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Radionuclide selection and model absorbed dose calculations for radiolabeled tumor associated antibodies
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1984
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EngineeringPathologyRadionuclide SelectionTheranosticsRadiopharmaceutical TherapyTumor LocalizationRadiation Therapy PlanningRadiation OncologyTumor LocationNuclear MedicineRadiolabeled TumorCancer ResearchRadiologyAdaptive RadiotherapyRadiation TherapyMedicineRadionuclide TherapyHalf-life DataDosimetryTumor MicroenvironmentRadiopharmaceuticalsOncologyDose Calculations
Nuclides were selected based on physical properties that make them suitable for imaging or therapeutic antibody labeling. The study compiled half‑life, specific activity, and organ dose data for nine radionuclides and adopted biodistribution estimates for antibody uptake and clearance to model absorbed doses. Absorbed‑dose calculations showed that Re‑186 and Y‑90 are the most promising therapeutic radiolabels, offering long half‑lives, minimal gamma emission, suitable beta energy, stable daughters, and good chelate compatibility.
An absorbed dose calculation comparison has been computed for radiolabeled tumor associated antibodies distributed over a standard geometry and tumor location. Half-life data, maximum specific activities, and relative organ doses of nine radionuclides, Cu-67, Br-77, Br-82, Y-90, Tc-99m, In-111, I-131, Re-186, and At-211, have been compiled in which the radionuclides were assumed to be coupled with antibody. These nuclides were chosen on the basis of physical characteristics that warranted their inclusion as either imaging or therapy radiolabels. Radionuclide biodistribution data based on current available estimates for antibody uptake and clearance in humans has been adopted. Re-186 and Y-90 have been determined to be among the best therapy radiolabels since they possess sufficiently long half lives necessary for tumor localization, little or no gamma radiation, intermediate beta energy, stable daughter products, and have a reasonable chance to form a stable chelate with an antibody system.