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Local molecular analysis of indeterminate thyroid nodules
BACKGROUND: Thyroid nodules are common but only a minority are malignant. Molecular testing can assist in helping determine whether indeterminate nodules are suspicious for malignancy or benign. The objective of the study was to determine if the analysis of mutations (BRAF, NRAS, KRAS and HRAS) usin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666165/ https://www.ncbi.nlm.nih.gov/pubmed/26621130 http://dx.doi.org/10.1186/s40463-015-0106-2 |
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author | Gill, Mandeep S. Nayan, Smriti Kocovski, Linda Cutz, Jean-Claude Archibald, Stuart D. Jackson, Bernard S. Young, James E. M. Gupta, Michael K. |
author_facet | Gill, Mandeep S. Nayan, Smriti Kocovski, Linda Cutz, Jean-Claude Archibald, Stuart D. Jackson, Bernard S. Young, James E. M. Gupta, Michael K. |
author_sort | Gill, Mandeep S. |
collection | PubMed |
description | BACKGROUND: Thyroid nodules are common but only a minority are malignant. Molecular testing can assist in helping determine whether indeterminate nodules are suspicious for malignancy or benign. The objective of the study was to determine if the analysis of mutations (BRAF, NRAS, KRAS and HRAS) using readily available molecular techniques can help better classify indeterminate thyroid nodules. METHODS: A retrospective cohort of consecutive patients undergoing diagnostic thyroid surgery were analyzed for the presence or absence of specific mutations known to be associated with thyroid malignancy in FNA samples. Markers chosen were BRAF, NRAS, KRAS and HRAS. All were locally available and currently in use at our centre for other clinical indications. Results from the molecular analysis were then compared to the histopathology from thyroidectomy specimens to determine the sensitivity and specificity of these molecular techniques to classify indeterminate thyroid nodules. RESULTS: Sixty consecutive patients with indeterminate FNAs were recruited. Twenty-three patients had malignant tumors while 37 specimens were benign. Multiple different mutations were identified in the FNA samples. Overall 18 cases had a positive mutation (10 malignant and 8 benign). The sensitivity of BRAF, HRAS, KRAS, and NRAS was 8.7, 8.7, 8.7, and 17.4 respectively while the specificity was100, 83.7, 100 and 94.6. CONCLUSION: While molecular analysis remains promising, it requires further refinement. Several markers showed promise as good "rule-in" tests. |
format | Online Article Text |
id | pubmed-4666165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46661652015-12-02 Local molecular analysis of indeterminate thyroid nodules Gill, Mandeep S. Nayan, Smriti Kocovski, Linda Cutz, Jean-Claude Archibald, Stuart D. Jackson, Bernard S. Young, James E. M. Gupta, Michael K. J Otolaryngol Head Neck Surg Original Research Article BACKGROUND: Thyroid nodules are common but only a minority are malignant. Molecular testing can assist in helping determine whether indeterminate nodules are suspicious for malignancy or benign. The objective of the study was to determine if the analysis of mutations (BRAF, NRAS, KRAS and HRAS) using readily available molecular techniques can help better classify indeterminate thyroid nodules. METHODS: A retrospective cohort of consecutive patients undergoing diagnostic thyroid surgery were analyzed for the presence or absence of specific mutations known to be associated with thyroid malignancy in FNA samples. Markers chosen were BRAF, NRAS, KRAS and HRAS. All were locally available and currently in use at our centre for other clinical indications. Results from the molecular analysis were then compared to the histopathology from thyroidectomy specimens to determine the sensitivity and specificity of these molecular techniques to classify indeterminate thyroid nodules. RESULTS: Sixty consecutive patients with indeterminate FNAs were recruited. Twenty-three patients had malignant tumors while 37 specimens were benign. Multiple different mutations were identified in the FNA samples. Overall 18 cases had a positive mutation (10 malignant and 8 benign). The sensitivity of BRAF, HRAS, KRAS, and NRAS was 8.7, 8.7, 8.7, and 17.4 respectively while the specificity was100, 83.7, 100 and 94.6. CONCLUSION: While molecular analysis remains promising, it requires further refinement. Several markers showed promise as good "rule-in" tests. BioMed Central 2015-12-01 /pmc/articles/PMC4666165/ /pubmed/26621130 http://dx.doi.org/10.1186/s40463-015-0106-2 Text en © Gill et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Original Research Article Gill, Mandeep S. Nayan, Smriti Kocovski, Linda Cutz, Jean-Claude Archibald, Stuart D. Jackson, Bernard S. Young, James E. M. Gupta, Michael K. Local molecular analysis of indeterminate thyroid nodules |
title | Local molecular analysis of indeterminate thyroid nodules |
title_full | Local molecular analysis of indeterminate thyroid nodules |
title_fullStr | Local molecular analysis of indeterminate thyroid nodules |
title_full_unstemmed | Local molecular analysis of indeterminate thyroid nodules |
title_short | Local molecular analysis of indeterminate thyroid nodules |
title_sort | local molecular analysis of indeterminate thyroid nodules |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666165/ https://www.ncbi.nlm.nih.gov/pubmed/26621130 http://dx.doi.org/10.1186/s40463-015-0106-2 |
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