Medullary thyroid carcinoma: a narrative historical review.


Journal

Expert review of anticancer therapy
ISSN: 1744-8328
Titre abrégé: Expert Rev Anticancer Ther
Pays: England
ID NLM: 101123358

Informations de publication

Date de publication:
08 2022
Historique:
pubmed: 14 6 2022
medline: 6 8 2022
entrez: 13 6 2022
Statut: ppublish

Résumé

Sporadic or hereditary medullary thyroid carcinoma (MTC) is an uncommon thyroid malignancy arising from calcitonin secreting parafollicular C cells. Interestingly, MTC and calcitonin were distinct entities that were discovered independently yet concurrently, and their association was unknown. This review aims to present a historical review of the evolution of our understanding of MTC and its tumor marker calcitonin to highlight the prominent individuals that influenced and shaped our knowledge of this uncommon thyroid cancer type up to the dawn of the 21 Surgery remains the cornerstone of treatment for localized MTC. However, several new treatment options are either available or in development for advanced or metastatic MTC, including several novel small molecules targeting oncogenic

Identifiants

pubmed: 35694971
doi: 10.1080/14737140.2022.2089118
doi:

Substances chimiques

Calcitonin 9007-12-9
Proto-Oncogene Proteins c-ret EC 2.7.10.1

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

823-834

Auteurs

Amanda Wong (A)

Department of Surgery, St. Paul's Hospital & University of British Columbia, Vancouver, British Columbia, Canada.

Kylie Nabata (K)

Department of Surgery, St. Paul's Hospital & University of British Columbia, Vancouver, British Columbia, Canada.

Sam M Wiseman (SM)

Department of Surgery, St. Paul's Hospital & University of British Columbia, Vancouver, British Columbia, Canada.

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Classifications MeSH