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갑상선 유두암의 예후 예측 인자로서 BRAF<sup>V600E</sup> 돌연변이의 역할

Role of BRAF<sup>V600E</sup> Mutation as a Marker for Prognostic Stratification of Papillary Thyroid Carcinoma

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Purpose: Papillary thyroid carcinoma (PTC) is the most common malignant tumor of the thyroid and BRAF<sup>V600E</sup> mutation is the most frequent genetic alteration in PTC. BRAF<sup>V600E</sup>mutation has been demonstrated as a prognostic biomarker for prediction of poor clinicopathological outcomes, such as increased incidence of extrathyroidal extension, lymph node metastasis, and advanced stage. However, there is conflicting literature regarding the association of BRAF<sup>V600E</sup> mutation and aggressive clinicopathological features. In this study, we investigated the prevalence of BRAF<sup>V600E</sup> mutation in PTC and determined the association of BRAF mutation with indicators of poor prognosis for PTC.Methods: We reviewed 1009 patients with PTC, who underwent thyroid surgery at Kyungpook National University Hospital between January 2013 and March 2014. BRAF<sup>V600E</sup> mutation analysis was performed using real-time polymerase chain reaction based amplification of DNA extracted from paraffin-embedded tumor specimens. Results: BRAF<sup>V600E</sup> mutation was detected in 863 (85.5%) patients. In univariate analysis, histologic subtype, extrathyroidal extension, and advanced stage showed significant association with BRAF<sup>V600E</sup> mutation. In addition, concurrent Hashimoto’s thyroiditis showed an association with low prevalence of BRAF<sup>V600E</sup> mutation. However, no stati-stically significant association was observed for age, gender, multifocal or bilateral tumor, and lymph node metastasis. Multivariate analysis showed an independent association of extrathyroidal extension with BRAF<sup>V600E</sup> mutation.Conclusion: In this study, extrathyroidal extension of PTC is an independent prognostic factor associated with BRAF<sup>V600E</sup> mutation status. However, conduct of further large scale studies with long term follow up is required before the BRAF mutation can be conclusively recommended as a prognostic biomarker.

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