Table 1.
Characteristic | n (%)a |
---|---|
Age, years | |
Median | 67 |
Range | 50–83 |
Sex | |
Male | 6 (86) |
Female | 1 (14) |
Tumor histology | |
Classical variant papillary thyroid cancer | 2 (29) |
Tall cell variant papillary thyroid cancer | 2 (29) |
Poorly differentiated thyroid cancerb | 3 (42) |
Tumor genotype | |
BRAFV600E mutation | 7 (100) |
Prior treatments of 131I per patient | |
0 | 1 (14) |
1 | 6 (86) |
Other prior treatments for thyroid cancer | |
Doxorubicin (concurrently with RT) | 2 (29) |
VEGFR-targeted TKI | 0 (0) |
Sites of disease | |
Local (thyroid bed, neck nodes or mediastinal extension/nodes) | 7 (100) |
Lungs | 6 (86) |
Distant nodes (hilar, paraaortic, subcarinal) | 2 (29) |
Soft tissue nodules | 1 (14) |
Bone | 1 (14) |
Values are given as number of patients (%) unless otherwise specified; percentages are calculated based on the total number of patients enrolled (n = 7).
Poorly differentiated thyroid carcinoma was defined by mitoses and tumor necrosis (11).
I, radioactive iodine; RT, radiation therapy; TKI, tyrosine kinase inhibitor; VEGFR, vascular endothelial growth factor receptor.