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Asian Pac J Cancer Prev. 2019 Oct 1;20(10):2979-2985. doi: 10.31557/APJCP.2019.20.10.2979.
2
Estimating the global cancer incidence and mortality in 2018: GLOBOCAN sources and methods.估算 2018 年全球癌症发病率和死亡率:GLOBOCAN 来源和方法。
Int J Cancer. 2019 Apr 15;144(8):1941-1953. doi: 10.1002/ijc.31937. Epub 2018 Dec 6.
3
The prognosis role of AJCC/UICC 8 edition staging system in gastric cancer, a retrospective analysis.AJCC/UICC第8版分期系统在胃癌中的预后作用:一项回顾性分析
Am J Transl Res. 2018 Jan 15;10(1):292-303. eCollection 2018.
4
Global surveillance of trends in cancer survival 2000-14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries.全球癌症生存趋势监测 2000-14 年(CONCORD-3):对来自 71 个国家 322 个基于人群的登记处的 37513025 名诊断患有 18 种癌症之一的患者的个体记录进行分析。
Lancet. 2018 Mar 17;391(10125):1023-1075. doi: 10.1016/S0140-6736(17)33326-3. Epub 2018 Jan 31.
5
Preoperative Body Mass Index, Blood Albumin and Triglycerides Predict Survival for Patients with Gastric Cancer.术前体重指数、血白蛋白和甘油三酯可预测胃癌患者的生存率。
PLoS One. 2016 Jun 16;11(6):e0157401. doi: 10.1371/journal.pone.0157401. eCollection 2016.
6
Overexpression of STAT3/pSTAT3 was associated with poor prognosis in gastric cancer: a meta-analysis.STAT3/pSTAT3过表达与胃癌预后不良相关:一项荟萃分析。
Int J Clin Exp Med. 2015 Nov 15;8(11):20014-23. eCollection 2015.
7
Cancer statistics in China, 2015.《中国癌症统计数据 2015》
CA Cancer J Clin. 2016 Mar-Apr;66(2):115-32. doi: 10.3322/caac.21338. Epub 2016 Jan 25.
8
Preoperative C-Reactive Protein/Albumin Ratio Predicts Prognosis of Patients after Curative Resection for Gastric Cancer.术前C反应蛋白/白蛋白比值可预测胃癌根治性切除术后患者的预后。
Transl Oncol. 2015 Aug;8(4):339-45. doi: 10.1016/j.tranon.2015.06.006.
9
Human papillomavirus infection correlates with inflammatory Stat3 signaling activity and IL-17 level in patients with colorectal cancer.人乳头瘤病毒感染与结直肠癌患者炎症性Stat3信号传导活性及IL-17水平相关。
PLoS One. 2015 Feb 23;10(2):e0118391. doi: 10.1371/journal.pone.0118391. eCollection 2015.
10
The distinctive nature of HER2-positive gastric cancers.HER2 阳性胃癌的独特性质。
Eur J Surg Oncol. 2015 Mar;41(3):271-3. doi: 10.1016/j.ejso.2014.12.007. Epub 2015 Jan 10.

作为联合生存预测指标的活性Stat3和Her-2对胃癌术后患者显示出优于TNM分期系统的优势。

Active Stat3 and Her-2 as combined survival predictors show superiority to TNM staging system for postoperative patients with gastric cancer.

作者信息

Sun Ke, Xu Meng Qing, Zhang Hai Jun, Zhang Dan Dan, Yue Wen, Ma Miao Miao, Tao Lin, Zhang Wen Jie

机构信息

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.

出版信息

Am J Transl Res. 2022 Apr 15;14(4):2317-2330. eCollection 2022.

PMID:35559376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9091078/
Abstract

OBJECTIVES

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.

METHODS

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.

RESULTS

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%.

CONCLUSIONS

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.

摘要

目的

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。

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。

结果

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%。

结论

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。