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Prognostic analysis of persistent disease in medium-to high-risk children and adolescents with differentiated thyroid carcinoma

  • Huanxin Liang , Jinsi Chen , Zhixiao Wei and Junhong Li EMAIL logo
Published/Copyright: November 18, 2025

Abstract

Objectives

This multicentre retrospective study aimed to characterise progression-free survival (PFS) patterns and identify clinicopathological factors associated with disease progression in childhood and adolescent differentiated thyroid carcinoma (caDTC) patients with intermediate-to high-risk persistent disease.

Methods

All patients underwent initial treatment comprising total or near-total thyroidectomy, followed by radioiodine therapy and thyroid-stimulating hormone suppression. Univariate analysis using the log-rank test was performed to evaluate prognostic factors associated with PFS in caDTC patients. The median follow-up duration was 56.1 months (range: 15–112 months).

Results

The 1-, 3-, and 5-year PFS rates among intermediate- and high-risk caDTC patients with persistent disease were 82 , 55, and 32 %, respectively. The median PFS in the structural/functional persistent disease (S/FPD) group was significantly shorter than that in the biochemical persistent disease group (21.5 vs. 51.0 months, p<0.001). High-risk American Thyroid Association (ATA) recurrence risk stratification, stimulated thyroglobulin (sTg) levels ≥ 32.9 ng/mL, and S/FPD response to initial radioiodine therapy (RIT) were significantly associated with poor PFS. The optimal sTg cut-off value for predicting S/FPD status was 32.9 ng/mL, with an area under the receiver operating characteristic curve of 0.76. Sensitivity and specificity were 68 and 88 %, respectively.

Conclusions

Among caDTC patients with intermediate-to high-risk persistent disease, those with high-risk ATA recurrence stratification, sTg levels ≥ 32.9 ng/mL, and S/FPD response to initial RIT might require more aggressive treatment and closer clinical surveillance.


Corresponding author: Junhong Li, The First Affiliated Hospital of Guangxi Medical University, Nanning, China, E-mail:

  1. Research ethics: Date: 2025-1-16. ID:2025-E0042.

  2. Informed consent: Not applicable.

  3. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  4. Use of Large Language Models, AI and Machine Learning Tools: None declared.

  5. Conflict of interest: The authors state no conflict of interest.

  6. Research funding: Guangxi Medical and Health Appropriate Technology Development and Application Project (Project Contract number: s2018077).

  7. Data availability: Not applicable.

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Received: 2025-04-21
Accepted: 2025-10-14
Published Online: 2025-11-18
Published in Print: 2025-12-17

© 2025 Walter de Gruyter GmbH, Berlin/Boston

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