Vogelaar F Jeroen, Erning Felice N van, Reimers Marlies S, Linden Hans van der, Pruijt Hans, Brule Adriaan J C van den, Bosscha Koop
Department of Surgery, Jeroen Bosch Hospital, The Netherlands.
Department of Surgery, VieCuri Medical Center, The Netherlands.
Mol Med. 2016 May;21(1):1038-1046. doi: 10.2119/molmed.2015.00220. Epub 2016 May 9.
In the era of personalized cancer medicine, identifying mutations within patient tumors plays an important role in defining high-risk stage II colon cancer patients. The prognostic role of V600E mutation, microsatellite instability (MSI) status, mutation and mutation in stage II colon cancer patients is not settled. We retrospectively analyzed 186 patients with stage II colon cancer who underwent an oncological resection but were not treated with adjuvant chemotherapy. mutations, mutation, V600E mutation and MSI status were determined. Survival analyses were performed. Mutations were found in the patients with each mutation in the following percentages: 23% (MSI), 35% (), 19% () and 11% (). A trend toward worse overall survival (OS) was seen in patients with an MSI (5-year OS 74% versus 82%, adjusted hazard ratio [HR] 1.8, 95% confidence interval [CI] 0.6-4.9) and a -mutated tumor (5-year OS 77% versus 82%, adjusted HR 1.7, 95% CI 0.8-3.5). MSI and -mutated tumors tended to correlate with poorer disease-free survival (DFS) (5-year DFS 60% versus 78%, adjusted HR 1.6, 95% CI 0.5-2.1 and 5-year DFS 57% versus 77%, adjusted HR 1.1, 95% CI 0.4-2.6 respectively). In stage II colon cancer patients not treated with adjuvant chemotherapy, mutation and MSI status both tended to have a negative prognostic effect on disease-free survival. and MSI status also tended to be correlated with worse overall survival.
在个性化癌症医学时代,识别患者肿瘤内的突变对于界定高危II期结肠癌患者起着重要作用。V600E突变、微卫星不稳定性(MSI)状态、[此处原文缺失两个基因名称]突变在II期结肠癌患者中的预后作用尚未明确。我们回顾性分析了186例接受肿瘤切除但未接受辅助化疗的II期结肠癌患者。确定了[此处原文缺失两个基因名称]突变、[此处原文缺失两个基因名称]突变、V600E突变和MSI状态,并进行了生存分析。发现每种突变的患者中存在突变的比例如下:23%(MSI)、35%([此处原文缺失两个基因名称])、19%([此处原文缺失两个基因名称])和11%(V600E)。MSI患者(5年总生存率[OS]为74%,而未发生MSI者为82%,调整后风险比[HR]为1.8,95%置信区间[CI]为0.6 - 4.9)和发生[此处原文缺失两个基因名称]突变肿瘤的患者(5年OS为77%,而未发生者为82%,调整后HR为1.7,95%CI为0.8 - 3.5)总体生存呈现出较差的趋势。MSI和[此处原文缺失两个基因名称]突变肿瘤往往与较差的无病生存率(DFS)相关(5年DFS分别为60%和78%,调整后HR为1.6,95%CI为0.5 - 2.1;以及5年DFS分别为57%和77%,调整后HR为1.1,95%CI为0.4 - 2.6)。在未接受辅助化疗的II期结肠癌患者中,[此处原文缺失两个基因名称]突变和MSI状态对无病生存均倾向于具有负面预后影响。[此处原文缺失两个基因名称]和MSI状态也往往与较差的总体生存相关。