PubMed · 1992 · 10 citations · 0 references
MedicineEndocrinologyOncologyEndocrine OncologyNeoplasiaOncologic SurgeryThyroid CancerThyroid DisordersThyroid EndocrinologyThyroid SurgeryThyroid UltrasonographyFollicular Thyroid NeoplasiaFollicular Thyroid NeoplasmsThyroid Adenomas
We report on 492 patients treated for thyroid cancer at the Royal Marsden Hospital between 1932 and 1972: 380 of the patients are now dead. Eighty-three per cent (n = 410) are tumours of follicular cell origin. We found the crude 20-year probability of survival to be 54% in papillary carcinoma, 29% in follicular carcinoma and 1% in anaplastic carcinoma. Considering solely cancer deaths, the survival in papillary cases was 68%. Age, histology (tumour type), extent of primary tumour (T stage), haematogenous metastases (M1 stage) and, to a lesser extent, sex exercised a significant influence on survival. We support the use of these five factors to produce a prognostic index for estimating the level of risk for tumours of follicular cell origin. We add our experience in the non-follicular cell tumours of medullary carcinoma (3%), lymphoma (7%) and fibrosarcoma (1%).