Development and Validation of a Nomogram to Predict Overall Survival in Stage I-III Colorectal Cancer Patients after Radical Resection with Normal Preoperative Serum Carcinoembryonic Antigen

被引:1
作者
Dai, Xuan [1 ]
Wang, Haoran [2 ]
Lu, Yaqi [2 ]
Chen, Yan [1 ]
Liu, Yun [1 ]
Huang, Shiyong [1 ]
机构
[1] Shanghai Jiao Tong Univ, Xinhua Hosp, Dept Colorectal & Anal Surg, Sch Med, Shanghai 200092, Peoples R China
[2] Xinxiang Med Univ, Clin Sch 1, Xinxiang 453003, Peoples R China
基金
中国国家自然科学基金;
关键词
colorectal cancer; nomogram; overall survival; CA242; CA125; CURATIVE RESECTION; FOLLOW-UP; CLINICAL-SIGNIFICANCE; PROGNOSTIC VALUE; CEA; RECURRENCE; CA125; CA19-9; COMBINATION; EXPRESSION;
D O I
10.3390/cancers15235643
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary A considerable number of patients with colorectal cancer (CRC) do not have elevated serum carcinoembryonic antigen (CEA) levels before undergoing radical surgery for colorectal cancer, but they may still have a poor prognosis. It is imperative to find sensitive and dependable prognostic markers to quickly identify high-risk populations who are susceptible to adverse outcomes in order to offer timely interventions to improve prognosis. In this real-world study of more than 1000 samples, a nomogram based on serum tumor markers and other clinicopathological features was used to accurately forecast the 3-year and 5-year overall survival rates of stage I-III CRC patients after radical resection with normal preoperative CEA, and its predictive power and clinical applicability markedly exceed those of the AJCC 8th TNM stage. In addition, we found the potential prognostic values of carbohydrate antigen 125 (CA125) and carbohydrate antigen 242 (CA242) as supplementary tumor markers in CRC patients who have normal preoperative CEA.Abstract We aimed to develop a clinical predictive model for predicting the overall survival (OS) in stage I-III CRC patients after radical resection with normal preoperative CEA. This study included 1082 consecutive patients. They were further divided into a training set (70%) and a validation set (30%). The selection of variables for the model was informed by the Akaike information criterion. After that, the clinical predictive model was constructed, evaluated, and validated. The net reclassification index (NRI) and integrated discrimination improvement (IDI) were employed to compare the models. Age, histologic type, pT stage, pN stage, carbohydrate antigen 242 (CA242), and carbohydrate antigen 125 (CA125) were selected to establish a clinical prediction model for OS. The concordance index (C-index) (0.748 for the training set and 0.702 for the validation set) indicated that the nomogram had good discrimination ability. The decision curve analysis highlighted that the model has superior efficiency in clinical decision-making. NRI and IDI showed that the established nomogram markedly outperformed the TNM stage. The new clinical prediction model was notably superior to the AJCC 8th TNM stage, and it can be used to accurately assess the OS of stage I-III CRC patients undergoing radical resection with normal preoperative CEA.
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页数:16
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