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      18 Anniversary Conference 20 Years Cyprus Society Of Nuclear Medicine (CYSNM20) Limassol Cyprus, 6 th– 10 th November 2019

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      World Journal of Nuclear Medicine
      Wolters Kluwer - Medknow

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          Abstract

          Objectives: The aim of the study is to provide the first pre- and peri-dosimetry analyses of 177Lu-DOTATATE patients with neuroendocrine tumors receiving higher activities compared to the standard 177Lu-DOTATATE treatment and to compare the results of three different computer codes used for calculating the absorbed dose to the kidneys. In addition, the blood-based and image-based techniques were applied to estimate bone marrow absorbed doses were analyzed to find an optimal way to estimate bone marrow absorbed doses. Methods: Multiple blood samples (up to 96 h), 24 h SPECT/CT data and a series of WB planar images (up to 95 h) were acquired after an administered therapy activity of 14.4 - 19.3 GBq. The administered activities were chosen based on pre-dosimetry kidney absorbed dose coefficients obtained without kidney protection with the aim not to exceed a kidney absorbed dose of 23 Gy after a single administration of 177Lu-DOTATATE (170-237 MBq). Time-activity curves (TAC) and the corresponding time-integrated activity coefficients (TIACs) for kidneys, blood, whole-body and lumbar vertebrae 2-4 (representing bone marrow) were calculated. Based on these data, patient-specific kidney absorbed dose coefficients were obtained with NUKDOS, OLINDA1.1 and IDAC-Dose 2.1. Absorbed doses to the blood were calculated as described by Eberlein et al.[1] Image-based and blood-based bone marrow absorbed doses were analyzed and compared. Results: In blood we observed lower than 8% of the injected activity 2 h after injection (assuming a blood volume of 5.3 liter). Compared to the standard therapy (7.4 GBq) the absorbed dose to the blood after 48 h is higher (mean: 186±54 mGy vs. 79±16 mGy (1)). Image-based (NUKDOS) and blood-based bone marrow absorbed doses ranged from 0.3-0.8 Gy (LV2-4-based) and 0.1-0.3 Gy (blood-based), respectively. After injection of 14.4 - 19.3 GBq 177Lu-DOTATATE, patient-specific kidney absorbed dose coefficients and doses were identical for NUKDOS, OLINDA 1.1 and IDAC-Dose 2.1 and well below 23 Gy (Pat 1: 0.7 Gy/GBq, 9.6 Gy; Pat 2: 0.3 Gy/GBq, 4.8 Gy; Pat 3: 0.4 Gy/GBq, 7.0 Gy). Conclusions: This study provides the first pre- and peri-therapeutic dosimetry data of 177Lu-DOTATATE patients receiving patient-specific higher activities compared to the standard 177Lu-DOTATATE treatment. The results of this study show that high 177Lu-DOTATATE activities can be administered safely based on pre-therapeutic kidney dosimetry. In addition, blood-based bone marrow absorbed doses are by a factor of three lower compared to image-based bone marrow absorbed doses advocating the use of image-based dosimetry. When patient-specific kidney masses are used, OLINDA 1.1 and IDAC-Dose 2.1 provide similar results with NUKDOS which uses patient-specific voxel-based S-values.

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          DNA damage in blood lymphocytes in patients after 177Lu peptide receptor radionuclide therapy

