A Nomogram for Predicting the Cancer-Specific Survival of Patients with Initially Diagnosed Metastatic Gastric Cancer

被引:0
作者
Ren, Jun [1 ,2 ]
Dai, Yuedi [3 ]
Chao, Fei [4 ]
Tang, Dong [2 ]
Gu, Jiawei [1 ]
Niu, Gengming [1 ]
Xia, Jie [1 ]
Wang, Xin [1 ]
Song, Tao [1 ]
Hu, Zhiqing [1 ]
Hong, Runqi [1 ]
Ke, Chongwei [1 ,5 ]
机构
[1] Fudan Univ, Shanghai Peoples Hosp 5, Dept Gen Surg, Shanghai, Peoples R China
[2] Yangzhou Univ, Northern Jiangsu Peoples Hosp, Clin Med Sch, Dept Gen Surg, Yangzhou, Peoples R China
[3] Fudan Univ, Dept Med Oncol, Minhang Branch, Shanghai Canc Ctr, Shanghai, Peoples R China
[4] Yangzhou Univ, Northern Jiangsu Peoples Hosp, Clin Med Sch, Dept Anesthesiol, Yangzhou, Peoples R China
[5] Fudan Univ, Shanghai Peoples Hosp 5, Dept Gen Surg, 801 Heqing Rd, Shanghai 200240, Peoples R China
关键词
Metastatic gastric cancer; prognostic model; nomogram; cancer-specific survival; chemotherapy;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background:There are few models to predict the survival of patients of different ethnicities initially diagnosed with metastatic gastric cancer (mGC). Therefore, the aim of this study was to construct a nomogram to predict the cancer-specific survival (CSS) of these patients. Methods:Data for 994 patients initially diagnosed with mGC between 2000 and 2013 were extracted from the Surveillance, Epidemiology, and End Results database. Patients were randomly classified into a training (n = 696) or internal validation (n = 298) cohort, and a cohort of 133 patients from Fudan cohort was used for external validation. A nomogram to predict the CSS of mGC patients was derived and validated using a concordance index (C-index), calibration curves, and decision-curve analysis (DCA). Results:Multivariate Cox regression indicated that five factors were independent predictors of CSS: differentiation grade, T stage, N stage, metastatic site at diagnosis, and with or without chemotherapy. Thus, these factors were integrated into the nomogram model. The C-index value of the nomogram model was 0.63 (95% CI: 0.60-0.65), and those of the internal and external validation cohorts were 0.60 (95%: CI 0.55-0.64) and 0.63 (95%: CI 0.57-0.69), respectively. The calibration curves showed good consistency between the actual and predicted survival rates in both the internal and external validation cohorts. The DCA also showed the clinical utility of the nomogram model. Conclusions:We established a practical nomogram to predict the CSS of patients initially diagnosed with mGC. The nomogram can be used for individualized prediction of survival and to guide clinicians in making treatment decisions.
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页数:9
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