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甲状腺结节细针穿刺样本中Real-Q BRAF V600E检测分析方法的评估

Evaluation of the Real-Q BRAF V600E Detection Assay in Fine-Needle Aspiration Samples of Thyroid Nodules.

作者信息

Park Kyung Sun, Oh Young L, Ki Chang-Seok, Kim Jong-Won

机构信息

Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

Department of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

出版信息

J Mol Diagn. 2015 Jul;17(4):431-7. doi: 10.1016/j.jmoldx.2015.03.006. Epub 2015 Apr 30.

Abstract

Recently, several molecular assays for detecting the BRAF V600E mutation in fine-needle aspiration (FNA) specimens have been developed. Herein, we tested 294 consecutive FNA samples from patients with thyroid nodules with the Real-Q BRAF V600E detection assay (Real-Q). These results were compared with an allele-specific PCR-based kit using dual-priming oligonucleotides (AS-PCR). Any discordant results between the two tests were also analyzed by mutant enrichment with 3'-modified oligonucleotide sequencing. A total of 128 cases were confirmed histologically; of these, 121 were diagnosed as papillary thyroid carcinoma (PTC). The BRAF mutation was detected by Real-Q and AS-PCR testing in 80.2% (95% CI, 71.9%-86.9%) and 76.9% (95% CI, 68.3%-84.0%), respectively, of FNA specimens with PTC. Combining the BRAF V600E molecular assays (Real-Q and AS-PCR) with cytological diagnoses of malignant and suspicious for malignant cells, the detection rates (sensitivity) of Real-Q and AS-PCR for diagnosis of PTC increased to 94.2% (95% CI, 88.4%-97.6%) and 92.6% (95% CI, 86.4%-96.5%), respectively. In conclusion, the detection of BRAF V600E mutations in PTC by Real-Q is compatible to that of AS-PCR.

摘要

最近,已经开发出几种用于检测细针穿刺(FNA)标本中BRAF V600E突变的分子检测方法。在此,我们使用Real-Q BRAF V600E检测方法(Real-Q)对294例连续的甲状腺结节患者的FNA样本进行了检测。将这些结果与使用双引物寡核苷酸的基于等位基因特异性PCR的试剂盒(AS-PCR)进行比较。还通过3'修饰寡核苷酸测序的突变富集分析了两种检测之间的任何不一致结果。共有128例经组织学确诊;其中,121例被诊断为甲状腺乳头状癌(PTC)。在PTC的FNA标本中,通过Real-Q和AS-PCR检测分别检测到BRAF突变的比例为80.2%(95%CI,71.9%-86.9%)和76.9%(95%CI,68.3%-84.0%)。将BRAF V600E分子检测方法(Real-Q和AS-PCR)与恶性和可疑恶性细胞的细胞学诊断相结合,Real-Q和AS-PCR对PTC诊断的检测率(敏感性)分别提高到94.2%(95%CI,88.4%-97.6%)和92.6%(95%CI,86.4%-96.5%)。总之,Real-Q检测PTC中BRAF V600E突变的结果与AS-PCR的结果相当。

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