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Preoperative BRAF(V600E) mutation detection in thyroid carcinoma by immunocytochemistry
The BRAF(V600E) (BRAF) mutation is present in 40–50% of papillary thyroid carcinomas (PTC) and has been associated with more aggressive clinicopathological characteristics of PTC. The aim of this study was to evaluate different methods for preoperative identification of the BRAF mutation in PTC usin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804421/ https://www.ncbi.nlm.nih.gov/pubmed/35951496 http://dx.doi.org/10.1111/apm.13267 |
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author | Swan, Kristine Zøylner Madsen, Stine Horskær Bonnema, Steen Joop Nielsen, Viveque Egsgaard Jespersen, Marie Louise |
author_facet | Swan, Kristine Zøylner Madsen, Stine Horskær Bonnema, Steen Joop Nielsen, Viveque Egsgaard Jespersen, Marie Louise |
author_sort | Swan, Kristine Zøylner |
collection | PubMed |
description | The BRAF(V600E) (BRAF) mutation is present in 40–50% of papillary thyroid carcinomas (PTC) and has been associated with more aggressive clinicopathological characteristics of PTC. The aim of this study was to evaluate different methods for preoperative identification of the BRAF mutation in PTC using cytological and histological specimens. Prospectively collected preoperative cytological clots from patients with suspected PTC were tested with BRAF immunocytochemistry (ICC) and the Cobas Test (PCR). In addition, histological specimens were tested with BRAF immunohistochemistry (IHC) and the Cobas Test. All nodules were histologically examined. Fifty‐three patients were included in the study. Complete mutation testing was available in 32 patients. The main reason for exclusion was insufficient cell content in the cytological specimen. Twenty‐seven nodules were histologically diagnosed as PTC, and 41% (n = 11) of PTCs were BRAF ICC positive. All non‐PTC nodules were negative by BRAF ICC. In 26 nodules, all four BRAF tests were concordant, while discordant test results were found in six nodules. ICC was in accordance with the consensus BRAF status in five of these nodules, while BRAF status was undetermined in one nodule. BRAF ICC showed high concordance with the Cobas Test and a low rate of false negative stain. These results indicate that BRAF ICC may be a feasible method for preoperative detection of the BRAF(V600E) mutation in patients with PTC. |
format | Online Article Text |
id | pubmed-9804421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98044212023-01-03 Preoperative BRAF(V600E) mutation detection in thyroid carcinoma by immunocytochemistry Swan, Kristine Zøylner Madsen, Stine Horskær Bonnema, Steen Joop Nielsen, Viveque Egsgaard Jespersen, Marie Louise APMIS Original Articles The BRAF(V600E) (BRAF) mutation is present in 40–50% of papillary thyroid carcinomas (PTC) and has been associated with more aggressive clinicopathological characteristics of PTC. The aim of this study was to evaluate different methods for preoperative identification of the BRAF mutation in PTC using cytological and histological specimens. Prospectively collected preoperative cytological clots from patients with suspected PTC were tested with BRAF immunocytochemistry (ICC) and the Cobas Test (PCR). In addition, histological specimens were tested with BRAF immunohistochemistry (IHC) and the Cobas Test. All nodules were histologically examined. Fifty‐three patients were included in the study. Complete mutation testing was available in 32 patients. The main reason for exclusion was insufficient cell content in the cytological specimen. Twenty‐seven nodules were histologically diagnosed as PTC, and 41% (n = 11) of PTCs were BRAF ICC positive. All non‐PTC nodules were negative by BRAF ICC. In 26 nodules, all four BRAF tests were concordant, while discordant test results were found in six nodules. ICC was in accordance with the consensus BRAF status in five of these nodules, while BRAF status was undetermined in one nodule. BRAF ICC showed high concordance with the Cobas Test and a low rate of false negative stain. These results indicate that BRAF ICC may be a feasible method for preoperative detection of the BRAF(V600E) mutation in patients with PTC. John Wiley and Sons Inc. 2022-08-26 2022-11 /pmc/articles/PMC9804421/ /pubmed/35951496 http://dx.doi.org/10.1111/apm.13267 Text en © 2022 The Authors. APMIS published by John Wiley & Sons Ltd on behalf of Scandinavian Societies for Pathology, Medical Microbiology and Immunology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Swan, Kristine Zøylner Madsen, Stine Horskær Bonnema, Steen Joop Nielsen, Viveque Egsgaard Jespersen, Marie Louise Preoperative BRAF(V600E) mutation detection in thyroid carcinoma by immunocytochemistry |
title | Preoperative BRAF(V600E)
mutation detection in thyroid carcinoma by immunocytochemistry |
title_full | Preoperative BRAF(V600E)
mutation detection in thyroid carcinoma by immunocytochemistry |
title_fullStr | Preoperative BRAF(V600E)
mutation detection in thyroid carcinoma by immunocytochemistry |
title_full_unstemmed | Preoperative BRAF(V600E)
mutation detection in thyroid carcinoma by immunocytochemistry |
title_short | Preoperative BRAF(V600E)
mutation detection in thyroid carcinoma by immunocytochemistry |
title_sort | preoperative braf(v600e)
mutation detection in thyroid carcinoma by immunocytochemistry |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804421/ https://www.ncbi.nlm.nih.gov/pubmed/35951496 http://dx.doi.org/10.1111/apm.13267 |
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