Prognostic Nomograms for Predicting Overall Survival and Cancer-Specific Survival of Patients With Early Onset Colon Adenocarcinoma

被引:7
|
作者
Jin, Huimin [1 ]
Feng, Yuqian [1 ]
Guo, Kaibo [1 ]
Ruan, Shanming [2 ]
机构
[1] Zhejiang Chinese Med Univ, Clin Med Coll 1, Hangzhou, Peoples R China
[2] Zhejiang Chinese Med Univ, Affiliated Hosp 1, Dept Med Oncol, Hangzhou, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2020年 / 10卷
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
nomogram; overall survival; cancer-specific survival; early onset colon adenocarcinoma; prognosis; Surveillance; Epidemiology and End Results database; RECURRENCE;
D O I
10.3389/fonc.2020.595354
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The incidence of colon cancer in young patients is on the rise, of which adenocarcinoma is the most common pathological type. However, a reliable nomogram for early onset colon adenocarcinoma (EOCA) to predict prognosis is currently lacking. This study aims to develop nomograms for predicting the overall survival (OS) and cancer-specific survival (CSS) of patients with EOCA. Methods Patients diagnosed with EOCA from 2010 to 2015 were included and randomly assigned to training set and validation set. Cox regression models were used to evaluate prognosis and identify independent predictive factors, which were then utilized to establish the nomograms for predicting 3- and 5-year OS and CSS. The discrimination and calibration of nomograms were validated using the calibration plots, concordance index, receiver operating characteristics curve, and the decision curve analysis. Results A total of 2,348 patients were screened out, with 1,644 categorized into the training set and 704 into the validation set. Multivariate analysis demonstrated that gender, age, tumor size, T stage, M stage, regional node, tumor deposits, lung metastasis and perineural invasion were significantly correlated with OS and CSS. The calibration plots indicated that there was good consistency between the nomogram prediction and actual observation. The C-indices for training set of OS and CSS prediction nomograms were 0.735 (95% CI: 0.708-0.762) and 0.765 (95% CI: 0.739-0.791), respectively, whereas those for validation set were 0.736 (95% CI: 0.696-0.776) and 0.76 (95% CI: 0.722-0.798), respectively. The results of ROC analysis revealed the nomograms showed a good discriminate power. The 3- and 5-year DCA curves displayed superiority over TNM staging system with higher net benefit gains. Conclusions The nomograms established could effectively predict 3- and 5-year OS and CSS in EOCA patients, which assisted clinicians to evaluate prognosis more accurately and optimize treatment strategies.
引用
收藏
页数:11
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