Hurthle Cell Carcinoma: A 60 Year Experience
Publication Type
Journal Article
Publication Date
2002
Abstract
The aim of this study was to define the clinical behavior and prognostic indicators of outcome in Hürthle cell cancer (HCC). Methods: Diagnosis was confirmed for 56 patients with HCC treated between 1940 and 2000, who form the basis of this study. Primary end points were relapse-free survival (RFS) and disease-specific survival (DSS). Data were analyzed with the Kaplan-Meier method and by log-rank test. Results: The extent of thyroid resection did not predict outcome. Recurrence was a significant predictor of tumor-related mortality. Significant adverse predictors of RFS and DSS were degree of invasion, size >4 cm, extrathyroidal extension, and initial nodal or distant metastases. The most significant predictor of outcome was extent of invasion. Eight-year RFS values for low- and high-risk groups were 100% and 24%. Corresponding rates of 8-year DSS were 100% and 58%. Conclusions: Widely invasive HCC is an aggressive malignancy that identifies patients who are at high risk for recurrence and tumor-related death. Patients with HCC have a prognosis that is reliably predicted by degree of invasion, tumor size, extrathyroidal disease extension, and initial nodal or distant metastasis. Recurrence portends a poor outcome. High-risk patients and those with recurrence should be considered for adjuvant therapy.
Discipline
Econometrics | Medicine and Health Sciences
Research Areas
Econometrics
Publication
Annals of Surgical Oncology
Volume
9
Issue
2
First Page
197
Last Page
203
ISSN
1068-9265
Identifier
10.1007/BF02557374
Publisher
Lippincott, Williams & Wilkins
Citation
Stojadinovic, A.; Hoos, A.; Ghossein, R. A.; Urist, M. J.; Leung, Denis H. Y.; and Spiro, R.H..
Hurthle Cell Carcinoma: A 60 Year Experience. (2002). Annals of Surgical Oncology. 9, (2), 197-203.
Available at: https://ink.library.smu.edu.sg/soe_research/464
Additional URL
https://doi.org/10.1007/BF02557374