Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Ann Surg Oncol. 2010 Apr;17(4):1033-42. doi: 10.1245/s10434-009-0854-1. Epub 2009 Dec 11.
Peritoneal relapse is the most common pattern of tumor progression in advanced gastric cancer. Clinicopathological findings are sometimes inadequate for predicting peritoneal relapse. The aim of this study was to identify patients at high risk of peritoneal relapse in a prospective study based on molecular prediction.
RNA samples from 141 primary gastric cancer tissues after curative surgery were profiled using oligonucleotide microarrays covering 30,000 human probes. Firstly, we constructed a molecular prediction system and validated its robustness and prognostic validity by 500 times multiple validation by repeated random sampling in a retrospective set of 56 (38 relapse-free and 18 peritoneal-relapse) patients. Secondly, we applied this prediction to 85 patients of the prospective set to assess predictive accuracy and prognostic validity.
In the retrospective phase, repeated random validation yielded approximately 68% predictive accuracy and a 22-gene expression profile associated with peritoneal relapse was identified. The prediction system identified patients with poor prognosis. In the prospective phase, the molecular prediction yielded 76.9% overall accuracy. Kaplan-Meier analysis of peritoneal-relapse-free survival showed a significant difference between the "good signature group" and "poor signature group" (log-rank p = 0.0017). Multivariate analysis by Cox regression hazards model identified the molecular prediction as the only independent prognostic factor for peritoneal relapse.
Gene expression profile inherent to primary gastric cancer tissues can be useful in prospective prediction of peritoneal relapse after curative surgery, potentially allowing individualized postoperative management to improve the prognosis of patients with advanced gastric cancer.
腹膜复发是晚期胃癌肿瘤进展最常见的模式。临床病理发现有时不足以预测腹膜复发。本研究的目的是在基于分子预测的前瞻性研究中确定腹膜复发高风险患者。
对 141 例根治性手术后的原发性胃癌组织的 RNA 样本进行了寡核苷酸微阵列分析,覆盖了 30000 个人类探针。首先,我们构建了一个分子预测系统,并通过在 56 例(38 例无复发生存和 18 例腹膜复发)患者的回顾性队列中进行 500 次重复随机抽样的多次验证来验证其稳健性和预后有效性。其次,我们将该预测应用于 85 例前瞻性队列患者,以评估预测准确性和预后有效性。
在回顾性阶段,重复随机验证得到了约 68%的预测准确性,并确定了与腹膜复发相关的 22 个基因表达谱。该预测系统识别出预后不良的患者。在前瞻性阶段,分子预测的总体准确率为 76.9%。腹膜无复发生存的 Kaplan-Meier 分析显示,“良好特征组”和“不良特征组”之间存在显著差异(对数秩检验 p = 0.0017)。Cox 回归风险模型的多变量分析确定了分子预测是腹膜复发的唯一独立预后因素。
原发性胃癌组织中固有的基因表达谱可用于预测根治性手术后的腹膜复发,可能允许进行个体化的术后管理,以改善晚期胃癌患者的预后。