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Management of Progressive Radioiodine-Refractory Thyroid Carcinoma: Current Perspective

Patients with thyroid cancer (TC) usually have an excellent prognosis; however, 5–10% of them develop an advanced disease. The prognosis of this subgroup is still favourable if the lesions respond to radioactive iodine (RAI) treatment. Nearly two-thirds of advanced TC patients become RAI-refractory...

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Autores principales: Nervo, Alice, Retta, Francesca, Ragni, Alberto, Piovesan, Alessandro, Gallo, Marco, Arvat, Emanuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584766/
https://www.ncbi.nlm.nih.gov/pubmed/36275786
http://dx.doi.org/10.2147/CMAR.S340967
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author Nervo, Alice
Retta, Francesca
Ragni, Alberto
Piovesan, Alessandro
Gallo, Marco
Arvat, Emanuela
author_facet Nervo, Alice
Retta, Francesca
Ragni, Alberto
Piovesan, Alessandro
Gallo, Marco
Arvat, Emanuela
author_sort Nervo, Alice
collection PubMed
description Patients with thyroid cancer (TC) usually have an excellent prognosis; however, 5–10% of them develop an advanced disease. The prognosis of this subgroup is still favourable if the lesions respond to radioactive iodine (RAI) treatment. Nearly two-thirds of advanced TC patients become RAI-refractory (RAI-R), and their management is challenging. A multidisciplinary approach in the context of a tumour board is essential to define a personalized strategy. Systemic therapy is not always the best option. In case of slow neoplastic growth and low tumour burden, active surveillance may represent a valuable choice. Local approaches might be considered if the disease progression is limited to a single or few lesions, also in combination and during systemic therapy. Antiresorptive treatment may be started in presence of bone metastases. In case of rapid and/or symptomatic progression involving multiple lesions and/or organs, systemic therapy has to be considered, in absence of contraindications. The multi-kinase inhibitors (MKIs) lenvatinib and sorafenib are currently available as first-line treatment for advanced progressive RAI-R TC. Among second-line options, cabozantinib has been recently approved in RAI-R TC who progressed during MKIs targeting the vascular endothelial growth factor receptor (VEGFR). In the last few years, next-generation sequencing (NGS) assays have been increasingly employed, permitting identification of the genetic alterations harboured by TC, with a significant impact on patients’ management. Novel selective targeted therapies have been introduced for the treatment of RAI-R TC in selected cases: REarranged during Transfection (RET) inhibitors (selpercatinib and pralsetinib) and Tropomyosin Receptor Kinase (TRK) inhibitors (larotrectinib and entrectinib) have recently expanded the panorama of the therapeutic options. Moreover, immune checkpoint inhibitors (ICIs) have shown promising results, and they are still under investigation.
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spelling pubmed-95847662022-10-21 Management of Progressive Radioiodine-Refractory Thyroid Carcinoma: Current Perspective Nervo, Alice Retta, Francesca Ragni, Alberto Piovesan, Alessandro Gallo, Marco Arvat, Emanuela Cancer Manag Res Review Patients with thyroid cancer (TC) usually have an excellent prognosis; however, 5–10% of them develop an advanced disease. The prognosis of this subgroup is still favourable if the lesions respond to radioactive iodine (RAI) treatment. Nearly two-thirds of advanced TC patients become RAI-refractory (RAI-R), and their management is challenging. A multidisciplinary approach in the context of a tumour board is essential to define a personalized strategy. Systemic therapy is not always the best option. In case of slow neoplastic growth and low tumour burden, active surveillance may represent a valuable choice. Local approaches might be considered if the disease progression is limited to a single or few lesions, also in combination and during systemic therapy. Antiresorptive treatment may be started in presence of bone metastases. In case of rapid and/or symptomatic progression involving multiple lesions and/or organs, systemic therapy has to be considered, in absence of contraindications. The multi-kinase inhibitors (MKIs) lenvatinib and sorafenib are currently available as first-line treatment for advanced progressive RAI-R TC. Among second-line options, cabozantinib has been recently approved in RAI-R TC who progressed during MKIs targeting the vascular endothelial growth factor receptor (VEGFR). In the last few years, next-generation sequencing (NGS) assays have been increasingly employed, permitting identification of the genetic alterations harboured by TC, with a significant impact on patients’ management. Novel selective targeted therapies have been introduced for the treatment of RAI-R TC in selected cases: REarranged during Transfection (RET) inhibitors (selpercatinib and pralsetinib) and Tropomyosin Receptor Kinase (TRK) inhibitors (larotrectinib and entrectinib) have recently expanded the panorama of the therapeutic options. Moreover, immune checkpoint inhibitors (ICIs) have shown promising results, and they are still under investigation. Dove 2022-10-21 /pmc/articles/PMC9584766/ /pubmed/36275786 http://dx.doi.org/10.2147/CMAR.S340967 Text en © 2022 Nervo et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Nervo, Alice
Retta, Francesca
Ragni, Alberto
Piovesan, Alessandro
Gallo, Marco
Arvat, Emanuela
Management of Progressive Radioiodine-Refractory Thyroid Carcinoma: Current Perspective
title Management of Progressive Radioiodine-Refractory Thyroid Carcinoma: Current Perspective
title_full Management of Progressive Radioiodine-Refractory Thyroid Carcinoma: Current Perspective
title_fullStr Management of Progressive Radioiodine-Refractory Thyroid Carcinoma: Current Perspective
title_full_unstemmed Management of Progressive Radioiodine-Refractory Thyroid Carcinoma: Current Perspective
title_short Management of Progressive Radioiodine-Refractory Thyroid Carcinoma: Current Perspective
title_sort management of progressive radioiodine-refractory thyroid carcinoma: current perspective
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584766/
https://www.ncbi.nlm.nih.gov/pubmed/36275786
http://dx.doi.org/10.2147/CMAR.S340967
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