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Article type: Research Article
Authors: Hong, Tingting | Shen, Di | Chen, Xiaoping | Wu, Xiaohong | Hua, Dong*
Affiliations: Department of Medical Oncology, The Affiliated Hospital of Jiangnan University, Wuxi 4th People's Hospital, Wuxi 214062, Jiangsu, China
Correspondence: [*] Corresponding author: Dong Hua, Department of Medical Oncology, The Affiliated Hospital of Jiangnan University, Wuxi 4th People's Hospital, Huihe Road 200, Wuxi 214062, Jiangsu, China. Tel.: +86 051088682208; E-mail:[email protected]
Abstract: BACKGROUNDS: Cancer progression has been associated with host hemostasis system. Whether preoperative plasma hemostasis factors can predict survival in colorectal cancer is quite intriguing. METHODS: We conducted a prospective cohort study to validate the prognostic significance of three hemostasis parameters - fibrinogen, fibrin degradation products (FDPs) and D-dimer - in non-metastatic colorectal cancer patients treated with curative resection. RESULTS: All three parameters were positively correlated with C reactive protein (CRP) levels and Glasgow Prognostic scores (GPS). In univariate cox hazards regression model, as continuous variables, both fibrinogen (HR: 1.07, 95%CI: 1.01-1.13) and FDPs (HR: 1.17, 95%CI: 1.05-1.31) were prognostic, while D-dimer levels were not. Patients with hyperfibrinogenemia had a 2.12-fold increased mortality risk compared with patients without hyperfibrinogenemia. Patients with positive FDPs had a 3.68-fold increased mortality risk compared with patients with negative FDPs. In multivariate models, hyperfibrinogenemia was prognostic (HR: 3.39, 95%CI: 1.34-8.67) in patients with normal GPS scores. CONCLUSIONS: Preoperative fibrinogen levels appeared as an independent mortality risk factor in non-metastatic colorectal cancer patients with normal GPS scores. Fibrinogen could be a reliable marker to identify high risk patients for those without systematic inflammation responses.
Keywords: Colorectal neoplasms, survival, fibrinogen, fibrin/fibrinogen degradation products
DOI: 10.3233/CBM-160510
Journal: Cancer Biomarkers, vol. 19, no. 1, pp. 103-111, 2017
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