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Utility of microdissected cytology smears for molecular analysis of thyroid malignancy

BACKGROUND: Molecular testing of thyroid fine‐needle aspirates has demonstrated value in cases of indeterminate cytology (Bethesda categories III, IV, and V) enabling optimized individual patient management leading to better outcomes with health economic benefits. For most molecular testing modaliti...

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Autores principales: Kumar, Gyanendra, Timmaraju, Venkata Arun, Song‐Yang, Joanna Wanmin, Repko, Brittany, Narick, Christina, Mireskandari, Alidad, Finkelstein, Sydney
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587978/
https://www.ncbi.nlm.nih.gov/pubmed/30548138
http://dx.doi.org/10.1002/dc.24100
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author Kumar, Gyanendra
Timmaraju, Venkata Arun
Song‐Yang, Joanna Wanmin
Repko, Brittany
Narick, Christina
Mireskandari, Alidad
Finkelstein, Sydney
author_facet Kumar, Gyanendra
Timmaraju, Venkata Arun
Song‐Yang, Joanna Wanmin
Repko, Brittany
Narick, Christina
Mireskandari, Alidad
Finkelstein, Sydney
author_sort Kumar, Gyanendra
collection PubMed
description BACKGROUND: Molecular testing of thyroid fine‐needle aspirates has demonstrated value in cases of indeterminate cytology (Bethesda categories III, IV, and V) enabling optimized individual patient management leading to better outcomes with health economic benefits. For most molecular testing modalities, including mutational panels and classifier analyses, part or all of a dedicated needle aspiration pass is required to obtain an adequate sample for testing. Our analysis, which is based on a combination approach (mutation detection and microRNA classifier status), has documented clinical validity and utility when performed on thyroid fine‐needle aspirates placed directly into RNA preservative fluid. Here we show that the combination approach can be extended to microdissected stained cytology slides provides the physician greater opportunity to resolve cytological indeterminacy. METHODS: Extracted nucleic acid from needle aspirate and corresponding cytology preparations of 47 thyroid nodules were analyzed using identical methodology and results were compared. RESULTS: Of 94 molecular analyses (47 mutational analyses, 47 microRNA classifier assessments based on a validated 10 marker panel) only 5 samples showed discordant results. CONCLUSION: These findings, together with supplementary work using archival specimens shows that the combination approach can be effectively applied to both direct aspirated thyroid nodule aspirates or to nucleic acid extracted from macrodissected and microdissected cytology slide smears, with the expectation of equivalent results. The advantages of both specimen sources, direct aspirate, and cytology slide smears are discussed.
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spelling pubmed-65879782019-07-02 Utility of microdissected cytology smears for molecular analysis of thyroid malignancy Kumar, Gyanendra Timmaraju, Venkata Arun Song‐Yang, Joanna Wanmin Repko, Brittany Narick, Christina Mireskandari, Alidad Finkelstein, Sydney Diagn Cytopathol Original Articles BACKGROUND: Molecular testing of thyroid fine‐needle aspirates has demonstrated value in cases of indeterminate cytology (Bethesda categories III, IV, and V) enabling optimized individual patient management leading to better outcomes with health economic benefits. For most molecular testing modalities, including mutational panels and classifier analyses, part or all of a dedicated needle aspiration pass is required to obtain an adequate sample for testing. Our analysis, which is based on a combination approach (mutation detection and microRNA classifier status), has documented clinical validity and utility when performed on thyroid fine‐needle aspirates placed directly into RNA preservative fluid. Here we show that the combination approach can be extended to microdissected stained cytology slides provides the physician greater opportunity to resolve cytological indeterminacy. METHODS: Extracted nucleic acid from needle aspirate and corresponding cytology preparations of 47 thyroid nodules were analyzed using identical methodology and results were compared. RESULTS: Of 94 molecular analyses (47 mutational analyses, 47 microRNA classifier assessments based on a validated 10 marker panel) only 5 samples showed discordant results. CONCLUSION: These findings, together with supplementary work using archival specimens shows that the combination approach can be effectively applied to both direct aspirated thyroid nodule aspirates or to nucleic acid extracted from macrodissected and microdissected cytology slide smears, with the expectation of equivalent results. The advantages of both specimen sources, direct aspirate, and cytology slide smears are discussed. John Wiley & Sons, Inc. 2018-12-08 2019-04 /pmc/articles/PMC6587978/ /pubmed/30548138 http://dx.doi.org/10.1002/dc.24100 Text en © 2018 The Authors. Diagnostic Cytopathology published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://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
Kumar, Gyanendra
Timmaraju, Venkata Arun
Song‐Yang, Joanna Wanmin
Repko, Brittany
Narick, Christina
Mireskandari, Alidad
Finkelstein, Sydney
Utility of microdissected cytology smears for molecular analysis of thyroid malignancy
title Utility of microdissected cytology smears for molecular analysis of thyroid malignancy
title_full Utility of microdissected cytology smears for molecular analysis of thyroid malignancy
title_fullStr Utility of microdissected cytology smears for molecular analysis of thyroid malignancy
title_full_unstemmed Utility of microdissected cytology smears for molecular analysis of thyroid malignancy
title_short Utility of microdissected cytology smears for molecular analysis of thyroid malignancy
title_sort utility of microdissected cytology smears for molecular analysis of thyroid malignancy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587978/
https://www.ncbi.nlm.nih.gov/pubmed/30548138
http://dx.doi.org/10.1002/dc.24100
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