Kadowaki Shigenori, Kakuta Miho, Takahashi Shuhei, Takahashi Akemi, Arai Yoshiko, Nishimura Yoji, Yatsuoka Toshimasa, Ooki Akira, Yamaguchi Kensei, Matsuo Keitaro, Muro Kei, Akagi Kiwamu
Shigenori Kadowaki, Akira Ooki, Kensei Yamaguchi, Division of Gastroenterology, Saitama Cancer Center, Saitama 362-0806, Japan.
World J Gastroenterol. 2015 Jan 28;21(4):1275-83. doi: 10.3748/wjg.v21.i4.1275.
To investigate the prognostic role of KRAS and BRAF mutations after adjustment for microsatellite instability (MSI) status in Japanese colorectal cancer (CRC) population.
We assessed KRAS and BRAF mutations and MSI status in 813 Japanese patients with curatively resected, stage I-III CRC and examined associations of these mutations with disease-free survival (DFS) and overall survival (OS) using uni- and multivariate Cox proportional hazards models.
KRAS and BRAF mutations were detected in 312 (38%) of 812 and 40 (5%) of 811 tumors, respectively. KRAS mutations occurred more frequently in females than in males (P=0.02), while the presence of BRAF mutations was significantly associated with the female gender (P=0.006), proximal tumor location (P<0.001), mucinous or poorly differentiated histology (P<0.001), and MSI-high tumors (P<0.001). After adjusting for relevant variables, including MSI status, KRAS mutations were associated with poorer DFS (HR=1.35; 95%CI: 1.03-1.75) and OS (HR=1.46; 95%CI: 1.09-1.97). BRAF mutations were poor prognostic factors for DFS (HR=2.20; 95%CI: 1.19-4.06) and OS (HR=2.30; 95%CI: 1.15-4.71). Neither the BRAF by MSI interaction test nor the KRAS by MSI interaction test yielded statistically significant results for DFS and OS.
KRAS and BRAF mutations are associated with inferior survival, independent of MSI status, in Japanese patients with curatively resected CRC.
在日本结直肠癌(CRC)人群中,研究校正微卫星不稳定性(MSI)状态后KRAS和BRAF突变的预后作用。
我们评估了813例接受根治性切除的Ⅰ-Ⅲ期日本CRC患者的KRAS和BRAF突变以及MSI状态,并使用单因素和多因素Cox比例风险模型检查这些突变与无病生存期(DFS)和总生存期(OS)的相关性。
在812例肿瘤中的312例(38%)和811例肿瘤中的40例(5%)中分别检测到KRAS和BRAF突变。KRAS突变在女性中比在男性中更频繁发生(P=0.02),而BRAF突变的存在与女性性别(P=0.006)、肿瘤近端位置(P<0.001)、黏液性或低分化组织学(P<0.001)以及MSI高的肿瘤(P<0.001)显著相关。在校正包括MSI状态在内的相关变量后,KRAS突变与较差的DFS(HR=1.35;95%CI:1.03-1.75)和OS(HR=1.46;95%CI:1.09-1.97)相关。BRAF突变是DFS(HR=2.20;95%CI:1.19-4.06)和OS(HR=2.30;95%CI:1.15-4.71)的不良预后因素。BRAF与MSI的相互作用试验以及KRAS与MSI的相互作用试验在DFS和OS方面均未产生具有统计学意义的结果。
在接受根治性切除的日本CRC患者中,KRAS和BRAF突变与较差的生存率相关,且与MSI状态无关。