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Colorectal Cancer, Systemic Inflammation, and Outcome

医学 四分位间距 内科学 阶段(地层学) 比例危险模型 胃肠病学 结直肠癌 癌症 C反应蛋白 炎症 生物 古生物学
作者
James H. Park,David G. Watt,Campbell S. Roxburgh,Paul G. Horgan,Donald C. McMillan
出处
期刊:Annals of Surgery [Lippincott Williams & Wilkins]
卷期号:263 (2): 326-336 被引量:168
标识
DOI:10.1097/sla.0000000000001122
摘要

Objective: This study aims to examine the clinical utility of the combination of TNM stage and modified Glasgow Prognostic Score (mGPS) in patients undergoing potentially curative resection of colorectal cancer (CRC). Background: Of measures of the systemic inflammatory response, the mGPS has been most extensively validated in patients with cancer. Methods: Data from 1000 consecutive patients undergoing potentially curative CRC resection from a single institution (January 1997–May 2013) were included. The relationship between mGPS [0–C-reactive protein (CRP) ≤ 10 mg/L, 1—CRP > 10 mg/L and albumin ≥35 g/L, 2—CRP > 10 mg/L and albumin < 35 g/L], TNM stage, and cancer-specific survival (CSS) and overall survival (OS) was examined using Kaplan-Meier log-rank survival analysis and multivariate Cox regression analysis. Results: An mGPS of 0, 1, and 2 was observed in 63%, 21%, and 16% of patients, respectively. Median follow-up was 56 months (interquartile range: 28–107 months). TNM and mGPS were independently associated with CSS and OS (all P < 0.001). In all patients, TNM and mGPS stratified 5-year CSS and OS from 97% and 87% (stage I, mGPS = 0) to 32% and 26% (stage III, mGPS = 2), respectively. In patients undergoing elective resection of colon cancer (n = 575), 5-year CSS and OS ranged from 100% and 87% (stage I, mGPS = 0) to 37% and 30% (stage III, mGPS = 2), respectively. Conclusions: This study shows how the combination of TNM and mGPS effectively stratifies outcome in patients undergoing potentially curative resection of CRC. These data support routine staging of both the tumor and the host in patients with CRC.
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