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10.1186_s40463-021-00500-6.pdf 841,53KB
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1000 Titel
  • Molecular testing for cytologically suspicious and malignant (Bethesda V and VI) thyroid nodules to optimize the extent of surgical intervention: A retrospective chart review
1000 Autor/in
  1. Hier, Jessica |
  2. Avior, Galit |
  3. Pusztaszeri, Marc |
  4. Krasner, Joshua R. |
  5. Alyouha, Noura |
  6. Forest, Veronique-Isabelle |
  7. Hier, Michael P. |
  8. Mlynarek, Alex |
  9. Richardson, Keith |
  10. Sadeghi, Nader |
  11. Tamilia, Michael |
  12. Payne, Richard J. |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-01-01
1000 Erschienen in
1000 Quellenangabe
  • 50(1):29
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s40463-021-00500-6 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082804/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>Molecular testing has been used for cytologically indeterminate thyroid nodules (Bethesda III and IV), where the risk of malignancy is 10–40%. However, to date, the role of molecular testing in cytologically suspicious or positive for malignancy (Bethesda V and VI) thyroid nodules has been controversial. The aim of this study was to determine whether patients who had molecular testing in Bethesda V and VI thyroid nodules had the optimal extent of surgery performed more often than patients who did not have molecular testing performed.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>A retrospective chart review of 122 cases was performed: 101 patients from the McGill University teaching hospitals and 21 patients from the Hillel Yaffe Medical center, Technion University. Patients included in the study were those with Bethesda V or VI thyroid nodules who underwent molecular testing (ThyGenext® or ThyroseqV3®) (McGill <jats:italic>n</jats:italic> = 72, Hillel Yaffe <jats:italic>n</jats:italic> = 14). Patients with Bethesda V or VI thyroid nodules who did not undergo molecular testing were used as controls (McGill <jats:italic>n</jats:italic> = 29, Hillel Yaffe <jats:italic>n</jats:italic> = 7). Each case was reviewed in order to determine whether the patient had optimal surgery. This was defined as total thyroidectomy in the presence of either a positive lymph node, extrathyroidal extension, or an aggressive pathological variant of papillary thyroid carcinoma (tall cell, hobnail, columnar cell, diffuse sclerosing, and solid/trabecular) documented on the final pathology report. In all other cases, a lobectomy/hemi/subtotal thyroidectomy was considered as optimal surgery. Chi-squared testing was performed to compare groups.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>When molecular testing was done, 91.86% (79/86) of surgeries in the molecular testing group were optimal, compared to 61.11% (22/36) in the control group. At McGill University teaching hospitals and at Hillel Yaffe, 91.67% (66/72) and 92.86% (13/14) of surgeries in the intervention group were considered as optimal, respectively. This compares to 58.62% (17/29) at McGill and 71.43% (5/7) at Hillel Yaffe when molecular testing was not performed (<jats:italic>p</jats:italic> = .001, <jats:italic>p</jats:italic> = .186).</jats:p> </jats:sec><jats:sec> <jats:title>Conclusions</jats:title> <jats:p>In this study, molecular testing in Bethesda V and VI thyroid tumors significantly improved the likelihood of optimal surgery. Therefore, molecular testing may have an important role in optimizing surgical procedures performed in the setting of Bethesda V and VI thyroid nodules. Prospective studies with larger sample sizes are required to further investigate this finding.</jats:p> </jats:sec><jats:sec> <jats:title>Graphical abstract</jats:title> </jats:sec>
1000 Sacherschließung
lokal Thyroid Nodule/surgery [MeSH]
lokal Thyroid Nodule/pathology [MeSH]
lokal Female [MeSH]
lokal Mutation [MeSH]
lokal Aged [MeSH]
lokal Proto-Oncogene Proteins B-raf/genetics [MeSH]
lokal Humans [MeSH]
lokal Molecular Diagnostic Techniques [MeSH]
lokal Thyroidectomy [MeSH]
lokal Retrospective Studies [MeSH]
lokal Middle Aged [MeSH]
lokal Thyroid Neoplasms/genetics [MeSH]
lokal Thyroid Nodule/genetics [MeSH]
lokal Thyroid Neoplasms/pathology [MeSH]
lokal Thyroid Cancer, Papillary/pathology [MeSH]
lokal Male [MeSH]
lokal Thyroid Neoplasms/surgery [MeSH]
lokal Original Research Article
lokal Thyroid Cancer, Papillary/genetics [MeSH]
lokal Thyroid Cancer, Papillary/surgery [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-8764-8867|https://frl.publisso.de/adhoc/uri/QXZpb3IsIEdhbGl0|https://frl.publisso.de/adhoc/uri/UHVzenRhc3plcmksIE1hcmM=|https://frl.publisso.de/adhoc/uri/S3Jhc25lciwgSm9zaHVhIFIu|https://frl.publisso.de/adhoc/uri/QWx5b3VoYSwgTm91cmE=|https://frl.publisso.de/adhoc/uri/Rm9yZXN0LCBWZXJvbmlxdWUtSXNhYmVsbGU=|https://frl.publisso.de/adhoc/uri/SGllciwgTWljaGFlbCBQLg==|https://frl.publisso.de/adhoc/uri/TWx5bmFyZWssIEFsZXg=|https://frl.publisso.de/adhoc/uri/UmljaGFyZHNvbiwgS2VpdGg=|https://frl.publisso.de/adhoc/uri/U2FkZWdoaSwgTmFkZXI=|https://frl.publisso.de/adhoc/uri/VGFtaWxpYSwgTWljaGFlbA==|https://frl.publisso.de/adhoc/uri/UGF5bmUsIFJpY2hhcmQgSi4=
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