Vuijk Floris A, van de Water Carlijn, Lent-van Vliet Shannon, van der Valk Maxime J M, Simmer Femke, van de Velde Cornelis J H, Vahrmeijer Alexander L, Nagtegaal Iris D, Hilling Denise E
Department of Surgery, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Department of Pathology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Cancers (Basel). 2021 May 9;13(9):2271. doi: 10.3390/cancers13092271.
Neoadjuvant therapy before surgical resection is indicated for patients with locally advanced rectal cancer. However, a significant number of patients show minimal or no response to neoadjuvant therapy. Unfortunately, we are currently unable to predict response and identify non-responding patients before neoadjuvant treatment is given. Genomic mutational status might provide valuable prognostic information. However, it is unclear whether predictions based on genomic mutational status in single preoperative biopsies are reliable due to intra-tumoral heterogeneity. In this study we aim to investigate the reliability of genomic mutations found in single pre-operative biopsies by comparing genomic mutations to four other locations within the same tumor using next generation sequencing. Rectal cancer patients undergoing primary resection without neoadjuvant therapy were included. From each patient, one biopsy, two deep and two superficial samples were obtained and sequenced using a targeted next generation sequencing gene panel. Concordance between these five samples was assessed. In this feasibility study we included 11 patients. In 7 out of 11 (64%) patients, all 5 samples showed concordant mutations. In 4 out of 11 patients (36%) discordant mutations were observed. In conclusion, assessment of mutational status on a single pre-operative biopsy shows discordance with tumor tissue from other locations in 36% of cases. These results warrant careful interpretation of biopsy material analysis, as these might be influenced by tumor heterogeneity.
对于局部晚期直肠癌患者,手术切除前需进行新辅助治疗。然而,相当一部分患者对新辅助治疗反应极小或无反应。不幸的是,目前我们无法在给予新辅助治疗前预测反应并识别无反应患者。基因组突变状态可能提供有价值的预后信息。然而,由于肿瘤内异质性,基于单次术前活检的基因组突变状态进行的预测是否可靠尚不清楚。在本研究中,我们旨在通过使用下一代测序将基因组突变与同一肿瘤内的其他四个位置进行比较,来研究单次术前活检中发现的基因组突变的可靠性。纳入了未接受新辅助治疗而进行初次切除的直肠癌患者。从每位患者获取一份活检样本、两份深部样本和两份浅表样本,并使用靶向下一代测序基因panel进行测序。评估这五个样本之间的一致性。在这项可行性研究中,我们纳入了11名患者。11名患者中有7名(64%),所有5个样本均显示一致的突变。11名患者中有4名(36%)观察到不一致的突变。总之,对单次术前活检的突变状态评估显示,36%的病例中与其他位置的肿瘤组织存在不一致。这些结果需要对活检材料分析进行谨慎解读,因为这些可能会受到肿瘤异质性的影响。