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Targeted Therapy for Advanced Thyroid Cancer: Kinase Inhibitors and Beyond
Author(s) -
Maria E. Cabanillas,
Mabel Ryder,
Camilo Jiménez
Publication year - 2019
Publication title -
endocrine reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.357
H-Index - 272
eISSN - 1945-7189
pISSN - 0163-769X
DOI - 10.1210/er.2019-00007
Subject(s) - lenvatinib , medicine , thyroid cancer , vandetanib , anaplastic thyroid cancer , sorafenib , dabrafenib , cabozantinib , trametinib , cancer , thyroid , medullary thyroid cancer , oncology , targeted therapy , cancer research , kinase , vemurafenib , mapk/erk pathway , metastatic melanoma , hepatocellular carcinoma , biology , microbiology and biotechnology
The treatment of advanced thyroid cancer has undergone rapid evolution in the last decade, with multiple kinase inhibitor drug approvals for each subtype of thyroid cancer and a number of other commercially available drugs that have been studied for this indication. Although most of the US Food and Drug Administration (FDA)–approved drugs are antiangiogenic multikinase inhibitors—vandetanib, cabozantinib, sorafenib, lenvatinib—there are two FDA indications that are mutation specific—dabrafenib/trametinib for BRAF-mutated anaplastic thyroid cancer and larotrectinib for NTRK-fusion thyroid cancer. Furthermore, other mutation-specific drugs, immunotherapies, and novel strategies for advanced thyroid cancer are under investigation. Understanding the molecular basis of thyroid cancer, the drugs of interest for treatment of advanced thyroid cancer, and how these drugs can be administered safely and in the appropriate clinical scenario are the topics of this review.

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