医学
核医学
肝细胞癌
剂量学
锥束ct
锥束ct
放射科
计算机断层摄影术
内科学
作者
E. Di Gaeta,Michela Olivieri,Annarita Savi,Patrizia Magnani,Carla Canevari,Simone Gusmini,Diego Palumbo,Giorgia Guazzarotti,Luigi Augello,F. Calabrese,Stephanie Steidler,Federica Cipriani,Margherita Rimini,Andrea Casadei‐Gardini,Luca Aldrighetti,Arturo Chiti,Francesco De Cobelli
标识
DOI:10.1007/s11547-024-01946-0
摘要
Abstract 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 99m Tc-macroaggregated albumin-SPECT/CT ([ 99m Tc]MAA SPECT/CT) to predict and assess the efficacy of TARE based on post-treatment 90 Y 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 90 Y PET/CT considered the standard reference. Treatment simulations for final calculated dose from the different imaging derived volumes were then compared to post-treatment 90 Y PET/CT. Results CBCT resulted as the most accurate method in predicting tumor- (R 2 0.89) and perfused volumes (R 2 0.84). Dosimetry prediction planning performed on derived volumes from the different methods did not show significant difference, yet highest concordance with 90 Y 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.
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