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Prospective Analysis of TERT Promoter Mutations in Papillary Thyroid Carcinoma at a Single Institution
Background: Papillary thyroid cancer (PTC) has the highest cancer incidence in Korea. It is known that some thyroid cancers have aggressive clinical behavior and a poor prognosis. Genomic studies have described some somatic mutations that are related to the aggressive features of thyroid cancer, suc...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8158380/ https://www.ncbi.nlm.nih.gov/pubmed/34070093 http://dx.doi.org/10.3390/jcm10102179 |
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author | Choi, Yun-Suk Choi, Seong-Woon Yi, Jin-Wook |
author_facet | Choi, Yun-Suk Choi, Seong-Woon Yi, Jin-Wook |
author_sort | Choi, Yun-Suk |
collection | PubMed |
description | Background: Papillary thyroid cancer (PTC) has the highest cancer incidence in Korea. It is known that some thyroid cancers have aggressive clinical behavior and a poor prognosis. Genomic studies have described some somatic mutations that are related to the aggressive features of thyroid cancer, such as the BRAF(V600E) mutation. Recently, TERT promoter mutations were identified and reported as poor prognostic factors in PTC. Our aim was to identify the frequency and clinical impact of TERT promoter mutation in PTC. Methods: Analysis of both BRAF(V600E) and TERT promoter mutations in thyroidectomy specimens began in February 2019. As of December 2020, 622 patients had been tested. Data were prospectively collected and retrospectively reviewed to ascertain clinical and pathologic variables. Results: TERT promoter mutations were identified in 13 patients (2.09%); 12 had the C228T mutation, and one had the C216T mutation. In total, ten patients had the BRAF(V600E) mutation. TERT promoter mutation was significantly associated with advanced age (46.795 ± 12.616 versus 65.692 ± 13.628 years, p < 0.001), large tumor size (1.006 ± 0.829 versus 2.285 ± 1.938 cm, p = 0.035), extrathyroidal extension, surgical margin involvement, angioinvasion, BRAF(V600E) mutation and advanced TNM stage, a higher MACIS score and a high proportion of radioactive iodine therapy application. Logistic regression showed that lymphatic and angioinvasion and BRAF(V600E) mutation were predictive of TERT promoter mutation. Conclusions: Our study is the first to report the prospective results of TERT promoter mutations at a single tertiary hospital in Incheon, Korea. PTC with TERT promoter mutation was associated with more aggressive behavior than PTC with wild-type TERT gene status. |
format | Online Article Text |
id | pubmed-8158380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81583802021-05-28 Prospective Analysis of TERT Promoter Mutations in Papillary Thyroid Carcinoma at a Single Institution Choi, Yun-Suk Choi, Seong-Woon Yi, Jin-Wook J Clin Med Article Background: Papillary thyroid cancer (PTC) has the highest cancer incidence in Korea. It is known that some thyroid cancers have aggressive clinical behavior and a poor prognosis. Genomic studies have described some somatic mutations that are related to the aggressive features of thyroid cancer, such as the BRAF(V600E) mutation. Recently, TERT promoter mutations were identified and reported as poor prognostic factors in PTC. Our aim was to identify the frequency and clinical impact of TERT promoter mutation in PTC. Methods: Analysis of both BRAF(V600E) and TERT promoter mutations in thyroidectomy specimens began in February 2019. As of December 2020, 622 patients had been tested. Data were prospectively collected and retrospectively reviewed to ascertain clinical and pathologic variables. Results: TERT promoter mutations were identified in 13 patients (2.09%); 12 had the C228T mutation, and one had the C216T mutation. In total, ten patients had the BRAF(V600E) mutation. TERT promoter mutation was significantly associated with advanced age (46.795 ± 12.616 versus 65.692 ± 13.628 years, p < 0.001), large tumor size (1.006 ± 0.829 versus 2.285 ± 1.938 cm, p = 0.035), extrathyroidal extension, surgical margin involvement, angioinvasion, BRAF(V600E) mutation and advanced TNM stage, a higher MACIS score and a high proportion of radioactive iodine therapy application. Logistic regression showed that lymphatic and angioinvasion and BRAF(V600E) mutation were predictive of TERT promoter mutation. Conclusions: Our study is the first to report the prospective results of TERT promoter mutations at a single tertiary hospital in Incheon, Korea. PTC with TERT promoter mutation was associated with more aggressive behavior than PTC with wild-type TERT gene status. MDPI 2021-05-18 /pmc/articles/PMC8158380/ /pubmed/34070093 http://dx.doi.org/10.3390/jcm10102179 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Choi, Yun-Suk Choi, Seong-Woon Yi, Jin-Wook Prospective Analysis of TERT Promoter Mutations in Papillary Thyroid Carcinoma at a Single Institution |
title | Prospective Analysis of TERT Promoter Mutations in Papillary Thyroid Carcinoma at a Single Institution |
title_full | Prospective Analysis of TERT Promoter Mutations in Papillary Thyroid Carcinoma at a Single Institution |
title_fullStr | Prospective Analysis of TERT Promoter Mutations in Papillary Thyroid Carcinoma at a Single Institution |
title_full_unstemmed | Prospective Analysis of TERT Promoter Mutations in Papillary Thyroid Carcinoma at a Single Institution |
title_short | Prospective Analysis of TERT Promoter Mutations in Papillary Thyroid Carcinoma at a Single Institution |
title_sort | prospective analysis of tert promoter mutations in papillary thyroid carcinoma at a single institution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8158380/ https://www.ncbi.nlm.nih.gov/pubmed/34070093 http://dx.doi.org/10.3390/jcm10102179 |
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