The Combined Use of Fine-Needle Aspiration (FNA) and BRAF V600E Gene Testing: Can it Increase the Definitive Diagnosis Rate of Nodules Categorized as Bethesda III for Papillary Thyroid Carcinoma?

IF 1 4区 医学 Q3 SURGERY
American Surgeon Pub Date : 2024-12-01 Epub Date: 2024-07-24 DOI:10.1177/00031348241265143
Lu Lei, Shang Hong Qing, Li Wei, Fu Ma Mo Yang, Yao Xiao Xiang
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引用次数: 0

Abstract

Objective: This study aimed to analyze the malignant probability of thyroid nodules diagnosed as indeterminate cytology, including atypia of undetermined significance or follicular lesion of undetermined significance (AUS/FLUS), and investigate the diagnostic value of combining BRAF V600E gene testing within this classification.

Methods: We conducted a retrospective analysis of 126 patients who underwent fine-needle aspiration (FNA) examination of thyroid nodules and subsequent surgical treatment at Beijing Haidian Hospital between October 2021 and November 2022. Among them, there were 22 male and 104 female patients, aged between 18 and 75 years old. Surgical pathology results were considered the gold standard for diagnosing the nature of thyroid nodules, evaluating the malignant incidence of cytological results categorized as AUS/FLUS. Fisher's exact test and diagnostic test evaluation methods were used to analyze the discriminatory diagnostic efficacy of preoperative FNA combined with BRAF V600E gene testing for papillary thyroid carcinoma (PTC). Statistical analysis was performed using SPSS 22.0 software.

Results: In PTC patients, the BRAF V600E gene mutation rate was 87.93% (102/116). Within the category of FNA results as AUS/FLUS, the proportion of PTC was 60.00% (15/25). The specificity, sensitivity, positive predictive value, and negative predictive value of the BRAF V600E gene mutation in diagnosing PTC within the AUS/FLUS category were 10/10, 6/15, 6/6, and 10/19, respectively. The BRAF V600E gene mutation significantly increased the detection rate of PTC in patients classified under this cytology (P = 0.028, <0.05).

Conclusion: Preoperative FNA combined with BRAF V600E gene mutation testing significantly enhances the malignant detection rate of thyroid nodules diagnosed cytologically as AUS/FLUS. This combined approach provides a potent tool to improve diagnostic accuracy in this indeterminate classification.

联合使用细针抽吸术 (FNA) 和 BRAF V600E 基因检测:能否提高甲状腺乳头状癌 Bethesda III 结节的确诊率?
研究目的本研究旨在分析甲状腺结节细胞学诊断为不确定(包括意义未定的不典型性或意义未定的滤泡性病变(AUS/FLUS))的恶性概率,并探讨在该分类中结合BRAF V600E基因检测的诊断价值:我们对2021年10月至2022年11月期间在北京海淀医院接受甲状腺结节细针穿刺(FNA)检查和后续手术治疗的126例患者进行了回顾性分析。其中男性 22 人,女性 104 人,年龄在 18 岁至 75 岁之间。手术病理结果被认为是诊断甲状腺结节性质的金标准,评估细胞学结果归类为AUS/FLUS的恶性发生率。费雪精确检验和诊断检测评估方法用于分析术前 FNA 结合 BRAF V600E 基因检测对甲状腺乳头状癌(PTC)的鉴别诊断效果。统计分析使用 SPSS 22.0 软件进行:在PTC患者中,BRAF V600E基因突变率为87.93%(102/116)。在 FNA 结果为 AUS/FLUS 的类别中,PTC 的比例为 60.00%(15/25)。在 AUS/FLUS 类别中,BRAF V600E 基因突变诊断 PTC 的特异性、敏感性、阳性预测值和阴性预测值分别为 10/10、6/15、6/6 和 10/19。BRAF V600E 基因突变可显著提高该细胞学分类患者的 PTC 检出率(P = 0.028,结论:术前 FNA 联合 BRAF V600E 基因突变检测可显著提高细胞学诊断为 AUS/FLUS 的甲状腺结节的恶性检出率。这种联合方法为提高这种不确定分类的诊断准确性提供了有效工具。
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来源期刊
American Surgeon
American Surgeon 医学-外科
CiteScore
1.40
自引率
0.00%
发文量
623
期刊介绍: The American Surgeon is a monthly peer-reviewed publication published by the Southeastern Surgical Congress. Its area of concentration is clinical general surgery, as defined by the content areas of the American Board of Surgery: alimentary tract (including bariatric surgery), abdomen and its contents, breast, skin and soft tissue, endocrine system, solid organ transplantation, pediatric surgery, surgical critical care, surgical oncology (including head and neck surgery), trauma and emergency surgery, and vascular surgery.
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