Pan-immune-inflammation value as a prognostic biomarker for colon cancer and its variation by primary tumor location.

IF 4.3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY World Journal of Gastroenterology Pub Date : 2024-09-07 DOI:10.3748/wjg.v30.i33.3823
Qian-Yu Wang, Wen-Tao Zhong, Yi Xiao, Guo-Le Lin, Jun-Yang Lu, Lai Xu, Guan-Nan Zhang, Jun-Feng Du, Bin Wu
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Abstract

Background: A growing body of research indicates significant differences between left-sided colon cancers (LCC) and right-sided colon cancers (RCC). Pan-immune-inflammation value (PIV) is a systemic immune response marker that can predict the prognosis of patients with colon cancer. However, the specific distinction between PIV of LCC and RCC remains unclear.

Aim: To investigate the prognostic and clinical significance of PIV in LCC and RCC patients.

Methods: This multicenter retrospective cohort study included 1510 patients with colon cancer, comprising 801 with LCC and 709 with RCC. We used generalized lifting regression analysis to evaluate the relative impact of PIV on disease-free survival (DFS) in these patients. Kaplan-Meier analysis, as well as univariate and multivariate analyses, were used to examine the risk factors for DFS. The correlation between PIV and the clinical characteristics was statistically analyzed in these patients.

Results: A total of 1510 patients {872 female patients (58%); median age 63 years [interquartile ranges (IQR): 54-71]; patients with LCC 801 (53%); median follow-up 44.17 months (IQR 29.67-62.32)} were identified. PIV was significantly higher in patients with RCC [median (IQR): 214.34 (121.78-386.72) vs 175.87 (111.92-286.84), P < 0.001]. After propensity score matching, no difference in PIV was observed between patients with LCC and RCC [median (IQR): 182.42 (111.88-297.65) vs 189.45 (109.44-316.02); P = 0.987]. PIV thresholds for DFS were 227.84 in LCC and 145.99 in RCC. High PIV (> 227.84) was associated with worse DFS in LCC [PIV-high: Adjusted hazard ratio (aHR) = 2.39; 95% confidence interval: 1.70-3.38; P < 0.001] but not in RCC (PIV-high: aHR = 0.72; 95% confidence interval: 0.48-1.08; P = 0.114).

Conclusion: These findings suggest that PIV may predict recurrence in patients with LCC but not RCC, underscoring the importance of tumor location when using PIV as a colon cancer biomarker.

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作为结肠癌预后生物标志物的泛免疫炎症值及其随原发肿瘤位置的变化。
背景:越来越多的研究表明,左侧结肠癌(LCC)和右侧结肠癌(RCC)之间存在显著差异。泛免疫炎症值(PIV)是一种全身免疫反应标志物,可预测结肠癌患者的预后。目的:研究 PIV 在 LCC 和 RCC 患者中的预后和临床意义:这项多中心回顾性队列研究纳入了1510例结肠癌患者,其中801例为LCC患者,709例为RCC患者。我们采用广义提升回归分析来评估 PIV 对这些患者无病生存期(DFS)的相对影响。我们采用卡普兰-梅耶分析以及单变量和多变量分析来研究 DFS 的风险因素。对这些患者的 PIV 与临床特征之间的相关性进行了统计分析:共发现 1510 例患者{872 例女性患者(58%);中位年龄 63 岁[四分位数间距(IQR):54-71];LCC 患者 801 例(53%);中位随访时间 44.17 个月(IQR 29.67-62.32)}。RCC患者的PIV明显更高[中位数(IQR):214.34(121.78-386.72) vs 175.87(111.92-286.84),P <0.001]。经过倾向评分匹配后,LCC 和 RCC 患者的 PIV 无差异[中位数(IQR):182.42(111.88-297.65) vs 189.45(109.44-316.02);P = 0.987]。LCC和RCC的DFS PIV阈值分别为227.84和145.99。在 LCC 中,高 PIV(> 227.84)与较差的 DFS 相关[PIV-高:调整后危险比(aHR)= 2.39;95% 置信区间:1.70-3.38;P <0.001),但在 RCC 中却无关(PIV 高:aHR = 0.72;95% 置信区间:0.48-1.08;P = 0.114):这些研究结果表明,PIV可预测LCC患者的复发,但不能预测RCC患者的复发,这突出了将PIV作为结肠癌生物标记物时肿瘤位置的重要性。
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来源期刊
World Journal of Gastroenterology
World Journal of Gastroenterology 医学-胃肠肝病学
CiteScore
7.80
自引率
4.70%
发文量
464
审稿时长
2.4 months
期刊介绍: The primary aims of the WJG are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in gastroenterology and hepatology.
期刊最新文献
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