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一种突变型BRAF V600E特异性免疫组化检测:与结直肠癌分子突变状态及临床结局的相关性

A mutant BRAF V600E-specific immunohistochemical assay: correlation with molecular mutation status and clinical outcome in colorectal cancer.

作者信息

Day Fiona, Muranyi Andrea, Singh Shalini, Shanmugam Kandavel, Williams David, Byrne David, Pham Kym, Palmieri Michelle, Tie Jeanne, Grogan Thomas, Gibbs Peter, Sieber Oliver, Waring Paul, Desai Jayesh

机构信息

Ludwig Colon Cancer Initiative Laboratory, Ludwig Institute for Cancer Research, Parkville, VIC, Australia.

出版信息

Target Oncol. 2015 Mar;10(1):99-109. doi: 10.1007/s11523-014-0319-8. Epub 2014 May 27.

Abstract

The B-type Raf kinase (BRAF) V600E mutation is a well-established biomarker for poor prognosis in metastatic colorectal cancer (mCRC) and is a highly attractive drug target. A barrier to the development of new therapies targeting BRAF V600E in mCRC is the low prevalence of mutations (approximately 10 %) and the current need for access to sequencing-based technologies which are not routinely available outside of large cancer centres. Availability of a standardised immunohistochemistry (IHC) test, more suited to routine pathology practice, would provide much broader access to patient identification. We sought to evaluate the accuracy and clinical utility of a recently developed BRAF V600E IHC method as a prognostic biomarker in a large cohort of community-based CRC patients. Archival tumour samples from 505 patients with stage I-IV CRC were immunohistochemically tested with two antibodies, pBR1 for total BRAF and VE1 for BRAF V600E. Cases were assessed by two blinded pathologists, and results were compared to BRAF V600E mutation status determined using DNA sequencing. Discordant cases were retested with a BRAF V600E SNaPshot assay. BRAF mutation status was correlated with overall survival (OS) in stage IV CRC. By DNA sequencing and IHC, 505 and 477 patients were respectively evaluable. Out of 477 patients, 56 (11. 7 %) had BRAF V600E mutations detected by sequencing and 63 (13.2 %) by IHC. Using DNA sequencing results as the reference, sensitivity and specificity for IHC were 98.2 % (55/56) and 98.1 % (413/421), respectively. IHC had a positive predictive value (PPV) of 87.3 % (55/63) and a negative predictive value (NPV) of 99.8 % (413/414). Compared to DNA sequencing plus retesting of available discordant cases by SNaPshot assay, IHC using the VE1 antibody had a 100 % sensitivity (59/59), specificity (416/416), NPV (416/416) and PPV (59/59). Stage IV CRC patients with BRAF V600E protein detected by IHC exhibited a significantly shorter overall survival (hazard ratio = 2.20, 95 % CI 1.26-3.83, p = 0.005), consistent with other published series. Immunohistochemistry using the BRAF V600E VE1 antibody is an accurate diagnostic assay in CRC. The test provides a simple, clinically applicable method of testing for the BRAF V600E mutation in routine practice.

摘要

B型Raf激酶(BRAF)V600E突变是转移性结直肠癌(mCRC)预后不良的一个公认生物标志物,也是一个极具吸引力的药物靶点。在mCRC中,开发针对BRAF V600E的新疗法面临的一个障碍是突变发生率较低(约10%),且目前需要使用基于测序的技术,而这些技术在大型癌症中心之外并非常规可用。一种更适合常规病理实践的标准化免疫组织化学(IHC)检测方法的出现,将使更多患者能够进行该检测以确定是否存在BRAF V600E突变。我们试图评估一种最近开发的BRAF V600E IHC方法作为一大群社区CRC患者预后生物标志物的准确性和临床实用性。对505例I-IV期CRC患者的存档肿瘤样本进行免疫组织化学检测,使用两种抗体,针对总BRAF的pBR1和针对BRAF V600E的VE1。由两名盲法病理学家评估病例,并将结果与使用DNA测序确定的BRAF V600E突变状态进行比较。对不一致的病例用BRAF V600E SNaPshot分析法重新检测。BRAF突变状态与IV期CRC患者的总生存期(OS)相关。通过DNA测序和IHC分别可评估505例和477例患者。在477例患者中,测序检测到56例(11.7%)有BRAF V600E突变,IHC检测到63例(13.2%)。以DNA测序结果为参考,IHC的敏感性和特异性分别为98.2%(55/56)和98.1%(413/421)。IHC的阳性预测值(PPV)为87.3%(55/63),阴性预测值(NPV)为99.8%(413/414)。与DNA测序加对可用不一致病例进行SNaPshot分析法重新检测相比,使用VE1抗体的IHC敏感性为100%(59/59)、特异性为100%(416/416)、NPV为100%(416/416)、PPV为100%(59/59)。通过IHC检测到BRAF V600E蛋白的IV期CRC患者的总生存期显著缩短(风险比=2.20,95%CI 1.26-3.83,p=0.005),与其他已发表系列一致。使用BRAF V600E VE1抗体的免疫组织化学在CRC中是一种准确的诊断方法。该检测为常规实践中检测BRAF V600E突变提供了一种简单、临床适用的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/4363480/cd1fad1d9bc6/11523_2014_319_Fig1_HTML.jpg

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