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Challenges Associated with Tyrosine Kinase Inhibitor Therapy for Metastatic Thyroid Cancer

Tyrosine kinase inhibitors (TKIs) which target angiogenesis are promising treatments for patients with metastatic medullary and differentiated thyroid cancers. Sorafenib, sunitinib, and pazopanib are commercially available drugs which have been studied in these diseases. Vandetanib is the first drug...

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Autores principales: Cabanillas, Maria E., Hu, Mimi I., Durand, Jean-Bernard, Busaidy, Naifa L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189619/
https://www.ncbi.nlm.nih.gov/pubmed/22007339
http://dx.doi.org/10.4061/2011/985780
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author Cabanillas, Maria E.
Hu, Mimi I.
Durand, Jean-Bernard
Busaidy, Naifa L.
author_facet Cabanillas, Maria E.
Hu, Mimi I.
Durand, Jean-Bernard
Busaidy, Naifa L.
author_sort Cabanillas, Maria E.
collection PubMed
description Tyrosine kinase inhibitors (TKIs) which target angiogenesis are promising treatments for patients with metastatic medullary and differentiated thyroid cancers. Sorafenib, sunitinib, and pazopanib are commercially available drugs which have been studied in these diseases. Vandetanib is the first drug approved in the United States for treatment of medullary thyroid cancer. These TKIs are used as chronic therapies, and therefore it is imperative to understand the adverse event profile in order to avoid excessive toxicity and maintain patients on therapy as long as it proves beneficial. Here we review common toxicities, management of these, and other challenging situations that arise when using TKIs in patients with thyroid cancer.
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spelling pubmed-31896192011-10-17 Challenges Associated with Tyrosine Kinase Inhibitor Therapy for Metastatic Thyroid Cancer Cabanillas, Maria E. Hu, Mimi I. Durand, Jean-Bernard Busaidy, Naifa L. J Thyroid Res Review Article Tyrosine kinase inhibitors (TKIs) which target angiogenesis are promising treatments for patients with metastatic medullary and differentiated thyroid cancers. Sorafenib, sunitinib, and pazopanib are commercially available drugs which have been studied in these diseases. Vandetanib is the first drug approved in the United States for treatment of medullary thyroid cancer. These TKIs are used as chronic therapies, and therefore it is imperative to understand the adverse event profile in order to avoid excessive toxicity and maintain patients on therapy as long as it proves beneficial. Here we review common toxicities, management of these, and other challenging situations that arise when using TKIs in patients with thyroid cancer. SAGE-Hindawi Access to Research 2011 2011-10-04 /pmc/articles/PMC3189619/ /pubmed/22007339 http://dx.doi.org/10.4061/2011/985780 Text en Copyright © 2011 Maria E. Cabanillas et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Cabanillas, Maria E.
Hu, Mimi I.
Durand, Jean-Bernard
Busaidy, Naifa L.
Challenges Associated with Tyrosine Kinase Inhibitor Therapy for Metastatic Thyroid Cancer
title Challenges Associated with Tyrosine Kinase Inhibitor Therapy for Metastatic Thyroid Cancer
title_full Challenges Associated with Tyrosine Kinase Inhibitor Therapy for Metastatic Thyroid Cancer
title_fullStr Challenges Associated with Tyrosine Kinase Inhibitor Therapy for Metastatic Thyroid Cancer
title_full_unstemmed Challenges Associated with Tyrosine Kinase Inhibitor Therapy for Metastatic Thyroid Cancer
title_short Challenges Associated with Tyrosine Kinase Inhibitor Therapy for Metastatic Thyroid Cancer
title_sort challenges associated with tyrosine kinase inhibitor therapy for metastatic thyroid cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189619/
https://www.ncbi.nlm.nih.gov/pubmed/22007339
http://dx.doi.org/10.4061/2011/985780
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