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Medullary Thyroid Carcinoma: Targeted Therapies and Future Directions
Medullary thyroid cancer (MTC) is a rare neuroendocrine neoplasm that accounts for approximately 5% of all thyroid malignancies. The natural history of MTC is characterized by early lymph node and distant metastases, making complete surgical cure often impossible. Conventional chemotherapy and exter...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2798103/ https://www.ncbi.nlm.nih.gov/pubmed/20069043 http://dx.doi.org/10.1155/2009/183031 |
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author | Pinchot, Scott N. Kunnimalaiyaan, Muthusamy Sippel, Rebecca S. Chen, Herbert |
author_facet | Pinchot, Scott N. Kunnimalaiyaan, Muthusamy Sippel, Rebecca S. Chen, Herbert |
author_sort | Pinchot, Scott N. |
collection | PubMed |
description | Medullary thyroid cancer (MTC) is a rare neuroendocrine neoplasm that accounts for approximately 5% of all thyroid malignancies. The natural history of MTC is characterized by early lymph node and distant metastases, making complete surgical cure often impossible. Conventional chemotherapy and external beam radiation have been largely ineffective in altering the natural history of MTC. Therefore, there is a great need to develop novel therapeutic strategies to affect symptom control and reduce tumor burden in patients with widely disseminated disease. Here, we review several pathways which have been shown to be vital in MTC tumorigenesis and focus on the pathways of interest for which targeted drug therapies are currently being developed. |
format | Text |
id | pubmed-2798103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-27981032010-01-12 Medullary Thyroid Carcinoma: Targeted Therapies and Future Directions Pinchot, Scott N. Kunnimalaiyaan, Muthusamy Sippel, Rebecca S. Chen, Herbert J Oncol Review Article Medullary thyroid cancer (MTC) is a rare neuroendocrine neoplasm that accounts for approximately 5% of all thyroid malignancies. The natural history of MTC is characterized by early lymph node and distant metastases, making complete surgical cure often impossible. Conventional chemotherapy and external beam radiation have been largely ineffective in altering the natural history of MTC. Therefore, there is a great need to develop novel therapeutic strategies to affect symptom control and reduce tumor burden in patients with widely disseminated disease. Here, we review several pathways which have been shown to be vital in MTC tumorigenesis and focus on the pathways of interest for which targeted drug therapies are currently being developed. Hindawi Publishing Corporation 2009 2009-12-24 /pmc/articles/PMC2798103/ /pubmed/20069043 http://dx.doi.org/10.1155/2009/183031 Text en Copyright © 2009 Scott N. Pinchot 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 Pinchot, Scott N. Kunnimalaiyaan, Muthusamy Sippel, Rebecca S. Chen, Herbert Medullary Thyroid Carcinoma: Targeted Therapies and Future Directions |
title | Medullary Thyroid Carcinoma: Targeted Therapies and Future Directions |
title_full | Medullary Thyroid Carcinoma: Targeted Therapies and Future Directions |
title_fullStr | Medullary Thyroid Carcinoma: Targeted Therapies and Future Directions |
title_full_unstemmed | Medullary Thyroid Carcinoma: Targeted Therapies and Future Directions |
title_short | Medullary Thyroid Carcinoma: Targeted Therapies and Future Directions |
title_sort | medullary thyroid carcinoma: targeted therapies and future directions |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2798103/ https://www.ncbi.nlm.nih.gov/pubmed/20069043 http://dx.doi.org/10.1155/2009/183031 |
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