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Approach to risk stratification for papillary thyroid carcinoma based on molecular profiling: institutional analysis

BACKGROUND: Currently, treatment recommendations for papillary thyroid carcinoma are not based on the genetic background causing tumourigenesis. The aim of the present study was to correlate the mutational profile of papillary thyroid carcinoma with clinical parameters of tumour aggressiveness, to e...

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Autores principales: Staubitz, Julia I, Müller, Celine, Heymans, Antonia, Merten, Christina, Roos, Bianca, Poplawski, Alicia, Ludt, Annekathrin, Strobl, Stephanie, Springer, Erik, Schad, Arno, Roth, Wilfried, Musholt, Thomas J, Hartmann, Nils
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162683/
https://www.ncbi.nlm.nih.gov/pubmed/37146205
http://dx.doi.org/10.1093/bjsopen/zrad029
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author Staubitz, Julia I
Müller, Celine
Heymans, Antonia
Merten, Christina
Roos, Bianca
Poplawski, Alicia
Ludt, Annekathrin
Strobl, Stephanie
Springer, Erik
Schad, Arno
Roth, Wilfried
Musholt, Thomas J
Hartmann, Nils
author_facet Staubitz, Julia I
Müller, Celine
Heymans, Antonia
Merten, Christina
Roos, Bianca
Poplawski, Alicia
Ludt, Annekathrin
Strobl, Stephanie
Springer, Erik
Schad, Arno
Roth, Wilfried
Musholt, Thomas J
Hartmann, Nils
author_sort Staubitz, Julia I
collection PubMed
description BACKGROUND: Currently, treatment recommendations for papillary thyroid carcinoma are not based on the genetic background causing tumourigenesis. The aim of the present study was to correlate the mutational profile of papillary thyroid carcinoma with clinical parameters of tumour aggressiveness, to establish recommendations for risk-stratified surgical treatment. METHOD: Papillary thyroid carcinoma tumour tissue of patients undergoing thyroid surgery at the University Medical Centre Mainz underwent analysis of BRAF, TERT promoter and RAS mutational status as well as potential RET and NTRK rearrangements. Mutation status was correlated with clinical course of disease. RESULTS: One hundred and seventy-one patients operated for papillary thyroid carcinoma were included. The median age was 48 years (range 8–85) and 69 per cent (118/171) of patients were females. One hundred and nine papillary thyroid carcinomas were BRAF-V600E mutant, 16 TERT promotor mutant and 12 RAS mutant; 12 papillary thyroid carcinomas harboured RET rearrangements and two papillary thyroid carcinomas showed NTRK rearrangements. TERT promoter mutant papillary thyroid carcinomas had a higher risk of distant metastasis (OR 51.3, 7.0 to 1048.2, P < 0.001) and radioiodine-refractory disease (OR 37.8, 9.9 to 169.5, P < 0.001). Concomitant BRAF and TERT promoter mutations increased the risk of radioiodine-refractory disease in papillary thyroid carcinoma (OR 21.7, 5.6 to 88.9, P < 0.001). RET rearrangements were associated with a higher count of tumour-affected lymph nodes (OR 7950.9, 233.7 to 270495.7, P < 0.001) but did not influence distant metastasis or radioiodine-refractory disease. CONCLUSIONS: Papillary thyroid carcinoma with concomitant BRAF-V600E and TERT promoter mutations demonstrated an aggressive course of disease, suggesting the need for a more extensive surgical strategy. RET rearrangement-positive papillary thyroid carcinoma did not affect the clinical outcome, potentially obviating the need for prophylactic lymphadenectomy.
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spelling pubmed-101626832023-05-06 Approach to risk stratification for papillary thyroid carcinoma based on molecular profiling: institutional analysis Staubitz, Julia I Müller, Celine Heymans, Antonia Merten, Christina Roos, Bianca Poplawski, Alicia Ludt, Annekathrin Strobl, Stephanie Springer, Erik Schad, Arno Roth, Wilfried Musholt, Thomas J Hartmann, Nils BJS Open Original Article BACKGROUND: Currently, treatment recommendations for papillary thyroid carcinoma are not based on the genetic background causing tumourigenesis. The aim of the present study was to correlate the mutational profile of papillary thyroid carcinoma with clinical parameters of tumour aggressiveness, to establish recommendations for risk-stratified surgical treatment. METHOD: Papillary thyroid carcinoma tumour tissue of patients undergoing thyroid surgery at the University Medical Centre Mainz underwent analysis of BRAF, TERT promoter and RAS mutational status as well as potential RET and NTRK rearrangements. Mutation status was correlated with clinical course of disease. RESULTS: One hundred and seventy-one patients operated for papillary thyroid carcinoma were included. The median age was 48 years (range 8–85) and 69 per cent (118/171) of patients were females. One hundred and nine papillary thyroid carcinomas were BRAF-V600E mutant, 16 TERT promotor mutant and 12 RAS mutant; 12 papillary thyroid carcinomas harboured RET rearrangements and two papillary thyroid carcinomas showed NTRK rearrangements. TERT promoter mutant papillary thyroid carcinomas had a higher risk of distant metastasis (OR 51.3, 7.0 to 1048.2, P < 0.001) and radioiodine-refractory disease (OR 37.8, 9.9 to 169.5, P < 0.001). Concomitant BRAF and TERT promoter mutations increased the risk of radioiodine-refractory disease in papillary thyroid carcinoma (OR 21.7, 5.6 to 88.9, P < 0.001). RET rearrangements were associated with a higher count of tumour-affected lymph nodes (OR 7950.9, 233.7 to 270495.7, P < 0.001) but did not influence distant metastasis or radioiodine-refractory disease. CONCLUSIONS: Papillary thyroid carcinoma with concomitant BRAF-V600E and TERT promoter mutations demonstrated an aggressive course of disease, suggesting the need for a more extensive surgical strategy. RET rearrangement-positive papillary thyroid carcinoma did not affect the clinical outcome, potentially obviating the need for prophylactic lymphadenectomy. Oxford University Press 2023-05-05 /pmc/articles/PMC10162683/ /pubmed/37146205 http://dx.doi.org/10.1093/bjsopen/zrad029 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of BJS Society Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Staubitz, Julia I
Müller, Celine
Heymans, Antonia
Merten, Christina
Roos, Bianca
Poplawski, Alicia
Ludt, Annekathrin
Strobl, Stephanie
Springer, Erik
Schad, Arno
Roth, Wilfried
Musholt, Thomas J
Hartmann, Nils
Approach to risk stratification for papillary thyroid carcinoma based on molecular profiling: institutional analysis
title Approach to risk stratification for papillary thyroid carcinoma based on molecular profiling: institutional analysis
title_full Approach to risk stratification for papillary thyroid carcinoma based on molecular profiling: institutional analysis
title_fullStr Approach to risk stratification for papillary thyroid carcinoma based on molecular profiling: institutional analysis
title_full_unstemmed Approach to risk stratification for papillary thyroid carcinoma based on molecular profiling: institutional analysis
title_short Approach to risk stratification for papillary thyroid carcinoma based on molecular profiling: institutional analysis
title_sort approach to risk stratification for papillary thyroid carcinoma based on molecular profiling: institutional analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162683/
https://www.ncbi.nlm.nih.gov/pubmed/37146205
http://dx.doi.org/10.1093/bjsopen/zrad029
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