          Purpose The aim of the study was to investigate DNA double strand break (DSB) formation and its correlation with the absorbed dose to the blood lymphocytes of patients undergoing their first peptide receptor radionuclide therapy (PRRT) with 177Lu-labelled DOTATATE/DOTATOC. Methods The study group comprised 16 patients receiving their first PRRT. At least six peripheral blood samples were obtained before, and between 0.5 h and 48 h after radionuclide administration. From the time–activity curves of the blood and the whole body, residence times for blood self-irradiation and whole-body irradiation were determined. Peripheral blood lymphocytes were isolated, fixed with ethanol and subjected to immunofluorescence staining for colocalizing γ-H2AX/53BP1 DSB-marking foci. The average number of DSB foci per cell per patient sample was determined as a function of the absorbed dose to the blood and compared with an in vitro calibration curve established in our laboratory with 131I and 177Lu. Results The average number of radiation-induced foci (RIF) per cell increased over the first 5 h after radionuclide administration and decreased thereafter. A linear fit from 0 to 5 h as a function of the absorbed dose to the blood agreed with our in vitro calibration curve. At later time-points the number of RIF decreased, indicating progression of DNA repair. Conclusion Measurements of RIF and the absorbed dose to the blood after systemic administration of 177Lu may be used to obtain data on the individual dose–response relationships in vivo. Individual patient data were characterized by a linear dose-dependent increase and an exponential decay function describing repair. Electronic supplementary material The online version of this article (doi:10.1007/s00259-015-3083-9) contains supplementary material, which is available to authorized users.
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            In Vitro Model System for Biological Quality Control and Functional Research of Radiopharmaceuticals used for Targeted Radionuclide Therapy

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              Author and article information

