2019 AAPM Annual Meeting
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Session Title: Dosimetry in Radionuclide Therapy
Question 1: Radiopharmaceutical therapy dosimetry consists of:
Reference:Loevinger R, Budinger TF, Watson EE. MIRD Primer for Absorbed Dose Calculation. New York Society of Nuclear Medicine, 1988.
Choice A:Calculation of whole organ absorbed dose for prospective treatment planning and constraints on normal organ toxicity
Choice B:Calculation of tumor absorbed dose for retrospective dose-response studies
Choice C:Use of radiobiological, pharmacokinetic and small scale anatomical modeling
Choice D:All of the above
Question 2: Challenges in Targeted Alpha-particle therapy dosimetry include:
Reference:Sgouros G, Roeske JC, McDevitt MR, Palm S, Allen BJ, Fisher DR, Brill AB, Song H, Howell RW, Akabani G. MIRD Pamphlet No. 22 (Abridged): Radiobiology and Dosimetry of -Particle Emitters for Targeted Radionuclide Therapy. J Nucl Med 2010;51(2):311 328
Choice A:Low count rate for SPECT or PET imaging
Choice B:Short range of decay and micro-localization requiring small scale modeling
Choice C:Re-localization of radioactive daughter particles in the body
Choice D:Poorly known or documented radiobiological parameters
Choice E:All of the above
Question 3: The OLINDA/EXM software is now distributed by:
Reference:Huizing et al. Dosimetry methods and clinical applications in peptide receptor radionuclide therapy for neuroendocrine tumours: a literature review EJNMMI Research (2018) 8:89
Choice A:Varian Medical Systems
Choice B:Hermes Medical Solutions
Choice C:Dosisoft
Choice D:MIM Software Inc.
Question 4: Commercial voxel-level dosimetry software is primarily being used to:
Reference:Kafrouni et al. Retrospective voxel-based dosimetry for assessing the body surface area model ability to predict delivered dose and radioembolization outcome J Nucl Med. (2018) 59(8):1289-1295
Choice A:Verify dose distributions from selective internal radiation therapy
Choice B:Perform treatment planning calculations for selective internal radiation therapy
Choice C:Verify dose distributions from systemically delivered RPT agents (e.g. Lutathera®)
Choice D:Perform treatment planning calculations for systemically delivered RPT agents (e.g. Lutathera®)
Question 5: Which of the following is the major contributor to self absorbed dose in therapies involving Lu-177 or Y-90?
Reference:Sandström M, Garske-Román U, Johansson S, Granberg D, Sundin A, Freedman N. Kidney dosimetry during (177)Lu-DOTATATE therapy in patients with neuroendocrine tumors: aspects on calculation and tolerance. Acta Oncol. 2018 Apr;57(4):516-521.
Choice A:Bremsstrahlung photons
Choice B:Gamma-rays
Choice C:Beta-particles
Choice D:Both gamma-rays and beta particles contribute equally
Question 6: Source region time-integrated activity for post-therapy imaging based absorbed dose estimation in Y-90 microsphere radioembolization typically
Reference:Elschot M, Vermolen BJ, Lam MG, de Keizer B, van den Bosch MA, de Jong HW. Quantitative comparison of PET and Bremsstrahlung SPECT for imaging the in vivo yttrium-90 microsphere distribution after liver radioembolization. PLoS One. 2013;8(2):e55742.
Choice A:requires Y-90 imaging at multiple time points
Choice B:requires Y-90 imaging at a single time point
Choice C:can be obtained by PET imaging only
Choice D:cannot be determined as Y-90 has no associated gamma-rays
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