Vandetanib for the Treatment of Patients With Locally Advanced or Metastatic Hereditary Medullary Thyroid Cancer

J Clin Oncol. 2010 Jan 11;[Epub Ahead of Print], SA Wells Jr, JE Gosnell, RF Gagel, J Mole, D Pfister, JA Sosa, M Skinner, A Krebs, J Vasselli, M Schlumberger

TAKE-HOME MESSAGE

Abstract

SUMMARY

OncologySTAT Editorial Team

Hereditary medullary thyroid cancer (MTC) occurs as 3 distinct inherited syndromes: familial MTC (FMTC), multiple endocrine neoplasia (MEN) type 2A (MEN2A), and MEN type 2B (MEN2B). Early treatment is associated with a 10-year survival rate of 70% to 80%, but 10-year survival rates fall to <50% in patients with distant metastases. Hereditary MTC is caused by germline mutations in the RET proto-oncogene. RET oncoproteins associated with MTC are highly sensitive to agents that inhibit wild-type RET...

NOT A MEMBER?

Registration is FREE

  • Up-to-date oncology news
  • Journal article summaries
  • Commentaries and interviews
  • Drug and interactions database
  • Chemotherapy regimens
  • Daily e-newsletters

 

About Our Journal Scans

View a list of journals that the OncologySTAT editorial team scans every week in order to bring you the most practice-relevant original research and review articles.

Sign up for our newsletters

Too busy to follow cancer's top stories? Sign-up for 1 or more of our free newsletters -- delivered weekly to your inbox.

Cancer Type

  • Bladder
  • Bone
  • Breast
  • Breast (ER-Positive)
  • CNS/Brain
  • Colon and Rectum
  • Endocrine System
  • Esophagus
  • GYN (Non-Ovary)
  • GYN (Ovary)
  • Head and Neck
  • Hodgkin's Lymphoma
  • Kidney (Renal Cell)
  • Leukemia
  • Liver and Bile Duct
  • Lung
  • Multiple Myeloma
  • Myelodysplastic Syndrome
  • Myeloproliferative Diseases
  • Non-Hodgkin's Lymphoma
  • Pancreas
  • Pediatric Cancers
  • Prostate
  • Rare Cancers
  • Skin
  • Soft-Tissue Sarcoma
  • Stomach
  • Testicle
  • Forgot your password?
    Not a member? Free registration