Literature DB >> 23280049

Preoperative BRAF(V600E) mutation screening is unlikely to alter initial surgical treatment of patients with indeterminate thyroid nodules: a prospective case series of 960 patients.

David A Kleiman1, Matthew J Sporn, Toni Beninato, Michael J Crowley, Anvy Nguyen, Alessia Uccelli, Theresa Scognamiglio, Rasa Zarnegar, Thomas J Fahey.   

Abstract

BACKGROUND: Preoperative B-type Raf kinase Val600Glu mutation, or BRAF(V600E), analysis has been proposed as a tool to guide initial surgery for indeterminate thyroid nodules. This study sought to determine if cytologic markers of malignancy are associated with the BRAF(V600E) mutation and if preoperative BRAF(V600E) testing would alter the initial management of patients with indeterminate nodules.
METHODS: Patients who underwent surgery for a thyroid nodule between 2003 and 2012 at a tertiary care center were prospectively enrolled. Stored nodule samples were retrospectively genotyped for the BRAF(V600E) mutation. BRAF(V600E) status, demographics, cytologic and histopathologic findings, and choice of initial surgery were examined.
RESULTS: A total of 960 patients were enrolled, of which 310 (32%) had an indeterminate nodule. The BRAF(V600E) mutation was identified in 13 patients (4%), 12 of whom had either cytologic atypia or were Bethesda category V. Three percent of Bethesda category III or IV nodules that were malignant harbored the mutation compared with 42% of Bethesda category V malignancies. Nuclear grooves (P = .030), pseudoinclusions (P < .001), and oval nuclei (P = .022) were all more common among BRAF(V600E) mutants. The sensitivities of using BRAF testing alone, cytologic atypia/Bethesda category V classification, or both, were 15%, 73%, and 76%, respectively. Twelve of the 13 BRAF(V600E) mutants had total thyroidectomies initially due to worrisome cytologic features, and therefore the initial management of only one patient would have been altered if BRAF(V600E) testing had been performed preoperatively.
CONCLUSIONS: Preoperative mutation screening for BRAF(V600E) does not meaningfully improve risk stratification and is unlikely to alter the initial management of patients with indeterminate nodules.
Copyright © 2012 American Cancer Society.

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Year:  2012        PMID: 23280049     DOI: 10.1002/cncr.27888

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  14 in total

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2.  Additional BRAF mutation analysis may have additional diagnostic value in thyroid nodules with "suspicious for malignant" cytology alone even when the nodules do not show suspicious US features.

Authors:  Jae Young Seo; Eun-Kyung Kim; Jin Young Kwak
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3.  Association of Tumor Size With Histologic and Clinical Outcomes Among Patients With Cytologically Indeterminate Thyroid Nodules.

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Journal:  Gland Surg       Date:  2020-01

5.  An affordable immunohistochemical approach to estimate the prevalence of BRAFV600E in large cohort studies-establishing the baseline rate of BRAF mutation in an institutional series of papillary thyroid carcinoma from Thailand.

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6.  Tumor genotype determines phenotype and disease-related outcomes in thyroid cancer: a study of 1510 patients.

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7.  Cancer Risk Associated with Nuclear Atypia in Cytologically Indeterminate Thyroid Nodules: A Systematic Review and Meta-Analysis.

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Journal:  Thyroid       Date:  2017-12-21       Impact factor: 6.568

8.  Outcome of Subclassification of Indeterminate (Thy-3) Thyroid Cytology into Thy-3a and Thy-3f.

Authors:  Catherine Brophy; Rania Mehanna; Julie McCarthy; Antoinette Tuthill; Matthew S Murphy; Patrick Sheahan
Journal:  Eur Thyroid J       Date:  2015-10-27

9.  RAS Mutations in AUS/FLUS Cytology: Does it Have an Additional Role in BRAFV600E Mutation-Negative Nodules?

Authors:  Jung Hyun Yoon; Hyeong Ju Kwon; Hye Sun Lee; Eun-Kyung Kim; Hee Jung Moon; Jin Young Kwak
Journal:  Medicine (Baltimore)       Date:  2015-07       Impact factor: 1.889

10.  BRAF 1799T>A Mutation Frequency in Mexican Mestizo Patients with Papillary Thyroid Cancer.

Authors:  Fernando Fernández-Ramírez; Luis M Hurtado-López; Mario A López; Eva Martínez-Peñafiel; Norma E Herrera-González; Luis Kameyama; Omar Sepúlveda-Robles
Journal:  Biomed Res Int       Date:  2018-04-02       Impact factor: 3.411

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