Department of Surgery, New York Presbyterian Hospital-Weill Cornell Medical College, New York, New York, USA.
Cancer. 2013 Apr 15;119(8):1495-502. doi: 10.1002/cncr.27888. Epub 2012 Dec 21.
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.
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.
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.
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.
术前 B 型 Raf 激酶 Val600Glu 突变(或 BRAF(V600E))分析被提议作为指导不确定甲状腺结节初始手术的工具。本研究旨在确定恶性细胞学标志物是否与 BRAF(V600E)突变相关,以及术前 BRAF(V600E)检测是否会改变不确定结节患者的初始治疗。
在一家三级保健中心,前瞻性招募了 2003 年至 2012 年间因甲状腺结节而接受手术的患者。对储存的结节样本进行 BRAF(V600E)突变的回顾性基因分型。检查 BRAF(V600E)状态、人口统计学、细胞学和组织病理学发现以及初始手术选择。
共纳入 960 例患者,其中 310 例(32%)为不确定结节。13 例(4%)患者存在 BRAF(V600E)突变,其中 12 例存在细胞学不典型或贝塞斯达分类 V。与贝塞斯达分类 III 或 IV 结节中 3%的恶性肿瘤携带该突变相比,贝塞斯达分类 V 恶性肿瘤中 42%携带该突变。核沟(P =.030)、假包涵体(P <.001)和椭圆形核(P =.022)在 BRAF(V600E)突变体中更为常见。单独使用 BRAF 检测、细胞学不典型/贝塞斯达分类 V 分类或两者的灵敏度分别为 15%、73%和 76%。13 例 BRAF(V600E)突变体中有 12 例最初因令人担忧的细胞学特征而进行全甲状腺切除术,因此如果术前进行 BRAF(V600E)检测,仅有一位患者的初始治疗会发生改变。
术前 BRAF(V600E)突变筛查不能显著改善风险分层,不太可能改变不确定结节患者的初始治疗。