Journal of Nuclear Medicine · 2016 · 33 citations · 9 references
PharmacyNuclear MedicinePharmacokineticsHepatic PharmacokineticsPharmacokinetics Of Anticancer AgentsRadiobiologyHepatic ClearanceHepatic Drug DistributionHepatic PerfusionPharmacokinetics In Liver DiseasePharmacokinetics Of Anticancer DrugsDose Distribution To The LiverIntrapulmonary ShuntLiver DosimetryRadioligand PharmacokineticsRadionuclide BiodistributionRadionuclide Uptake QuantificationShunt MeasurementTumor Uptake Kinetics
UNLABELLED: Perfusion scintigraphy using (99m)Tc-labeled albumin aggregates is mandatory before hepatic radioembolization with (90)Y-microspheres. As part of a prospective trial, the intrahepatic and intrapulmonary stability of 2 albumin compounds, (99m)Tc-MAA (macroaggregated serum albumin [MAA]) and (99m)Tc-HSA (human serum albumin [HSA]), was assessed. METHODS: In 24 patients with metastatic colorectal cancer, biodistribution (liver, lung) and liver-lung shunt (LLS) of both tracers (12 patients each) were assessed by sequential planar scintigraphy (1, 5, and 24 h after injection). RESULTS: Liver uptake of both albumin compounds decreased differently. Although initial LLSs at 1 h after injection were similar in both groups, MAA-LLS increased significantly from 1 (3.9%) to 5 h (7.7%) and 24 h (9.9%) after injection, respectively. HSA-LLS did not change significantly (1 to 5 h), indicating a steady state of pulmonary and intrahepatic degradation. CONCLUSION: Compared with (99m)Tc-MAA-microspheres, (99m)Tc-HSA-microspheres are likely more resistant to degradation over time, allowing a reliable LLS determination even at later time points.
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