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Higher rate of BRAF mutation in papillary thyroid cancer over time†
A single-institution study
Article first published online: 15 MAR 2011
Copyright © 2011 American Cancer Society
Volume 117, Issue 19, pages 4390–4395, 1 October 2011
How to Cite
Mathur, A., Moses, W., Rahbari, R., Khanafshar, E., Duh, Q.-Y., Clark, O. and Kebebew, E. (2011), Higher rate of BRAF mutation in papillary thyroid cancer over time. Cancer, 117: 4390–4395. doi: 10.1002/cncr.26072
All of the authors had full access to all of the data in the study and take full responsibility for the integrity of the data and the accuracy of the data analysis.
- Issue published online: 16 SEP 2011
- Article first published online: 15 MAR 2011
- Manuscript Accepted: 26 JAN 2011
- Manuscript Revised: 18 JAN 2011
- Manuscript Received: 19 OCT 2010
- thyroid cancer;
- somatic mutations;
- molecular changes
The incidence of thyroid cancer has doubled over the past decade. The reason for this dramatic increase in incidence is controversial. Some investigators have suggested that the increased incidence is because of increased detection of small primary tumors as a result of diagnostic scrutiny. Conversely, some investigators have demonstrated an increased incidence across all tumor sizes, suggesting that other factors may play a role. This study was undertaken to investigate the clinical, pathologic, and molecular changes present in papillary thyroid cancer over a 15-year period during which the incidence of papillary thyroid cancer doubled.
A total of 628 patients with conventional papillary thyroid cancer and 228 tumor samples from a single institution were analyzed from 1991 to 2005. Time-trend analyses of demographic, clinical, pathologic, and tumor genotype were performed over three 5-year time periods: group I (1991-1995), group II (1996-2000), and group III (2001-2005).
The authors found no differences in age, sex, ethnicity, primary tumor size, rate of extrathyroidal invasion, or overall TNM cancer stage among the 3 time groups. The rate of BRAF V600E mutation was significantly higher in group III (88% BRAF V600E positive) as compared with groups I and II (51% and 43%, respectively) (P < .001). The rate of all the common somatic mutations was also significantly higher in group III (92% positive) as compared with groups I and II (68% and 64%, respectively) (P < .002).
The rate of BRAF V600E mutation increased significantly over a 15-year period at the authors' institution. The findings suggest that a higher rate of BRAF mutation in papillary thyroid cancer may contribute to the increasing incidence of thyroid cancer. Cancer 2011;. © 2011 American Cancer Society.