Detection of Circulating Tumor DNA in Patients with Thyroid Nodules

Objective. Detection of circulating tumor DNA (ctDNA) in cancer patients can potentially serve as a noninvasive, sensitive test of disease status. The purpose of this study was to determine the ability to detect BRAF (V600E) mutations in the plasma of patients with thyroid nodules, with the goal of...

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Main Authors: Krupal B. Patel, Nicholas Cormier, James Fowler, Allison Partridge, Julie Theurer, Morgan Black, Nicole Pinto, John Yoo, Kevin Fung, Danielle MacNeil, William Stecho, Christopher Howlett, Muriel Brackstone, John W. Barrett, Anthony Nichols
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:International Journal of Endocrinology
Online Access:http://dx.doi.org/10.1155/2021/8909224
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author Krupal B. Patel
Nicholas Cormier
James Fowler
Allison Partridge
Julie Theurer
Morgan Black
Nicole Pinto
John Yoo
Kevin Fung
Danielle MacNeil
William Stecho
Christopher Howlett
Muriel Brackstone
John W. Barrett
Anthony Nichols
author_facet Krupal B. Patel
Nicholas Cormier
James Fowler
Allison Partridge
Julie Theurer
Morgan Black
Nicole Pinto
John Yoo
Kevin Fung
Danielle MacNeil
William Stecho
Christopher Howlett
Muriel Brackstone
John W. Barrett
Anthony Nichols
author_sort Krupal B. Patel
collection DOAJ
description Objective. Detection of circulating tumor DNA (ctDNA) in cancer patients can potentially serve as a noninvasive, sensitive test of disease status. The purpose of this study was to determine the ability to detect BRAF (V600E) mutations in the plasma of patients with thyroid nodules, with the goal of distinguishing between benign and malignant nodules. Methods. Consecutive patients with thyroid nodules who consented for surgery were recruited. Plasma samples were obtained preoperatively and one month postoperatively. Quantitative PCR was used to determine the levels of the BRAF (V600E) mutation preoperatively and postoperatively. Results. A total of 109 patients were recruited. On final pathology, 38 (32.8%) patients had benign thyroid nodules, 45 (38.8%) had classical papillary thyroid cancer (PTC), 23 (19.8%) had nonclassical PTC, and 3 (2.6%) had follicular thyroid cancer. 15/109 patients had detectable BRAF (V600E) ctDNA in their preoperative samples—all of them having classical PTC. Higher T-stage and extrathyroidal extension in PTC were associated with positive BRAF (V600E) ctDNA (p<0.05). Eighty-eight pairs of preoperative and postoperative plasma samples were collected and analyzed. Of these eighty-eight paired samples, a total of 13/88 (14.8%) patients had detectable BRAF (V600E) ctDNA in their preoperative samples—all of them having classical PTC. 12 of these 13 patients had no detectable BRAF (V600E) postoperatively, while one remaining patient had a significant decline in his levels (p<0.05). Conclusion. BRAF (V600E) circulating thyroid tumor DNA can be detected in plasma and is correlated with a final diagnosis of the classical variant of PTC. Given that a postoperative drop in BRAF (V600E) ctDNA levels was observed in all cases suggests its utility as a tumor marker.
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spelling doaj-art-2567bb119caf44adb2a35dc6bbfd248a2025-02-03T01:25:16ZengWileyInternational Journal of Endocrinology1687-83371687-83452021-01-01202110.1155/2021/89092248909224Detection of Circulating Tumor DNA in Patients with Thyroid NodulesKrupal B. Patel0Nicholas Cormier1James Fowler2Allison Partridge3Julie Theurer4Morgan Black5Nicole Pinto6John Yoo7Kevin Fung8Danielle MacNeil9William Stecho10Christopher Howlett11Muriel Brackstone12John W. Barrett13Anthony Nichols14Department of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Pathology, Western University, London, Ontario, CanadaDepartment of Pathology, Western University, London, Ontario, CanadaDepartment of Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaDepartment of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, CanadaObjective. Detection of circulating tumor DNA (ctDNA) in cancer patients can potentially serve as a noninvasive, sensitive test of disease status. The purpose of this study was to determine the ability to detect BRAF (V600E) mutations in the plasma of patients with thyroid nodules, with the goal of distinguishing between benign and malignant nodules. Methods. Consecutive patients with thyroid nodules who consented for surgery were recruited. Plasma samples were obtained preoperatively and one month postoperatively. Quantitative PCR was used to determine the levels of the BRAF (V600E) mutation preoperatively and postoperatively. Results. A total of 109 patients were recruited. On final pathology, 38 (32.8%) patients had benign thyroid nodules, 45 (38.8%) had classical papillary thyroid cancer (PTC), 23 (19.8%) had nonclassical PTC, and 3 (2.6%) had follicular thyroid cancer. 15/109 patients had detectable BRAF (V600E) ctDNA in their preoperative samples—all of them having classical PTC. Higher T-stage and extrathyroidal extension in PTC were associated with positive BRAF (V600E) ctDNA (p<0.05). Eighty-eight pairs of preoperative and postoperative plasma samples were collected and analyzed. Of these eighty-eight paired samples, a total of 13/88 (14.8%) patients had detectable BRAF (V600E) ctDNA in their preoperative samples—all of them having classical PTC. 12 of these 13 patients had no detectable BRAF (V600E) postoperatively, while one remaining patient had a significant decline in his levels (p<0.05). Conclusion. BRAF (V600E) circulating thyroid tumor DNA can be detected in plasma and is correlated with a final diagnosis of the classical variant of PTC. Given that a postoperative drop in BRAF (V600E) ctDNA levels was observed in all cases suggests its utility as a tumor marker.http://dx.doi.org/10.1155/2021/8909224
spellingShingle Krupal B. Patel
Nicholas Cormier
James Fowler
Allison Partridge
Julie Theurer
Morgan Black
Nicole Pinto
John Yoo
Kevin Fung
Danielle MacNeil
William Stecho
Christopher Howlett
Muriel Brackstone
John W. Barrett
Anthony Nichols
Detection of Circulating Tumor DNA in Patients with Thyroid Nodules
International Journal of Endocrinology
title Detection of Circulating Tumor DNA in Patients with Thyroid Nodules
title_full Detection of Circulating Tumor DNA in Patients with Thyroid Nodules
title_fullStr Detection of Circulating Tumor DNA in Patients with Thyroid Nodules
title_full_unstemmed Detection of Circulating Tumor DNA in Patients with Thyroid Nodules
title_short Detection of Circulating Tumor DNA in Patients with Thyroid Nodules
title_sort detection of circulating tumor dna in patients with thyroid nodules
url http://dx.doi.org/10.1155/2021/8909224
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