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Hashimoto's Thyroiditis: A Protective Factor against Recurrence in BRAF-Wild Type Differentiated Thyroid Carcinoma
Peter P Issa1,2, Mahmoud Omar1, Yusef Buti1
1Department of Surgery, School of Medicine, Tulane University, New Orleans, LA 70112, USA.
Cancers
|May 16, 2023
Summary
Hashimoto's thyroiditis (HT) is a protective factor against differentiated thyroid carcinoma (DTC) recurrence, reducing risk by 70%. However, HT's protective effect is lost in BRAF-mutated tumors, highlighting a key difference in recurrence factors.
Area of Science:
- Endocrinology
- Oncology
- Pathology
Background:
- Hashimoto's thyroiditis (HT) is a known protective factor against lymph node metastasis in BRAF-mutated papillary thyroid carcinoma.
- The influence of HT on differentiated thyroid carcinoma (DTC) recurrence, particularly in the context of BRAF mutations, remains unclear.
Purpose of the Study:
- To investigate the effect of underlying HT on DTC recurrence.
- To analyze the impact of HT on BRAF-mutated DTC recurrence.
Main Methods:
- Retrospective analysis of 469 DTC patients.
- Stratification based on BRAF mutation and HT status.
- Multivariate regression analysis to identify risk and protective factors for recurrence.
Main Results:
- HT was associated with less aggressive tumors, including more microcarcinomas, less lymph node involvement, and significantly lower recurrence rates (2.9% vs. 11.9%).
- BRAF mutation correlated with increased lymph node involvement and nearly doubled recurrence rates (14.9% vs. 6.5%).
- HT was an independent protective factor, reducing recurrence odds by 70% (HR: 0.30). This protective effect was significant in BRAF-wild type tumors but not in BRAF-mutant tumors.
Conclusions:
- Underlying HT is an independent protective factor against DTC recurrence, significantly reducing risk.
- The protective role of HT against recurrence is maintained in BRAF-wild type DTC but is absent in BRAF-mutant DTC.
- HT status may enhance current risk stratification models for DTC patients, particularly considering BRAF mutation status.
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