Abstract
BackgroundThe purpose of this study was to build functional nomograms based on significant clinicopathological features to predict cause-specific survival (CSS) and overall survival (OS) in patients with stage I–III colon cancer.MethodsData on patients diagnosed with stage I–III colon cancer between 2010 and 2015 were downloaded from the Surveillance, Epidemiology, and End Results (SEER) database. Univariate and multivariate Cox analyses were used to identify independent prognostic factors, which were used to construct nomograms to predict the probabilities of CSS and OS. The performance of the nomogram was assessed by C-indexes, receiver operating characteristic (ROC) curves and calibration curves. Decision curve analysis (DCA) was used to compare clinical usage between the nomogram and the tumor–node–metastasis (TNM) staging system.ResultsBased on the univariate and multivariate analyses, features that correlated with survival outcomes were used to establish nomograms for CSS and OS prediction. The nomograms showed favorable sensitivity at predicting 1-, 3-, and 5-year CSS and OS, with a C-index of 0.78 (95% confidence interval (CI) 0.77–0.80) for CSS and 0.74 (95% CI 0.73–0.75) for OS. Calibration curves and ROC curves revealed excellent predictive accuracy. The clinically and statistically significant prognostic performance of the nomogram generated with the entire group of patients and risk scores was validated by a stratified analysis. DCA showed that the nomograms were more clinically useful than TNM stage.ConclusionNovel nomograms based on significant clinicopathological characteristics were developed and can be used as a tool for clinicians to predict CSS and OS in stage I–III colon cancer patients. These models could help facilitate a personalized postoperative evaluation.
Highlights
The purpose of this study was to build functional nomograms based on significant clinicopathological features to predict cause-specific survival (CSS) and overall survival (OS) in patients with stage I–III colon cancer
The prognosis of colon cancer is associated with the American Joint Commission on Cancer/International Union against Cancer (AJCC/UICC) tumor–node– metastasis (TNM) staging system
Eighteen variables were extracted from the SEER program in this study, including race, carcinoembryonic antigen (CEA) level, age, year of diagnosis, sex, adjuvant chemotherapy, histological type, grade, tumor size, number of lymph nodes harvested (LNH), regional nodes positive, LODDS stage, marital status, tumor site, tumor deposit, T stage, N stage, Fig. 1 The workflow of establishment of nomograms to predict cause-specific survival and overall survival of patients with stage I–III colon cancer and TNM stage
Summary
The purpose of this study was to build functional nomograms based on significant clinicopathological features to predict cause-specific survival (CSS) and overall survival (OS) in patients with stage I–III colon cancer. Patients with colon cancer had a 5-year OS rate of 65.2%, Zhou et al Cancer Cell Int (2019) 19:355 which made colon cancer a serious problem for public health. The prognosis of colon cancer is associated with the American Joint Commission on Cancer/International Union against Cancer (AJCC/UICC) tumor–node– metastasis (TNM) staging system. According to stages defined by the TNM system, the 5-year stage-specific survival rates are 93.2% for stage I, 82.5% for stage II, and 59.5% for stage III [3]. The TNM staging system is most widely used for prognosis assessment and medical treatments in colon cancer patients, excessive hidden defects still limit its practical application
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