Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy
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Department of Biotechnology and Translational Medicine, University of Milan, Milan, Italy
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Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy
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previous study ( 16 ) are included in the present series. Thirty-one out of 36 patients were MKIs-naive, and 5 out of 36 were on second-line treatment, as patients on SELP were previously treated with VAN. The clinical–pathological features and treatment
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become refractory to RAI therapy ( 2 ). The prognosis for these patients is poor, and the 10-year survival rate for RAI-refractory (RAI-R) thyroid cancer is 10% ( 3 ). Multi-kinase inhibitors (MKIs) are the standard of care for RAI-R DTC. While MKIs are
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Food and Drug Administration (FDA) approved the use of several multikinase inhibitors (MKIs) based on recent clinical trials showing their ability to limit disease progression [ 6 , 7 , 8 , 9 , 10 , 11 ]. It is not known, however, whether the
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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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progress in the treatment of advanced thyroid carcinomas has occurred in the past years with the development of multikinase inhibitors (MKIs) ( 1 , 2 , 3 ). The Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have approved the
Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy
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years, many new drugs have been investigated for the treatment of progressive RAI-R TC. Currently, 2 multikinase inhibitors (MKI) have been approved for treatment by the Food and Drug Administration (FDA) and the European Medicines Agency (EMA), e
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Introduction Thanks to the results of DECISION and SELECT trials, sorafenib and lenvatinib are the only MKIs approved by both the U.S. Food and Drug Administration (FDA) and the European Medical Agency (EMA) for the first-line treatment of
Endocrine Tumour Center at West German Cancer Center, Member of ENDO-ERN and EURACAN, University Hospital Essen, University of Duisburg-Essen, Essen, Germany
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Endocrine Tumour Center at West German Cancer Center, Member of ENDO-ERN and EURACAN, University Hospital Essen, University of Duisburg-Essen, Essen, Germany
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University Duisburg-Essen, Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany
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University Duisburg-Essen, Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany
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Endocrine Tumour Center at West German Cancer Center, Member of ENDO-ERN and EURACAN, University Hospital Essen, University of Duisburg-Essen, Essen, Germany
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PAX8 staining showed a nuclear expression pattern. Scale bar, 100 µm. Fig. 3. Representative neck CT scans showing response of the PSCC of the thyroid to combined MKI treatment (baseline, a ) at 3 ( b ) and 6 ( c ) months and regrowth
Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy
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Department of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy
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Department of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy
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Department of Biotechnology and Translational Medicine, University of Milan, Milan, Italy
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Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy
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Introduction Multikinase inhibitors (MKIs) with strong anti-angiogenetic action are frequently used for the treatment of advanced radioiodine-refractory differentiated thyroid cancer (RAI-R DTC) or medullary thyroid cancers (MTCs) ( 1 , 2
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MTC for whom treatment with systemic therapy is planned ( 12 ). Systemic therapies in advanced or metastatic MTC (aMTC) include multikinase inhibitors (MKIs) and selective RET inhibitors ( 12 , 13 ). ESMO treatment guidelines from April 2022
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advanced/metastatic ( 1 ). According to European Medicines Agency (EMA) indications, two multikinase inhibitors (MKIs) (i.e. vandetanib and cabozantinib) and one highly selective RET inhibitor (i.e. selpercatinib) have been approved for the treatment of