Sun Ke, Xu Meng Qing, Zhang Hai Jun, Zhang Dan Dan, Yue Wen, Ma Miao Miao, Tao Lin, Zhang Wen Jie
Department of Pathology, The First Affiliated Hospital, School of Medicine, Shihezi University Shihezi 832002, Xinjiang, China.
Key Laboratory for Xinjiang Endemic and Ethnic Diseases, School of Medicine, Shihezi University Shihezi 832002, Xinjiang, China.
Am J Transl Res. 2022 Apr 15;14(4):2317-2330. eCollection 2022.
TNM staging of gastric cancer (GC) is useful in predicting prognosis, but its definition is only possible after surgery. It is therefore desirable to develop a method that can predict prognosis and assist management options before surgery.
This study investigated 110 GC patients after radical gastrectomy and followed-up for 136 months. Patients' complete clinicopathological data were collected and gastroscopically biopsied or surgically resected tissues were examined for the expression of Her-2, nm-23, CEA and phosphorylated Stat3 (p-Stat3) using immunohistochemistry (IHC). Univariate and multivariate ROC curves, Kaplan-Meier survival curves, and SPSS Version 22.0 and R (version 3.6.1) statistical software were used to analyze the data.
Three major findings were observed: (1) Tissue levels of p-Stat3, Her-2, CEA and nm-23 were correlated with GC patients' survival probability termed as survival prediction power (SPP). (2) Using 5-year survival as an end-point, the SPP of the p-Stat3+Her-2 combination was stronger (AUC=0.867) than that of TNM staging (AUC=0.755). (3) Using cut-off values derived from ROC curves, Kaplan-Meier analyses showed that the p-Stat3+Her-2 molecular combination could clearly predict overall survival rates between the predictive low-risk patients (69.2%) and the predictive high-risk patients (13.2%) with a discriminative difference as high as 56.0%.
We conclude that area under the ROC curve (AUC) can be used to quantify SPP powers for biomarkers, making cross-comparisons possible among different survival predictors. This study has first established a multi-factor survival prediction model by which the p-Stat3+Her-2 combination has the best discriminative capability to differentiate low-risk patients from high-risk patients in terms of survival prognosis.
胃癌(GC)的TNM分期有助于预测预后,但其定义只能在手术后确定。因此,需要开发一种能够在手术前预测预后并辅助管理方案的方法。
本研究对110例行根治性胃切除术的GC患者进行了136个月的随访。收集患者完整的临床病理数据,并通过免疫组织化学(IHC)检测胃镜活检或手术切除组织中Her-2、nm-23、CEA和磷酸化Stat3(p-Stat3)的表达。使用单变量和多变量ROC曲线、Kaplan-Meier生存曲线以及SPSS 22.0版和R(3.6.1版)统计软件进行数据分析。
观察到三个主要发现:(1)p-Stat3、Her-2、CEA和nm-23的组织水平与GC患者的生存概率相关,称为生存预测能力(SPP)。(2)以5年生存率为终点,p-Stat3+Her-2组合的SPP(AUC=0.867)强于TNM分期(AUC=0.755)。(3)使用ROC曲线得出的临界值,Kaplan-Meier分析表明,p-Stat3+Her-2分子组合能够清晰地预测预测低风险患者(69.2%)和预测高风险患者(13.2%)之间的总生存率,判别差异高达56.0%。
我们得出结论,ROC曲线下面积(AUC)可用于量化生物标志物的SPP能力,从而使不同生存预测指标之间的交叉比较成为可能。本研究首次建立了多因素生存预测模型,其中p-Stat3+Her-2组合在生存预后方面区分低风险患者和高风险患者的判别能力最佳。