Huang Ming-Yii, Liu Hsueh-Chiao, Yen Li-Chen, Chang Jia-Yuan, Huang Jian-Jhang, Wang Jaw-Yuan, Hsiao Chao-Peng, Lin Shiu-Ru
Cancer Center, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan.
J Transl Med. 2014 May 26;12:147. doi: 10.1186/1479-5876-12-147.
The KRAS oncogene was one of the earliest discoveries of genetic alterations in colorectal and lung cancers. Moreover, KRAS somatic mutations might be used for predicting the efficiency of anti-EGFR therapeutic drugs. The purpose of this research was to improve Activating KRAS Detection Chip by using a weighted enzymatic chip array (WEnCA) platform to detect activated KRAS mutations status in the peripheral blood of non-small-cell lung cancer (NSCLC) and colorectal cancer (CRC) patients in Taiwan.
Our laboratory developed an Activating KRAS Detection Chip and a WEnCA technique that can detect activated KRAS mutation status by screening circulating cancer cells in the surrounding bloodstream. We collected 390 peripheral blood samples of NSCLC patients (n = 210) and CRC patients (n = 180) to evaluate clinical KRAS activation using this gene array diagnosis apparatus, an Activating KRAS Detection Chip and a WEnCA technique. Subsequently, we prospectively enrolled 88 stage III CRC patients who received adjuvant FOLFOX-4 chemotherapy with or without cetuximab. We compared the chip results of preoperative blood specimens and their relationship with disease control status in these patients.
After statistical analysis, the sensitivity of WEnCA was found to be 93%, and the specificity was found to be 94%. Relapse status and chip results among the stage III CRC patients receiving FOLFOX-4 plus cetuximab (n = 59) and those receiving FOLFOX-4 alone (n = 29) were compared. Among the 51 stage III CRC patients with chip negative results who were treated with FOLFOX-4 plus cetuximab chemotherapy, the relapse rate was 33.3%; otherwise, the relapse rate was 48.5% among the 23 out of 88 patients with chip negative results who received FOLFOX-4 alone. Negative chip results were significantly associated to better treatment outcomes in the FOLFOX-4 plus cetuximab group (P = 0.047).
The results demonstrated that the WEnCA technique is a sensitive and convenient technique that produces easy-to-interpret results for detecting activated KRAS from the peripheral blood of cancer patients. We suggest that the WEnCA technique is also a potential tool for predicting responses in CRC patients following FOLFOX-4 plus cetuximab chemotherapy.
KRAS癌基因是结直肠癌和肺癌中最早发现的基因改变之一。此外,KRAS体细胞突变可用于预测抗表皮生长因子受体(EGFR)治疗药物的疗效。本研究的目的是通过使用加权酶芯片阵列(WEnCA)平台改进激活型KRAS检测芯片,以检测台湾非小细胞肺癌(NSCLC)和结直肠癌(CRC)患者外周血中激活型KRAS突变状态。
我们实验室开发了一种激活型KRAS检测芯片和一种WEnCA技术,可通过筛查周围血流中的循环癌细胞来检测激活型KRAS突变状态。我们收集了390份NSCLC患者(n = 210)和CRC患者(n = 180)的外周血样本,使用这种基因阵列诊断设备、激活型KRAS检测芯片和WEnCA技术评估临床KRAS激活情况。随后,我们前瞻性纳入了88例接受含或不含西妥昔单抗的辅助FOLFOX - 4化疗的III期CRC患者。我们比较了术前血液标本的芯片结果及其与这些患者疾病控制状态的关系。
经过统计分析,发现WEnCA的敏感性为93%,特异性为94%。比较了接受FOLFOX - 4加西妥昔单抗(n = 59)和单独接受FOLFOX - 4(n = 29)的III期CRC患者的复发状态和芯片结果。在51例接受FOLFOX - 4加西妥昔单抗化疗且芯片结果为阴性的III期CRC患者中,复发率为33.3%;否则,在88例芯片结果为阴性且单独接受FOLFOX - 4的患者中,23例的复发率为48.5%。在FOLFOX - 4加西妥昔单抗组中芯片结果为阴性与更好的治疗结果显著相关(P = 0.047)。
结果表明,WEnCA技术是一种敏感且便捷的技术,能为从癌症患者外周血中检测激活型KRAS提供易于解读的结果。我们认为WEnCA技术也是预测CRC患者接受FOLFOX - 4加西妥昔单抗化疗反应的潜在工具。