or general anaesthesia compared to [123I]mIBG scintigraphy with single-photon emission computed tomography-CT (SPECT/CT) for imaging of children with neuroblastoma. JF Journal of Nuclear Medicine JO J Nucl Med FD Society of Nuclear Medicine SP P1313 OP P1313 VO 64 IS supplement 1 A1 Borgwardt, Lise A1 brok, jesper A1 Andersen, Kim Francis A1 Madsen, Jacob A1 Gillings, Nicholas A1 Fosbøl, Marie A1 denholt, charlotte A1 Enevoldsen, lotte A1 Oturai, Peter A1 Johannesen, Helle A1 Czyzewska, Dorota A1 Højgaard, Liselotte A1 Andersen, Flemming A1 Fischer, Barbara YR 2023 UL http://jnm.snmjournals.org/content/64/supplement_1/P1313.abstract AB P1313 Introduction: Meta-[18F]fluorobenzylguanidine ([18F]mFBG) is a new positron emission tomography (PET) radiotracer that allows for fast and high-resolution imaging of tumours expressing the norepinephrine transporter. These initial results investigates the value of [18F]mFBG Long Axial Field Of View (LAFOV) PET/CT compared to 'standard' [123I]mIBG scintigraphy with single-photon emission computed tomography-CT (SPECT/CT) for imaging in neuroblastoma.Methods: Prospective, single-center study, that recruited children with neuroblastoma, referred for meta-[123I]iodobenzylguanidine ([123I]mIBG) whole body planar scintigraphy with SPECT/CT of the thorax and abdomen. Within 1 week of [123I]mIBG scintigraphy, [18F]mFBG LAFOV PET/CT (Siemens Vision Quadra PET/CT) were performed at 1 h p.i. of [18F]mFBG (1.5-3 MBq/kg) without sedation or general anaesthesia (GA). The PET acquisition time was 10 min., if possible for the child, with only 2 min. of reconstruction required (being the minimum required scanning time in order to provide a clinically useful image) and by scanning 10 min. the periods without motion artefacts could be reconstructed. Tumour localisation and extension on paired scan were compared.Results: 16 paired [123I]mIBG and [18F]mFBG scans were performed in 8 patients (median age 3.25 years (0.25-8.08 y), n = 2 stage L2(low risk), n=1 stage L2(intermediate risk), n=1 stage L2(high risk/relaps), n=2 stage M (high risk), n=1 stage M (high risk/relaps), n=1 stage MS. Mean scan time for [18F]mFBG PET-CT (7.7 min, SD 2.6) was significantly shorter than for [123I]mIBG scanning (72.5 min, SD 16.3), p < 0.01. None of the children had sedation or GA during the PET scanning procedure, whereas 81% had GA during the [123I]mIBG scintigraphy with SPECT/CT. Compared to [123I]mIBG scintigraphy, [18F]mFBG PET-CT detected a higher, equal, and lower number of avid lesions in 75%, 25%, and 0% of scan pairs, respectively. Especially, intraspinal-, retroperitoneal lymph node-, and bone marrow involvement is diagnosed with much higher accuracy in [18F]mFBG LAFOV PET/CT compared to [123I]mIBG scintigraphy with SPECT/CT.Conclusions: Preliminary results demonstrate that more neuroblastoma localisations were detected on [18F]mFBG LAFOV PET/CT compared to [123I]mIBG scintigraphy with SPECT/CT. The clinical benefit of [18F]mFBG LAFOV PET/CT is a 1 day protocol, much shorter scan time and avoidance of GA/sedation in most patients. [18F]mFBG LAFOV PET/CT shows promise for future staging and response assessment in neuroblastoma in children.