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10.1186_s40463-019-0372-5.pdf 4,37MB
WeightNameValue
1000 Titel
  • Molecular mutations as a possible factor for determining extent of thyroid surgery
1000 Autor/in
  1. Krasner, Joshua R. |
  2. Alyouha, Nourah |
  3. Pusztaszeri, Marc |
  4. Forest, Veronique-Isabelle |
  5. Hier, Michael P. |
  6. Avior, Galit |
  7. Payne, Richard |
1000 Verlag
  • SAGE Publications
1000 Erscheinungsjahr 2019
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2019-01-01
1000 Erschienen in
1000 Quellenangabe
  • 48(1):51
1000 Copyrightjahr
  • 2019
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s40463-019-0372-5 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796357/ |
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 of thyroid nodules is a diagnostic tool used to better understand the nature of thyroid nodules. The aim of this study is to better comprehend the relationship between specific mutations and aggressive behavior of the tumour as demonstrated on postoperative pathological analysis.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods</jats:title> <jats:p>A retrospective chart review of 103 cases was performed. Included were patients who had undergone molecular testing using a panel that tests for 9 mutations (ThyGenX®) and were found to have malignant tumours. The following gene alterations were found pre-operatively in the nodules: <jats:italic>BRAF V600E</jats:italic> (<jats:italic>n</jats:italic> = 32), <jats:italic>BRAF K601E</jats:italic> (<jats:italic>n</jats:italic> = 4), <jats:italic>NRAS</jats:italic> (<jats:italic>n</jats:italic> = 11), <jats:italic>HRAS</jats:italic> (<jats:italic>n</jats:italic> = 4), <jats:italic>KRAS</jats:italic> (<jats:italic>n</jats:italic> = 3), <jats:italic>RET/PTC1</jats:italic> rearrangement (<jats:italic>n</jats:italic> = 1), <jats:italic>TERT</jats:italic> promoter (<jats:italic>n</jats:italic> = 2), <jats:italic>PAX8-PPARγ</jats:italic> rearrangement (<jats:italic>n</jats:italic> = 1), and 45 cases where no mutation was detected. Aggressive behavior was defined by extra-thyroidal extension (ETE), lymph node metastasis (LN+), and the following variants of papillary thyroid carcinoma: tall cell, solid, diffuse sclerosing, columnar cell and hobnail. Chi-squared testing was performed to compare groups.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>The group with <jats:italic>BRAF V600E, RET/PTC1</jats:italic> rearrangement, and <jats:italic>TERT</jats:italic> promoter mutations was associated with ETE 37.1%, and LN+ 45.7% of the time compared to 4.3 and 13.0% in the group with other mutations, and 4.4 and 4.4% in the group with no mutations (<jats:italic>p</jats:italic>-value 0.02, <jats:italic>p</jats:italic>-value &lt; 0.001, p-value 0.006). In addition, the <jats:italic>BRAF V600E, RET/PTC1</jats:italic> rearrangement<jats:italic>,</jats:italic> and <jats:italic>TERT</jats:italic> mutations group demonstrated tall cell variants (17.1%), columnar cell variants (5.7%), and hobnail variants (3%). The other mutations group demonstrated columnar cell variants (4.3%), and the no mutations group demonstrated solid variants (2.2%).</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions</jats:title> <jats:p>In this study, <jats:italic>BRAF V600E, RET/PTC1</jats:italic> rearrangement<jats:italic>,</jats:italic> and <jats:italic>TERT</jats:italic> mutations were associated with aggressive behaving thyroid malignancies as defined above. Molecular testing may be a useful method to anticipate aggressive tumour types and therefore assist in planning the extent and timing of surgery.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Thyroid Nodule/surgery [MeSH]
lokal Thyroid Nodule/pathology [MeSH]
lokal Female [MeSH]
lokal Molecular testing
lokal Telomerase/genetics [MeSH]
lokal Mutation [MeSH]
lokal Extent of surgery
lokal Aged [MeSH]
lokal Proto-Oncogene Proteins B-raf/genetics [MeSH]
lokal Humans [MeSH]
lokal Thyroid Gland/pathology [MeSH]
lokal Retrospective Studies [MeSH]
lokal Thyroid cancer
lokal Middle Aged [MeSH]
lokal Thyroid Nodule/genetics [MeSH]
lokal Proto-Oncogene Proteins c-ret/genetics [MeSH]
lokal Thyroidectomy/methods [MeSH]
lokal Male [MeSH]
lokal Thyroid Gland/surgery [MeSH]
lokal Original Research Article
lokal Analysis of Variance [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/S3Jhc25lciwgSm9zaHVhIFIu|https://frl.publisso.de/adhoc/uri/QWx5b3VoYSwgTm91cmFo|https://frl.publisso.de/adhoc/uri/UHVzenRhc3plcmksIE1hcmM=|https://frl.publisso.de/adhoc/uri/Rm9yZXN0LCBWZXJvbmlxdWUtSXNhYmVsbGU=|https://frl.publisso.de/adhoc/uri/SGllciwgTWljaGFlbCBQLg==|https://frl.publisso.de/adhoc/uri/QXZpb3IsIEdhbGl0|https://orcid.org/0000-0003-3987-8243
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