Nakaji Yu, Oki Eiji, Nakanishi Ryota, Ando Koji, Sugiyama Masahiko, Nakashima Yuichiro, Yamashita Nami, Saeki Hiroshi, Oda Yoshinao, Maehara Yoshihiko
Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1, Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
J Cancer Res Clin Oncol. 2017 Jan;143(1):151-160. doi: 10.1007/s00432-016-2275-4. Epub 2016 Sep 26.
In colorectal cancer (CRC), the BRAF V600E mutation is an important biomarker for poor prognosis, while high microsatellite instability (MSI-H) indicates good prognosis. Using a commercial BRAF V600E-specific antibody, we investigated the BRAF V600E mutation according to immunohistochemistry (IHC) and the MSI status in Japanese patients with CRC.
In this retrospective study, tissue samples from 472 Japanese patients with CRC, stratified for MSI, were analyzed to determine the prognostic value of BRAF V600E, as assessed using IHC. Mutations in 254 patients were evaluated using the direct sequencing method to check for concordance.
The frequency of MSI-H was 9.3 % (44/472), and BRAF V600E mutation was detected immunohistochemically in 8.7 % patients (41/472). The sensitivity and specificity for detection of BRAF V600E mutations by IHC were 100 % (17/17) and 98.7 % (234/237), respectively. BRAF V600E mutations were significantly correlated with the anatomical tumor site (P = 0.0035), histological type (P < 0.0001), and MSI status (P < 0.0001). Consistent with other published series, patients with BRAF V600E mutation exhibited a significantly shorter overall survival (hazard ratio = 1.500, P = 0.0432). In particular, the microsatellite stable/BRAF mutation group had inferior prognosis compared with the MSI-H/BRAF wild-type group (hazard ratio = 2.621, P = 0.0004).
IHC using a BRAF V600E-specific antibody was useful for diagnosis and concurred with direct sequencing results. CRC cases could be stratified by combining BRAF V600E mutation and MSI status as a prognostic factor in Japanese patients.
在结直肠癌(CRC)中,BRAF V600E突变是预后不良的重要生物标志物,而高微卫星不稳定性(MSI-H)则提示预后良好。我们使用一种商业化的BRAF V600E特异性抗体,根据免疫组织化学(IHC)研究了日本CRC患者的BRAF V600E突变及MSI状态。
在这项回顾性研究中,对472例日本CRC患者按MSI分层的组织样本进行分析,以确定通过IHC评估的BRAF V600E的预后价值。使用直接测序法评估254例患者的突变情况以检查一致性。
MSI-H的频率为9.3%(44/472),免疫组织化学检测到BRAF V600E突变的患者为8.7%(41/472)。通过IHC检测BRAF V600E突变的敏感性和特异性分别为100%(17/17)和98.7%(234/237)。BRAF V600E突变与肿瘤解剖部位(P = 0.0035)、组织学类型(P < 0.0001)和MSI状态(P < 0.0001)显著相关。与其他已发表系列一致,BRAF V600E突变患者的总生存期显著缩短(风险比 = 1.500,P = 0.0432)。特别是,微卫星稳定/BRAF突变组的预后比MSI-H/BRAF野生型组差(风险比 = 2.621,P = 0.0004)。
使用BRAF V600E特异性抗体的IHC对诊断有用且与直接测序结果一致。在日本患者中,可将BRAF V600E突变和MSI状态结合作为预后因素对CRC病例进行分层。