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Department of Nuclear Medicine, University Hospital Würzburg, Würzburg
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standard AE monitoring schedule. The secondary objective was to obtain information on the safety and tolerability of vandetanib, which would be compared with data from the pivotal phase III clinical trial [ 20 ]. Assessments Safety was assessed
Department of Clinical Sciences, Lund University, Lund
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Department of Clinical Sciences, Lund University, Lund
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Department of Clinical Sciences, Lund University, Lund
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Department of Clinical Sciences, Lund University, Lund
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18 months. Effects of diclofenac on patient safety and laboratory parameters were registered. Patients Altogether 61 GD patients were included: 30 were randomized to adjuvant treatment with diclofenac and 31 were controls. Basal clinical
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Introduction The Repeated Stable Iodide Prophylaxis in Accidental Situations project (PRIODAC) ( https://en.irsn.fr/research/priodac-project ) was launched by Institute for Radiation Protection and Nuclear Safety in 2014 for a duration of 8
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, 14 ). In this study, we conducted a safety (from the start of procedure up to 30 days postoperatively) and efficacy analysis (up to 24 months of follow-up) of our initial experience in ablating benign TNs (BTN) using a novel MWA system with non
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Center for Head and Neck Surgery, Kusatsu General Hospital, Kusatsu, Japan
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radioiodine-refractory differentiated thyroid cancer [ 9 ]. Lenvatinib also has the possibility of improving disease control and prognosis in ATC [ 10 , 11 ]. However, the efficacy and safety of ATC have not been sufficiently considered. In Japan, lenvatinib
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, 4 , 5 , 6 , 7 , 8 ]. The second step should be directed toward better perioperative assessment of oncologic outcomes and safety [ 1 , 5 , 6 , 7 , 8 , 9 , 10 , 11 ]. The third step would be a determination of the impact of this procedure on functional
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enhances our understanding of the hydrodissection technique and might help improve the safety of time-consuming ablations. Materials and Methods Patients This study was approved by the Review Board of the Third Affiliated Hospital of Sun Yat
Endocrinology Department, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal
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Faculty of Medical Sciences of Lisbon, Lisbon, Portugal
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as first- and second-line TKI therapies. The secondary objective was to describe safety issues associated with these therapeutic agents and their side effect profile. Radiographic and Biochemical Assessment Patients had a radiological
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Department of Nuclear Medicine, The First Hospital of Jilin University, Changchun, China
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Department of Nuclear Medicine & Minnan PET Center, The First Affiliated Hospital of Xiamen University, Xiamen, China
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Human Oncology and Pathogenesis Program, Memorial Sloan-Kettering Cancer Center, New York, New York, USA
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). However, data on salvage therapy using apatinib in this entity are lacking, hampering sufficient exhibition of its efficacy and safety profile in the treatment of RR-DTC. Therefore, we conceived this open-label study based on real-world evidence to
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Unidade de Investigação em Patobiologia Molecular (UIPM), Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal
Nova Medical School: Faculdade de Ciências Médicas da Universidade Nova de Lisboa, Lisbon, Portugal
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Capdevila J Longo F Miller W Jr Chun Bing JT Bonilla CE Chung HC Guren TK Lin CC , Efficacy and safety of pembrolizumab monotherapy in patients with advanced thyroid cancer in the phase 2 KEYNOTE-158 study . Cancer 2023 129 1195 – 1204 . ( https