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Updated: Sep 12, 2025

Spontaneous Murine Model of Anaplastic Thyroid Cancer
Published on: February 3, 2023
Clinical Risk Factor for Detected Distant Metastasis and Anaplastic Transformation After Reoperation in
Min-Su Kim1, Yung Jee Kang2, Soon-Hyun Ahn2
1Department of Otorhinolaryngology-Head and Neck Surgery CHA Bundang Medical Center, CHA University School of Medicine Seongnam Republic of Korea.
Objectives:
Research on detected distant metastasis or anaplastic transformation in recurrent/persistent differentiated thyroid cancer is limited. We analyzed the clinical factors associated with detected distant metastasis or anaplastic transformation following reoperation for differentiated thyroid cancer.
Methods:
This retrospective review included 336 patients who underwent reoperation for differentiated thyroid cancer with detection of distant metastasis or anaplastic transformation following reoperation. The hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated.
Results:
Distant metastasis was detected in 45 patients (45/336, 13.4%) after reoperation. The risk of distant metastasis was higher for patients of male sex (adjusted HR: 2.373; 95% CI: 1.133-4.973), age ≥ 55 (adjusted HR: 4.991; 95% CI: 2.451-10.165), initial T3-4 stage (adjusted HR: 2.347; 95% CI: 1.035-5.321), in-field recurrence (adjusted HR: 3.267; 95% CI: 1.489-7.168), and those who had undergone ≥ 3 reoperations (adjusted HR: 3.378; 95% CI: 1.248-9.174). Anaplastic transformation was detected in 7 patients (7/336, 2.1%) after reoperation. The risk of anaplastic transformation was higher for patients with an age ≥ 55 (adjusted HR: 6.811; 95% CI: 1.300-35.676) and those who had undergone ≥ 3 reoperations (adjusted HR: 5.672; 95% CI: 1.139-28.236).
Conclusion:
In recurrent/persistent differentiated thyroid cancer, distant metastasis or anaplastic transformation following reoperation is not insignificant. There may be increased risk of distant metastasis or anaplastic transformation with multiple reoperations in patients who are men, aged ≥ 55, or at the initial T3-T4 stage.
Level Of Evidence:
4.
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