Abstract

BackgroundWe initially proposed a useful and novel prognostic model, named CCS [Combination of c-reactive protein (CRP) and squamous cell carcinoma antigen (SCC)], for predicting the postoperative survival in patients with esophageal squamous cell carcinoma (ESCC).MethodsTwo hundred and fifty-two patients with resectable ESCC were included in this retrospective study. A logistic regression was performed and yielded a logistic equation. The CCS was calculated by the combined CRP and SCC. The optimal cut-off value for CCS was evaluated by X-tile program. Univariate and multivariate analyses were used to evaluate the predictive factors. In addition, a novel nomogram model was also performed to predict the prognosis for patients with ESCC.ResultsIn the current study, CCS was calculated as CRP+6.33 SCC according to the logistic equation. The optimal cut-off value was 15.8 for CCS according to the X-tile program. Kaplan-Meier analyses demonstrated that high CCS group had a significantly poor 5-year cancer-specific survival (CSS) than low CCS group (10.3% vs. 47.3%, P <0.001). According to multivariate analyses, CCS (P =0.004), but not CRP (P =0.466) or SCC (P =0.926), was an independent prognostic factor. A nomogram could be more accuracy for CSS (Harrell's c-index: 0.70).ConclusionThe CCS is a usefull and independent predictive factor in patients with ESCC.

Highlights

  • Esophageal cancer (EC) is one of the most fatal types of cancer, leading to over 406,800 deaths worldwide and more than 200,000 deaths in China annually [1, 2]

  • In the current study, CCS was calculated as c-reactive protein (CRP)+6.33 squamous cell carcinoma antigen (SCC) according to the logistic equation

  • The optimal cut-off value was 15.8 for CCS according to the X-tile program

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Summary

Introduction

Esophageal cancer (EC) is one of the most fatal types of cancer, leading to over 406,800 deaths worldwide and more than 200,000 deaths in China annually [1, 2]. Esophageal squamous cell carcinoma (ESCC) is the predominant pathological type in China, which covers more than 90% of all EC cases [3, 4]. Serum c-reactive protein (CRP) is a sensitive biomarker for inflammation. Recent studies revealed that CRP was associated with prognosis in several cancers [810]. The prognostic role of CRP in EC is still controversial [11,12,13,14]. We initially proposed a useful and novel prognostic model, named CCS [Combination of c-reactive protein (CRP) and squamous cell carcinoma antigen (SCC)], for predicting the postoperative survival in patients with esophageal squamous cell carcinoma (ESCC)

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