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Radioprotection après injection thérapeutique de [131I]-mIBG : données préalables à l’ouverture du protocole MIITOP-0607
Authors:G Petyt  O Cougnenc  A-S Defachelles  J-L Cazin  P Carpentier
Institution:1. Molecular Radiopharmacy, INRASTES, National Center for Scientific Research “Demokritos”, GR-153 10 Athens, Greece;2. Department of Nuclear Medicine, Erasmus MC, 3015 CE Rotterdam, The Netherlands;3. Department of Radiology, Erasmus MC, 3015 CE Rotterdam, The Netherlands;1. Research Center for Translational Medicine, East Hospital, Tongji University School of Medicine, Shanghai 200120, People''s Republic of China;2. Department of Preventive Medicine, Tongji University School of Medicine, East Hospital, Shanghai 200120, People''s Republic of China;3. Department of Anesthesiology, East Hospital, Tongji University School of Medicine, 150 Jimo Road, Shanghai 200120, People''s Republic of China;4. Department of Hospital Infections, Shanghai Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, People''s Republic of China;5. Department of Anesthesiology, The Eye, Ear, Nose, and Throat Hospital, Fudan University, Shanghai 200031, People''s Republic of China
Abstract:IntroductionThe MIITOP-0607 protocol, studying the efficiency of administration of topotecan and myelosupressive 131I]-mIBG therapy in children affected by neuroblastoma, needed to assess irradiation risks on staff and family of children to obtain the agreement of the Autorité de sûreté nucléaire (ASN). Our aim was to quantify irradiation of the staff during preparation of the mIBG and to assay the irradiation and contamination of the accompanying persons.Patient and methodsRadiation exposure of the staff was measured during the preparation, transport and administration of the first treatment. Salivary and urinary excretions were monitored well as the atmospheric radioactivity. Radiation exposure and contamination of the accompanying persons were also measured.ResultsFinger dose of 3 mSv and whole body dose of 50 μSv were estimated for preparation of an 11.1 GBq syringe. Irradiation from urinary activity can be as low as 100 μSv if a dedicated device is used. Salivary excretion decreased rapidly during the first 24 hours. Atmospheric contamination always remained below 25 Bq m?3. Total irradiation of the accompanying persons is about 2.35 mSv for the two consecutive injections (9,3 and 11,1 GBq). Internal contamination occurred only once and corresponded to a 27 μSv whole body irradiation and 670 μSv thyroid irradiation.ConclusionThis study shows the safety of 131I]-mIBG treatments using high activities. The involved dose is not negligible but seems to be acceptable in the specific paediatric oncology context if radioprotection instructions are met and if optimization of protocols is performed.
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