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BRAF Testing in Multifocal Papillary Thyroid Carcinoma

Background. BRAF V600E mutation is associated with poor prognosis in patients with papillary thyroid carcinoma (PTC). PTC is often multifocal, and there are no guidelines on how many tumors to test for BRAF mutation in multifocal PTC. Methods. Fifty-seven separate formalin-fixed and paraffin-embedde...

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Autores principales: Kimbrell, Hillary Z., Sholl, Andrew B., Ratnayaka, Swarnamala, Japa, Shanker, Lacey, Michelle, Carpio, Gandahari, Bhatia, Parisha, Kandil, Emad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4584030/
https://www.ncbi.nlm.nih.gov/pubmed/26448939
http://dx.doi.org/10.1155/2015/486391
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author Kimbrell, Hillary Z.
Sholl, Andrew B.
Ratnayaka, Swarnamala
Japa, Shanker
Lacey, Michelle
Carpio, Gandahari
Bhatia, Parisha
Kandil, Emad
author_facet Kimbrell, Hillary Z.
Sholl, Andrew B.
Ratnayaka, Swarnamala
Japa, Shanker
Lacey, Michelle
Carpio, Gandahari
Bhatia, Parisha
Kandil, Emad
author_sort Kimbrell, Hillary Z.
collection PubMed
description Background. BRAF V600E mutation is associated with poor prognosis in patients with papillary thyroid carcinoma (PTC). PTC is often multifocal, and there are no guidelines on how many tumors to test for BRAF mutation in multifocal PTC. Methods. Fifty-seven separate formalin-fixed and paraffin-embedded PTCs from twenty-seven patients were manually macrodissected and tested for BRAF mutation using a commercial allele-specific real-time polymerase chain reaction-based assay (Entrogen, Woodland Hills, CA). Data related to histologic characteristics, patient demographics, and clinical outcomes were collected. Results. All mutations detected were BRAF V600E. Seventeen patients (63%) had concordant mutation status in the largest and second-largest tumors (i.e., both were positive or both were negative). The remaining ten patients (37%) had discordant mutation status. Six of the patients with discordant tumors (22% overall) had a BRAF-negative largest tumor and a BRAF-positive second-largest tumor. No histologic feature was found to help predict which cases would be discordant. Conclusions. Patients with multifocal PTC whose largest tumor is BRAF-negative can have smaller tumors that are BRAF-positive. Therefore, molecular testing of more than just the dominant tumor should be considered. Future studies are warranted to establish whether finding a BRAF mutation in a smaller tumor has clinical significance.
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spelling pubmed-45840302015-10-07 BRAF Testing in Multifocal Papillary Thyroid Carcinoma Kimbrell, Hillary Z. Sholl, Andrew B. Ratnayaka, Swarnamala Japa, Shanker Lacey, Michelle Carpio, Gandahari Bhatia, Parisha Kandil, Emad Biomed Res Int Clinical Study Background. BRAF V600E mutation is associated with poor prognosis in patients with papillary thyroid carcinoma (PTC). PTC is often multifocal, and there are no guidelines on how many tumors to test for BRAF mutation in multifocal PTC. Methods. Fifty-seven separate formalin-fixed and paraffin-embedded PTCs from twenty-seven patients were manually macrodissected and tested for BRAF mutation using a commercial allele-specific real-time polymerase chain reaction-based assay (Entrogen, Woodland Hills, CA). Data related to histologic characteristics, patient demographics, and clinical outcomes were collected. Results. All mutations detected were BRAF V600E. Seventeen patients (63%) had concordant mutation status in the largest and second-largest tumors (i.e., both were positive or both were negative). The remaining ten patients (37%) had discordant mutation status. Six of the patients with discordant tumors (22% overall) had a BRAF-negative largest tumor and a BRAF-positive second-largest tumor. No histologic feature was found to help predict which cases would be discordant. Conclusions. Patients with multifocal PTC whose largest tumor is BRAF-negative can have smaller tumors that are BRAF-positive. Therefore, molecular testing of more than just the dominant tumor should be considered. Future studies are warranted to establish whether finding a BRAF mutation in a smaller tumor has clinical significance. Hindawi Publishing Corporation 2015 2015-09-13 /pmc/articles/PMC4584030/ /pubmed/26448939 http://dx.doi.org/10.1155/2015/486391 Text en Copyright © 2015 Hillary Z. Kimbrell et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Kimbrell, Hillary Z.
Sholl, Andrew B.
Ratnayaka, Swarnamala
Japa, Shanker
Lacey, Michelle
Carpio, Gandahari
Bhatia, Parisha
Kandil, Emad
BRAF Testing in Multifocal Papillary Thyroid Carcinoma
title BRAF Testing in Multifocal Papillary Thyroid Carcinoma
title_full BRAF Testing in Multifocal Papillary Thyroid Carcinoma
title_fullStr BRAF Testing in Multifocal Papillary Thyroid Carcinoma
title_full_unstemmed BRAF Testing in Multifocal Papillary Thyroid Carcinoma
title_short BRAF Testing in Multifocal Papillary Thyroid Carcinoma
title_sort braf testing in multifocal papillary thyroid carcinoma
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4584030/
https://www.ncbi.nlm.nih.gov/pubmed/26448939
http://dx.doi.org/10.1155/2015/486391
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