Creation of a Novel Inflammation-Based Score for Operable Colorectal Cancer Patients

Qian Huang,1 Yinghao Cao,2 Shouyi Wang,1 Rui Zhu1 1Department of Pediatric, Zhongnan Hospital of Wuhan University, Wuhan, People’s Republic of China; 2Department of Colorectal Surgery and Gastroenterology, Wuhan Union Hospital, Tongji Medical College of Huazhong University of Science and T...

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Bibliographic Details
Main Authors: Huang Q, Cao Y, Wang S, Zhu R
Format: Article
Language:English
Published: Dove Medical Press 2020-10-01
Series:Journal of Inflammation Research
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Online Access:https://www.dovepress.com/creation-of-a-novel-inflammation-based-score-for-operable-colorectal-c-peer-reviewed-article-JIR
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Summary:Qian Huang,1 Yinghao Cao,2 Shouyi Wang,1 Rui Zhu1 1Department of Pediatric, Zhongnan Hospital of Wuhan University, Wuhan, People’s Republic of China; 2Department of Colorectal Surgery and Gastroenterology, Wuhan Union Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, People’s Republic of ChinaCorrespondence: Rui ZhuDepartment of Pediatric, Zhongnan Hospital of Wuhan University, No. 169 Donghu Road, Wuhan 430071, People’s Republic of ChinaEmail zhurui1226@126.comAim: Systemic inflammation has been implicated in the progression of patients with colorectal cancer (CRC). We evaluated the prognostic ability of a comprehensive score based on several inflammatory indexes in operable CRC patients.Patients and Methods: Between July 2013 and September 2017, this study retrospectively identified 1279 CRC patients receiving radical surgery in Wuhan Union Hospital and randomly assigned them into training (N=921) and validation (N=358) sets. A novel score, the CRC-specific inflammatory index (CSII), was developed from a series of inflammatory indexes significantly associated with survival in patients with CRC. This novel score was then divided into three categories and compared to the well-known systematic inflammatory index (SII) and TNM stage. Finally, a survival nomogram was generated by combining the CSII and other informative clinical features.Results: The CSII-OS was calculated as 1.110×lg ALRI + 1.082×CAR + 0.792×PI, while CSII-DFS was 1.709×lg ALRI + 1.033×CAR based on multivariable Cox regression analysis. Patients with high CSII experienced a worse OS (HR=23.72, 95% CI, 11.30– 49.78, P < 0.001) and worse DFS (HR=15.62, 95% CI, 6.95– 35.08, P < 0.001) compared to those in CRC patients with low CSII. Moreover, ROC analyses showed that the CSII possessed excellent performance (AUC=0.859) in predicting OS and DFS. The AUC of the OS nomogram based on CSII, TNM stage, and chemotherapy was 0.897, while that of the DFS nomogram based on CSII, T stage, and TNM stage was 0.873. High-quality calibration curves in both OS and DFS nomograms were observed. Verification in the validation dataset showed results consistent with those in the training dataset.Conclusion: The CSII is a CRC-specific prognostic score based on the combination of available inflammatory indexes. High CSII is a strong predictor of worse survival outcomes. The CSII also exhibits better predictive performance compared to SII or TNM stage in operable CRC patients.Keywords: colorectal cancer, systemic inflammation, prognosis, CRC-specific inflammatory index, survival nomogram
ISSN:1178-7031