Research Article

Whether Detection of Gene Mutations Could Identify Low- or High-Risk Papillary Thyroid Microcarcinoma? Data from 393 Cases Using the Next-Generation Sequencing

Table 7

Multinomial logistic regression analysis to evaluate the association between the presence of BRAFV600E and patient characteristics of PTMC.

Independent variableORCI 95%

Gender
 F1Ref.
 M1.490.66–3.370.324
Age at diagnosis (years)
 ≤400.460.07–3.000.455
 (40, 60]0.240.04–1.460.089
 >601Ref.
Maximum tumor size (mm)
 ≤51Ref.
 >54.922.40-10.07<0.001
Chronic lymphocytic thyroiditis
 No1Ref.
 Yes0.70.31–1.600.401
Bilateralism
 No1Ref.
 Yes0.60.19–1.900.686
Multifocality
 No1Ref.
 Yes5.121.48-17.700.996
Intrathyroid spread
 No1Ref.
 Yes1.020.10-10.250.67
Extrathyroidal extension
 No1Ref.
 Yes2.390.73–7.780.749
Lymph node metastases
 No1Ref.
 Central compartment2.530.78–8.210.481
 Laterocervical compartment80.65–98.990.627
 Central +2.90.54-15.570.985
 Laterocervical compartment
  ≤51Ref.
  >50.850.23–3.090.625
Staging (VIII ed. TNM)
 I1Ref.
 II3.680.54-25.150.256
Tumor recurrence
 Yes0.660.51–8.600.877
 No1Ref.
 n.a.0.030.00–0.590.048

na: not available and PTMC: papillary thyroid microcarcinoma. Significant differences are shown in bold characters .