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Prognostic Implications of Maintaining the Target Thyroid-Stimulating Hormone Status Based on the 2015 American Thyroid Association Guidelines in Patients with Low-Risk Papillary Thyroid Carcinoma After Lobectomy: A 5-Year Landmark Analysis

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2024 Oct 16
PMID 39409875
Authors
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Abstract

: The 2015 American Thyroid Association guidelines recommend the maintenance of serum thyroid stimulating hormone (TSH) levels ≤2 mIU/L in patients with low-risk papillary thyroid carcinoma (PTC) who underwent lobectomy; however, the evidence is insufficient. We investigated the association between maintaining the TSH status at ≤2 mIU/L and tumor recurrence in patients with low-risk PTC who underwent lobectomy through a 5-year landmark analysis. : Between 2010 and 2016, 662 patients with low-risk PTC were included. The postoperative TSH status was determined using the 'TSH > 2 ratio', which was calculated using the TSH test results during the 5-year follow-up. The optimal cutoff value of 'TSH > 2 ratio' for tumor recurrence was determined using a receiver operating characteristic curve analysis. Recurrence-free survival (RFS) was compared between the groups using Kaplan-Meier and Cox proportional hazard regression analyses. : Patients with 'TSH > 2 ratio' > 0.1833 ( = 498) had a worse RFS outcome compared to patients with 'TSH > 2 ratio' ≤ 0.1833 ( = 164; < 0.001). 'TSH > 2 ratio' > 0.1833 was a significant risk factor for tumor recurrence after the 5-year landmark (hazard ratio: 4.795, 95% confidence interval: 2.102-10.937, < 0.001). : Maintaining TSH levels ≤ 2 mIU/L below a certain percentage among the total TSH tests during the 5-year follow-up period has a negative impact on tumor recurrence.

References
1.
Pelizzo M, Dobrinja C, Casal Ide E, Zane M, Lora O, Toniato A . The role of BRAF(V600E) mutation as poor prognostic factor for the outcome of patients with intrathyroid papillary thyroid carcinoma. Biomed Pharmacother. 2014; 68(4):413-7. DOI: 10.1016/j.biopha.2014.03.008. View

2.
Brabant G . Thyrotropin suppressive therapy in thyroid carcinoma: what are the targets?. J Clin Endocrinol Metab. 2008; 93(4):1167-9. DOI: 10.1210/jc.2007-2228. View

3.
Davies L, Welch H . Increasing incidence of thyroid cancer in the United States, 1973-2002. JAMA. 2006; 295(18):2164-7. DOI: 10.1001/jama.295.18.2164. View

4.
Lee E, Kang Y, Park Y, Koo B, Chung K, Ku E . A Multicenter, Randomized, Controlled Trial for Assessing the Usefulness of Suppressing Thyroid Stimulating Hormone Target Levels after Thyroid Lobectomy in Low to Intermediate Risk Thyroid Cancer Patients (MASTER): A Study Protocol. Endocrinol Metab (Seoul). 2021; 36(3):574-581. PMC: 8258337. DOI: 10.3803/EnM.2020.943. View

5.
Potter E, Horn R, Scheumann G, Dralle H, Costagliola S, Ludgate M . Western blot analysis of thyrotropin receptor expression in human thyroid tumours and correlation with TSH-binding. Biochem Biophys Res Commun. 1994; 205(1):361-7. DOI: 10.1006/bbrc.1994.2673. View