Prognosis and treatment effectiveness of medullary thyroid carcinoma (MTC)
are largely related to the tumour stage, so that early diagnosis represents
an important goal for the management of patients. Recent advances in genet
ic testing have improved the clinical approach to the familial MTC syndrome
s. There is general agreement that the primary operation for MTC should obt
ain the complete removal of the neoplastic tissue in the neck, because any
adjuvant treatment has never been proven to be effective. The management of
residual/recurrent or metastatic MTC still remains controversial, although
a multimodal approach to advanced disease may be of value in palliation or
local control of tumour progression. The role of surgery, external radioth
erapy, radionuclide therapy and medical treatment, including biological res
ponse modifiers and cytotoxic drugs, are reviewed and discussed.