HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Management of microcarcinomas (papillary and medullary) of the thyroid.

AbstractPURPOSE OF REVIEW:
Microcarcinomas of the thyroid gland are defined by the size criteria as tumors measuring less than 1 cm in greatest dimension. The clinical significance of papillary thyroid microcarcinoma (PTMC) and medullary thyroid microcarcinoma (MTMC) is debatable. Variation in practice patterns exist in the United States with regard to diagnosis, treatment, and long-term management. We review the most recent guidelines on the management of these controversial malignancies.
RECENT FINDINGS:
PTMC has recently been shown to be the most common thyroid malignancy in patients older than 45 years in the United States. The management of patients with PTMC is not well defined, although recent studies have indicated that total or near-total thyroidectomy decreases overall recurrence rate. BRAF mutation testing plays an increasingly important role in perioperative management and has potential for targeted molecular therapies.Prophylactic thyroidectomy is indicated early in life for RET mutation carriers at risk for medullary thyroid cancer. New evidence suggests that timing may be personalized based on specific exon mutations and serum calcitonin levels. The biological significance and surgical management of MTMC have been debated, but the most recent studies indicate a relatively high incidence of lymph node metastases, distant metastases, and persistently elevated postoperative calcitonin; and argue for the aggressive management of even the smallest MTMCs.
SUMMARY:
Total or near-total thyroidectomy is the treatment of choice in patients with PTMC in order to eradicate multifocal disease and decrease overall recurrence rate. If there are palpable, biopsy-proven, or grossly apparent metastases at the time of operation, central lymphadenectomy should be performed. Prophylactic thyroidectomy in hereditary cases of MTMC may be guided by knowledge of specific exon mutations and calcitonin levels. The extent of operation for both hereditary and sporadic MTMC is nonstandardized, and further studies are needed to clarify this issue.
AuthorsLeslie S Wu, Stacey A Milan
JournalCurrent opinion in oncology (Curr Opin Oncol) Vol. 25 Issue 1 Pg. 27-32 (Jan 2013) ISSN: 1531-703X [Electronic] United States
PMID23042124 (Publication Type: Journal Article, Review)
Chemical References
  • Antineoplastic Agents
  • Biomarkers, Tumor
  • Genetic Markers
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins B-raf
Topics
  • Antineoplastic Agents (therapeutic use)
  • Biomarkers, Tumor (genetics)
  • Carcinoma, Medullary (diagnosis, genetics, therapy)
  • Carcinoma, Papillary (diagnosis, genetics, therapy)
  • Catheter Ablation (methods)
  • Genetic Markers
  • Humans
  • Practice Guidelines as Topic
  • Protein Kinase Inhibitors (therapeutic use)
  • Proto-Oncogene Proteins B-raf (genetics)
  • Radioimmunotherapy
  • Thyroid Neoplasms (diagnosis, genetics, therapy)
  • Thyroidectomy (methods)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: