Liersch Torsten, Grade Marian, Gaedcke Jochen, Varma Sudhir, Difilippantonio Michael J, Langer Claus, Hess Clemens F, Becker Heinz, Ried Thomas, Ghadimi B Michael
Department of General and Visceral Surgery, University Medical Center, Georg-August-University, Robert Koch Str. 40, 37075 Göttingen, Germany.
Cancer Genet Cytogenet. 2009 Apr 15;190(2):57-65. doi: 10.1016/j.cancergencyto.2008.11.011.
Preoperative chemoradiotherapy is recommended for locally advanced rectal cancer (UICC stage II/III). We recently demonstrated that responsive and nonresponsive tumors showed differential expression levels of 54 genes. In this follow-up study, we investigated the relationship between this gene set and disease-free (DFS) and overall survival (OS). Pretherapeutic biopsies from 30 participants in the CAO/ARO/AIO-94 trial of the German Rectal Cancer Study Group were analyzed using gene expression microarrays. Statistical analysis was performed to identify differentially expressed genes between recurrent and nonrecurrent tumors and to correlate these changes with disease recurrence and outcome. After a median follow-up of 59 months, seven of eight patients with recurrent disease was a nonresponder, and one responsive tumor recurred. Response to chemoradiotherapy was significantly correlated with an improved DFS (log rank P=0.028), whereas OS did not differ significantly (P=0.11). Applying a class comparison analysis, we identified 20 genes that were differentially expressed between recurrent and nonrecurrent tumors (P<0.001). Analyzing the first two principal components of the 54 genes previously identified to predict response, we observed that this response signature correlated with an increased risk of cancer recurrence. These data suggest that the genetic basis of local response also affects the genetic basis of tumor recurrence. Genes that are indicative of nonresponse to preoperative chemoradiotherapy might also be linked to an increased risk of tumor recurrence.
对于局部晚期直肠癌(UICC II/III期),推荐进行术前放化疗。我们最近发现,反应性和无反应性肿瘤的54个基因表达水平存在差异。在这项随访研究中,我们调查了这个基因集与无病生存期(DFS)和总生存期(OS)之间的关系。使用基因表达微阵列分析了德国直肠癌研究组CAO/ARO/AIO-94试验中30名参与者的治疗前活检样本。进行统计分析以确定复发肿瘤和未复发肿瘤之间的差异表达基因,并将这些变化与疾病复发和预后相关联。中位随访59个月后,8例复发疾病患者中有7例为无反应者,1例反应性肿瘤复发。对放化疗的反应与改善的DFS显著相关(对数秩检验P = 0.028),而OS无显著差异(P = 0.11)。应用类比较分析,我们确定了20个在复发肿瘤和未复发肿瘤之间差异表达的基因(P < 0.001)。分析先前确定的用于预测反应的54个基因的前两个主成分,我们观察到这种反应特征与癌症复发风险增加相关。这些数据表明,局部反应的遗传基础也影响肿瘤复发的遗传基础。提示对术前放化疗无反应的基因也可能与肿瘤复发风险增加有关。