Immunohistochemistry is highly sensitive and specific for the detection of V600E BRAF mutation in melanoma.
免疫组织化学检测黑色素瘤中V600E BRAF基因突变状况具有高度敏感性和特异性
Long GV,Wilmott JS,Capper D,Preusser M,Zhang YE,Thompson JF,Kefford RF,von Deimling A,Scolyer RA
Abstract
This study investigated the sensitivity and specificity of immunohistochemical (IHC) analysis using an anti-BRAF antibody to detect the presence of the BRAF V600E mutation in patients with metastatic melanoma. A total of 100 patients with American Joint Committee on Cancer stage IIIC unresectable or stage IV melanoma and who underwent tumor DNA BRAF mutation testing were selected. Paraffin-embedded, formalin-fixed melanoma biopsies were analyzed for the BRAF mutation status by independent, blinded observers using both conventional DNA molecular techniques and IHC with the novel BRAF V600E mutant-specific antibody, VE1. The antibody had a sensitivity of 97% (37/38) and a specificity of 98% (58/59) for detecting the presence of a BRAF V600E mutation. Of the BRAF-mutated cases, none of the non-V600E cases (including V600K) stained positive with the antibody (0/11). There were 5 cases with discordant BRAF mutation results. Additional molecular analysis confirmed the immunohistochemically obtained BRAF result in 3 cases, suggesting that the initial molecular testing results were incorrect. Two of these patients would not have received a BRAF inhibitor on the basis of the initial false-negative mutation testing result. Two cases remained discordant. The reported IHC method is an accurate, rapid, and cost-effective method for detecting V600E BRAF mutations in melanoma patients. Clinical use of the V600E BRAF antibody should be a valuable supplement to conventional mutation testing and allow V600E mutant metastatic melanoma patients to be triaged rapidly into appropriate treatment pathways.
摘要
这项研究针对存在BRAF V600E基因突变的转移性黑色素瘤患者进行了抗-BRAF抗体的免疫组织化学检测,进而分析其敏感性及特异性。总共纳入了100例美国癌症联合委员会IIIC期不可切除或IV期黑色素瘤并且进行了肿瘤DNA BRAF基因突变检测的患者。独立分析石蜡包埋、福尔马林固定黑色素瘤活检组织中BRAF基因的突变状态,应用常规的DNA分子技术及IHC技术(新的BRAF V600E突变特异性抗体VE1)进行盲观。抗体检测存在BRAF V600E突变的敏感性为97%(37/38),特异性为98%(58/59)。在发生BRAF基因突变的病例中,非V600E突变的病例中(包括V600K)无一例该抗体标记阳性(0/11)。5例BRAF基因突变结果不一致。加做分子学分析证实了3例免疫组织化学技术所得的BRAF结果,提示最初的分子学检测结果是错误的。2例患者在最初假阴性突变检测结果的基础上将不会接受BRAF抑制剂治疗。2例检测结果仍然不一致。所报道的IHC是对黑色素瘤患者V600E BRAF突变检测的一种准确、快速、经济的方法。临床V600E BRAF抗体的应用可以作为常规突变检测的一种有益补充,并且使得发生V600E突变的转移性黑色素瘤患者迅速分类进入适当的治疗途径。
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