              Journal
              World J Nucl Med
              World J Nucl Med
              WJNM
              World Journal of Nuclear Medicine
              Wolters Kluwer - Medknow (India )
              1450-1147
              1607-3312
              October 2019
              22 October 2019
              : 18
              : Suppl 1
              : S1-S17
              Affiliations
              [1 ]Department of Nuclear Medicine, Würzburg, Germany
              [2 ]Gastrology, University of Würzburg, Würzburg, Germany
              [1 ]PHI University institution of positron emission tomography in North Macedonia
              [1 ]Molecular Radiopharmacy, INRASTES, NCSR “Demokritos,” Athens, Greece
              [2 ]Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands
              [3 ]Cyclotron Rotterdam BV, Erasmus MC, Rotterdam, The Netherlands
              [1 ]Molecular Radiopharmacy, INRASTES, NCSR “Demokritos,” Athens, Greece
              [2 ]Cyclotron Rotterdam BV, Erasmus MC, Rotterdam, The Netherlands
              [1 ]Department of Biophysics and Physical Chemistry, Charles University, Hradec Kralove, Czech Republic
              [2 ]Department of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Kralove, Charles University, Hradec Kralove, Czech Republic
              [3 ]Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic
              [1 ]Department of Academic Nuclear Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece
              [2 ]Lab of Medical Physics, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece
              [1 ]Nuclear Medicine Laboratory, Emergency Clinical County Hospital “St. Spiridon,”, Iasi, Romania
              [2 ]Faculty of Medicine, University “Grigore T. Popa,”, Iasi, Romania
              [3 ]Department of Radiology, Emergency Clinical County Hospital “St. Spiridon,”, Iasi, Romania
              [4 ]Department of Obstetrics and Gynecology, Obstetrics and Gynecology Hospital “Cuza Voda,”, Iasi, Romania
              [1 ]Clinical Department of Nuclear Medicine, Riga East University Hospital, Riga, Latvia
              [2 ]The Latvian Maritime Medical Centre, Riga, Latvia
              [3 ]Kodolmedicinas Klinika Ltd, Riga, Latvia
              [4 ]Institute of Biomedical Engineering and Nanomedicine, Riga Technical University, Riga, Latvia
              [5 ]Arbor Medical Corporation Ltd, Riga, Latvia
              [6 ]Faculty of Biology, University of Latvia, Riga, Latvia
              [7 ]Faculty of Chemistry, University of Latvia, Riga, Latvia
              [1 ]Laboratory of Molecular Genetics, Institute of Oncology, Riga Stradins University, Riga, Latvia
              [2 ]Clinical Department of Nuclear Medicine, Riga East University Hospital, Riga, Latvia
              [3 ]Kodolmedicinas Klinika Ltd, Riga, Latvia
              [4 ]Institute of Chemical Physics, University of Latvia, Riga, Latvia
              [5 ]Institute of Microbiology and Biotechnology, University of Latvia, Riga, Latvia
              [6 ]Arbor Medical Corporation Ltd, Riga, Latvia
              [1 ]Kodolmedicinas Klinika Ltd, Riga, Latvia
              [2 ]Institute of Biomedical Engineering and Nanomedicine, Riga Technical University, Riga, Latvia
              [3 ]Clinical Department of Nuclear Medicine, Riga East University Hospital, Riga, Latvia
              [4 ]Institute of Food Safety, Animal Health and Environment “BIOR”, Riga, Latvia
              [5 ]Institute of Polymer Materials, Faculty of Materials Science and Applied Chemistry, Riga Technical University, Riga, Latvia
              [6 ]Institute of Chemical Physics, University of Latvia, Riga, Latvia
              [1 ]Kodolmedicinas Klinika Ltd, Riga, Latvia
              [2 ]Institute of Biomedical Engineering and Nanomedicine, Riga Technical University, Riga, Latvia
              [3 ]Clinical Department of Nuclear Medicine, Riga East University Hospital, Riga, Latvia
              [4 ]Institute of Chemical Physics, University of Latvia, Riga, Latvia
              [1 ]Nuclear Medicine Laboratory, Emergency County Hospital “Sf. Spiridon,”, Iasi, Romania
              [2 ]University of Medicine and Pharmacy “Grigore T. Popa,”, Iasi, Romania
              [3 ]Department of Cardiology, Emergency County Hospital “Sf. Spiridon,”, Iasi, Romania
              [4 ]Institute of Cardiovascular Disease, Clinical Hospital “Dr. C. I. Parhon,”, Iasi, Romania
              [1 ]Department of Biophysics and Medical Physics, “Grigore T. Popa” University of Medicine and Pharmacy, Kragujevac, Serbia
              [2 ]Nuclear Medicine Laboratory, “St. Spiridon” Emergency County Hospital, Kragujevac, Serbia
              [5 ]Endocrinology Clinic, “St. Spiridon” Emergency County Hospital, Iasi, Romania, Kragujevac, Serbia
              [3 ]Center for Nuclear Medicine, Clinical Center Kragujevac, Kragujevac, Serbia
              [4 ]Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia
              [1 ]Nuclear Medicine Center in Clinica Modelo, Parana, Entre Ríos, Argentine
              [1 ]Academic Nuclear Medicine Department of Aristotle University of Thessaloniki, Thessaloniki, Greece
              [2 ]Nuclear Medicine Department of Theagenio Cancer Hospital, Thessaloniki, Greece
              [3 ]Department of Endocrinology, Theageneio Cancer Center, Thessaloniki, Greece
              [1 ]Aghia Sofia' Children's Hospital of Greece - Elpida Oncology Unit, Athens, Greece
              [1 ]Department of Nuclear Medicine, Umhlanga Molecular Imaging and Therapy Centre, Netcare Umhlanga Hospital, Umhlanga, South Africa
              [1 ]Department of Nuclear Medicine, Theageneio Cancer Center, Thessaloniki, Greece
              [1 ]Dr. Saul Hertz Archives
              [1 ]3 rd Academic Nuclear Medicine Department of Aristotle University of Thessaloniki, Papageorgiou Hospital, Thessaloniki, Greece
              [2 ]Nuclear Medicine department of “Theagenio” Cancer Hospital of Thessaloniki, Thessaloniki, Greece
              [3 ]Department of Endocrinology, Theageneio Cancer Center, Thessaloniki, Greece
              [1 ]Department of Nuclear Medicine, Theageneio Cancer Center, Thessaloniki, Greece
              [1 ]Academic Nuclear Medicine Department of Aristotle University of Thessaloniki, Greece
              [2 ]Nuclear Medicine Department of Theagenio Cancer Center of Thessaloniki, Greece
              [3 ]Faculty of Medicine Comenius University, Bratislava, Slovakia
              [1 ]Academic Nuclear Medicine Department of Aristotle University of Thessaloniki, Greece
              [1 ]Academic Nuclear Medicine Department of Aristotle University of Thessaloniki, Greece
              [1 ]Academic Nuclear Medicine Department of Aristotle University of Thessaloniki, Greece
              [1 ]Central University Emergency Military Hospital, Bucharest, Romania
              Article
              WJNM-18-1
              6854878
              de38726a-e390-43ca-9886-4ce0b635209e
              Copyright: © 2019 World Journal of Nuclear Medicine

              This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

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