The aim of the present study is to investigate the synergic role of ⁶⁸Ga-PSMA PET/MRI and ⁶⁸Ga-DOTA-RM2 PET/MRI in prostate cancer (PCa) staging. We present pilot data on twenty-two patients with biopsy-proven PCa that underwent ⁶⁸Ga-PSMA PET/MRI for staging purposes, with 19/22 also undergoing ⁶⁸Gaa-DOTA-RM2 PET/MRI. TNM classification based on image findings was performed and quantitative imaging parameters were collected for each scan. Furthermore, twelve patients underwent radical prostatectomy with the availability of histological data that were used as the gold standard to validate intraprostatic findings. A DICE score between regions of interest manually segmented on the primary tumour on ⁶⁸Ga-PSMA PET, ⁶⁸Ga-DOTA-RM2 PET and on T2 MRI was computed. All imaging modalities detected the primary PCa in 18/19 patients, with ⁶⁸Ga-DOTA-RM2 PET not detecting any lesion in 1/19 patients. In the remaining patients, ⁶⁸Ga-PSMA and MRI were concordant. Seven patients presented seminal vesicles involvement on MRI, with two of these being also detected by ⁶⁸Ga-PSMA, and ⁶⁸Ga-DOTA-RM2 PET being negative. Regarding extraprostatic disease, ⁶⁸Ga-PSMA PET, ⁶⁸Ga-DOTA-RM2 PET and MRI resulted positive in seven, four and five patients at lymph-nodal level, respectively, and at a bone level in three, zero and one patients, respectively. These preliminary results suggest the potential complementary role of ⁶⁸Ga-PSMA PET, ⁶⁸Ga-DOTA-RM2 PET and MRI in PCa characterization during the staging phase.

Axillary surgery in breast cancer (BC) is no longer a therapeutic procedure but has become a purely staging procedure. The progressive improvement in imaging techniques has paved the way to the hypothesis that prognostic information on nodal status deriving from surgery could be obtained with an accurate diagnostic exam. Positron emission tomography/magnetic resonance imaging (PET/MRI) is a relatively new imaging tool and its role in breast cancer patients is still under investigation. We reviewed the available literature on PET/MRI in BC patients. This overview showed that PET/MRI yields a high diagnostic performance for the primary tumor and distant lesions of liver, brain and bone. In particular, the results of PET/MRI in staging the axilla are promising. This provided the rationale for two prospective comparative trials between axillary surgery and PET/MRI that could lead to a further de-escalation of surgical treatment of BC. • SNB vs. PET/MRI 1 trial compares PET/MRI and axillary surgery in staging the axilla of BC patients undergoing primary systemic therapy (PST). • SNB vs. PET/MRI 2 trial compares PET/MRI and sentinel node biopsy (SNB) in staging the axilla of early BC patients who are candidates for upfront surgery. Finally, these ongoing studies will help clarify the role of PET/MRI in BC and establish whether it represents a useful diagnostic tool that could guide, or ideally replace, axillary surgery in the future.

The initial characterization of the first SPECT insert for simultaneous human brain imaging inside MRI is presented. The instrument features a novel multi-mini slit-slat collimator and a static ring of 20 detectors. The scanner architecture is modular and represents the scale-up of a preclinical version whose MRI-compatibility has been already successfully demonstrated. The detectors are based on CsI(Tl) crystals (50 mm × 100 mm × 8 mm) coupled to arrays of SiPMs and ASIC readout for a total of 1440 channels. The transaxial FoV is 20 cm by 9 cm in the axial direction. The experimental results show a sensitivity of 362 cps/MBq, an energy resolution of 17% (at 140 keV) and a tomographic extrinsic resolution in the transaxial plane of 8 mm across the whole FoV.

Purpose: Personalized treatment schemes are being systematically applied to ensure best treatment outcome in oncologic patients. This is true also for personalized dosimetry in transarterial radioembolization (TARE) in hepatocellular carcinoma (HCC) patients. Precise and detailed volumetric and functional data derived from radiological and nuclear imaging methods are essential for personalized dosimetry. We sought to evaluate accuracy of dual-phase cone-beam CT (CBCT) in comparison to pre-treatment contrast-enhanced CT (CECT), and ^99mTc-macroaggregated albumin-SPECT/CT ([^99mTc]MAA SPECT/CT) to predict and assess the efficacy of TARE based on post-treatment ⁹⁰Y PET/CT. Material and methods: Thirty consecutive patients with HCC treated with TARE were included. Intraprocedural dual-phase CBCT acquisition protocol was developed to distinguish tumor volume in the early arterial phase and perfused volume of non-affected liver in the late arterial phase. Volumetric data obtained from pre-treatment CECT, dual-phase CBCT and [^{99 m}Tc]MAA SPECT/CT were compared to post-treatment ⁹⁰Y PET/CT considered the standard reference. Treatment simulations for final calculated dose from the different imaging derived volumes were then compared to post-treatment ⁹⁰Y PET/CT. Results: CBCT resulted as the most accurate method in predicting tumor- (R² 0.89) and perfused volumes (R² 0.84). Dosimetry prediction planning performed on derived volumes from the different methods did not show significant difference, yet highest concordance with ⁹⁰Y PET/CT data was observed with dual-phase CBCT. Conclusion: Our study shows that dual-phase CBCT acquisition is a novel alternative method for correctly and safely administering more accurate and defined doses during TARE. clinicaltrials.gov ID: NCT03981497.

This study proposed a new workflow for co-registering prostate PET images from a dual-tracer PET/MRI study with histopathological images of resected prostate specimens. The method aims to establish an accurate correspondence between PET/MRI findings and histology, facilitating a deeper understanding of PET tracer distribution and enabling advanced analyses like radiomics. To achieve this, images derived by three patients who underwent both [⁶⁸Ga]Ga-PSMA and [⁶⁸Ga]Ga-RM2 PET/MRI before radical prostatectomy were selected. After surgery, in the resected fresh specimens, fiducial markers visible on both histology and MR images were inserted. An ex vivo MRI of the prostate served as an intermediate step for co-registration between histological specimens and in vivo MRI examinations. The co-registration workflow involved five steps, ensuring alignment between histopathological images and PET/MRI data. The target registration error (TRE) was calculated to assess the precision of the co-registration. Furthermore, the DICE score was computed between the dominant intraprostatic tumor lesions delineated by the pathologist and the nuclear medicine physician. The TRE for the co-registration of histopathology and in vivo images was 1.59 mm, while the DICE score related to the site of increased intraprostatic uptake on [⁶⁸Ga]Ga-PSMA and [⁶⁸Ga]Ga-RM2 PET images was 0.54 and 0.75, respectively. This work shows an accurate co-registration method for histopathological and in vivo PET/MRI prostate examinations that allows the quantitative assessment of dual-tracer PET/MRI diagnostic accuracy at a millimetric scale. This approach may unveil radiotracer uptake mechanisms and identify new PET/MRI biomarkers, thus establishing the basis for precision medicine and future analyses, such as radiomics.