Literature DB >> 19574281

BRAF V600E mutation analysis increases diagnostic accuracy for papillary thyroid carcinoma in fine-needle aspiration biopsies.

Maria Chiara Zatelli1, Giorgio Trasforini, Stefania Leoni, Gemma Frigato, Mattia Buratto, Federico Tagliati, Roberta Rossi, Luigi Cavazzini, Elio Roti, Ettore C degli Uberti.   

Abstract

OBJECTIVE: Papillary thyroid carcinoma (PTC) represents the majority of differentiated thyroid cancers, presenting the V600E activating BRAF mutation in 29-83% of cases. The aim of our study is to analyze the influence of BRAF mutation analysis on the diagnostic accuracy of fine-needle aspiration biopsy (FNAB) in patients with suspected PTC. DESIGN AND METHODS: Thyroid cytoaspirates from 469 nodules (size: 1.1+/-0.8 cm) with ultrasonographic features suspicious of malignant lesion, performed in 374 patients, were submitted to cytological evaluation and to biomolecular analysis, carried out after somatic DNA isolation, specific PCR amplification, and subsequent automated direct sequencing. All PCR fragments were also processed by specific enzyme restriction analysis.
RESULTS: BRAF V600E mutation was found in 48 samples, 41 of which were also cytologically diagnosed as PTC, with histologic confirmation after thyroidectomy. Total thyroidectomy was perfomed also in seven patients with negative cytology but positive BRAF mutation, with histological confirmation of PTC in all. Among the 429 BRAF-negative samples, 407 had negative cytology for PTC, while 22 were diagnosed as suspected PTC and underwent total thyroidectomy with histological diagnosis of PTC in 17 and benign lesion in five. The prevalence of BRAF V600E mutation among histologically diagnosed PTC patients was 64%. Biomolecular analysis significantly increased cytology sensitivity for PTC from 77.3 to 86.7% (P<0.01).
CONCLUSIONS: These data indicate that BRAF V600E mutation analysis can significantly improve FNAB diagnostic accuracy. However, biomolecular analysis is complementary to cytology, which should always be performed.

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Year:  2009        PMID: 19574281     DOI: 10.1530/EJE-09-0353

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  41 in total

1.  Early onset acromegaly associated with a novel deletion in CDKN1B 5'UTR region.

Authors:  Silvia Sambugaro; Mauro Di Ruvo; Maria Rosaria Ambrosio; Natalia S Pellegata; Mariaenrica Bellio; Alessandra Guerra; Mattia Buratto; Maria Pia Foschini; Federico Tagliati; Ettore degli Uberti; Maria Chiara Zatelli
Journal:  Endocrine       Date:  2015-02-04       Impact factor: 3.633

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
Journal:  Endocrine       Date:  2014-01-23       Impact factor: 3.633

3.  Current concepts and future directions in differentiated thyroid cancer.

Authors:  Donald S A McLeod
Journal:  Clin Biochem Rev       Date:  2010-02

4.  An inexpensive, specific and highly sensitive protocol to detect the BrafV600E mutation in melanoma tumor biopsies and blood.

Authors:  David J Panka; Ryan J Sullivan; James W Mier
Journal:  Melanoma Res       Date:  2010-10       Impact factor: 3.599

Review 5.  Diagnostic biomarkers of differentiated thyroid cancer.

Authors:  Tada Kunavisarut
Journal:  Endocrine       Date:  2013-05-04       Impact factor: 3.633

6.  BRAF mutation analysis in thyroid nodules with indeterminate cytology: our experience on surgical management of patients with thyroid nodules from an area of borderline iodine deficiency.

Authors:  P Agretti; F Niccolai; T Rago; G De Marco; A Molinaro; M Scutari; C Di Cosmo; G Di Coscio; M Vitale; M Maccheroni; P Vitti; M Tonacchera
Journal:  J Endocrinol Invest       Date:  2014-09-07       Impact factor: 4.256

7.  Clinical utility of a blood-based BRAF(V600E) mutation assay in melanoma.

Authors:  David J Panka; Elizabeth Buchbinder; Anita Giobbie-Hurder; Aislyn P Schalck; Laleh Montaser-Kouhsari; Alireza Sepehr; Donald P Lawrence; David F McDermott; Rachel Cohen; Alexander Carlson; Jennifer A Wargo; Ryan Merritt; Virginia J Seery; F Stephen Hodi; Anasuya Gunturi; Dennie Fredrick; Michael B Atkins; A John Iafrate; Keith T Flaherty; James W Mier; Ryan J Sullivan
Journal:  Mol Cancer Ther       Date:  2014-10-15       Impact factor: 6.261

Review 8.  Values of molecular markers in the differential diagnosis of thyroid abnormalities.

Authors:  T M P B Tennakoon; M Rushdhi; A D C U Ranasinghe; R S Dassanayake
Journal:  J Cancer Res Clin Oncol       Date:  2016-12-22       Impact factor: 4.553

9.  Deletion of exons 1-3 of the MEN1 gene in a large Italian family causes the loss of menin expression.

Authors:  Maria Chiara Zatelli; Federico Tagliati; Mauro Di Ruvo; Emilie Castermans; Luigi Cavazzini; Adrian F Daly; Maria Rosaria Ambrosio; Albert Beckers; Ettore degli Uberti
Journal:  Fam Cancer       Date:  2014-06       Impact factor: 2.375

10.  Proposal for a novel management of indeterminate thyroid nodules on the basis of cytopathological subclasses.

Authors:  Martina Rossi; Sabrina Lupo; Roberta Rossi; Paola Franceschetti; Giorgio Trasforini; Stefania Bruni; Federico Tagliati; Mattia Buratto; Giovanni Lanza; Luca Damiani; Ettore Degli Uberti; Maria Chiara Zatelli
Journal:  Endocrine       Date:  2016-09-13       Impact factor: 3.633

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