Straccia Patrizia, Brunelli Chiara, Rossi Esther D, Lanza Paola, Martini Maurizio, Musarra Teresa, Lombardi Celestino Pio, Pontecorvi Alfredo, Fadda Guido
Division of Anatomic Pathology and Histology, Catholic University of Sacred Heart, Foundation "Agostino Gemelli" University Hospital, Rome, Italy.
Division of Endocrine Surgery, Catholic University of Sacred Heart, Foundation "Agostino Gemelli" University Hospital, Rome, Italy.
Cytopathology. 2019 Sep;30(5):460-467. doi: 10.1111/cyt.12690. Epub 2019 Apr 23.
The recently introduced monoclonal V600E antibody (clone VE1) is likely to be an alternative strategy for detecting this mutation in thyroid lesions. Although VE1 immunostaining and molecular methods used to assess papillary thyroid carcinoma in surgical specimens are in good agreement, evaluation of VE1 in cytology and cell block samples is rarely performed, and its diagnostic value in cytology has not been well established. In this study, we sought to determine if VE1 is suitable for fine needle aspiration (FNA) and cell block methods.
A total of 86 patients who had BRAF V600E mutations were investigated with molecular and immunocytochemical (ICC) analysis in 45 FNA and 41 cell blocks. In total, 83 (96.5%) patients underwent surgical treatment. Assessment of BRAF V600E mutation status was performed in 72 (83.7%) cases.
Among the 72 cases analysed, 54 cases agreed (ICC+/BRAF+ or ICC-/BRAF-), seven cases were false positive (ICC+/BRAF-) and 11 cases were false negative (ICC-/BRAF+). False negative cases were not detected in the cell block method. The statistical analysis showed that sensitivity and specificity of ICC for detecting the BRAF V600E mutation were 61% and 77% in FNA samples and 100% and 73% in cell block.
The use of antibody VE-1 is a reliable method and a negative result of VE1 immunostaining might help to save time and money, restricting the molecular test to antibody-positive cases only. The identification of the aggressive variants of papillary carcinoma might be enabled by the expression of the antibody in neoplastic cells with tall cell features.
最近引入的单克隆V600E抗体(克隆VE1)可能是检测甲状腺病变中这种突变的另一种策略。虽然用于评估手术标本中甲状腺乳头状癌的VE1免疫染色和分子方法一致性良好,但很少对细胞学和细胞块样本进行VE1评估,其在细胞学中的诊断价值尚未得到充分确立。在本研究中,我们试图确定VE1是否适用于细针穿刺(FNA)和细胞块方法。
对86例具有BRAF V600E突变的患者进行了分子和免疫细胞化学(ICC)分析,其中45例为FNA样本,41例为细胞块样本。共有83例(96.5%)患者接受了手术治疗。对72例(83.7%)病例进行了BRAF V600E突变状态评估。
在分析的72例病例中,54例结果一致(ICC+/BRAF+或ICC-/BRAF-),7例为假阳性(ICC+/BRAF-),11例为假阴性(ICC-/BRAF+)。细胞块方法未检测到假阴性病例。统计分析表明,ICC检测BRAF V600E突变的敏感性和特异性在FNA样本中分别为61%和77%,在细胞块样本中分别为100%和73%。
使用抗体VE-1是一种可靠的方法,VE1免疫染色阴性结果可能有助于节省时间和金钱,仅将分子检测限于抗体阳性病例。肿瘤细胞中该抗体的表达可能有助于识别具有高细胞特征的乳头状癌侵袭性变体。