Chronic Inflammation Index-Based Tumor Subsite Classification Correlated with Chemotherapy Benefit and Survival Outcomes in Stage II-III Colorectal Cancer.

IF 4.2 2区 医学 Q2 IMMUNOLOGY
Journal of Inflammation Research Pub Date : 2025-05-26 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S517378
Ying Lu, Qiu-Ying Ye, Ou Mei, Ya-Nan Li, Yue Peng, Hou-Qun Ying, Xue-Xin Cheng
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引用次数: 0

Abstract

Purpose: This study aimed to develop and validate an integrated inflammatory prognostic index and to investigate associations between primary tumor location, chronic inflammatory status, adjuvant chemotherapy response, and survival outcomes in stage II-III colorectal cancer (CRC).

Patients and methods: A total of 1413 stage II-III CRC patients who underwent radical resection were enrolled and divided into discovery and validation cohorts. Preoperative systemic inflammatory biomarkers were quantified, and patients were followed for 3 years to establish an optimal chronic inflammatory index (CII) and evaluate its association with survival and chemotherapy efficacy across primary tumor locations.

Results: The comprehensive CII was the top-performing prognostic biomarker, with time-dependent AUCs of 0.71(95% CI: 0.68-0.74) for 36-month RFS and 0.74(95% CI: 0.70-0.77) for OS. Furthermore, the 3C (CII, CEA and CA19-9) combined score demonstrated prognostic predictive AUCs of 0.74(95% CI: 0.71-0.77) for RFS and 0.76(95% CI: 0.72-0.79) for OS in the overall population. The splenic flexure and ascending colon showed significantly elevated CII levels versus other subsites, and the disease was divided into the proximal colon, transverse colon, distal colon and rectum. A significant CII gradient emerged across subsites (proximal > transverse > distal > rectal), with corresponding survival decrements (log-rank p < 0.001). Proximal CRC exhibited marked worse survival outcomes (p = 0.002 for RFS and p = 0.001 for OS) and inferior chemotherapy efficacy (p < 0.001 for RFS and OS) versus rectal cancer, with no significant differences between adjacent subsites (all p > 0.05).

Conclusion: The validated CII represents a biologically relevant, subsite-specific prognostic biomarker in CRC. The chronic inflammation-based tumor subsite classification correlated with chemotherapy efficacy and clinical outcomes, highlighting its potential for personalized treatment strategies.

基于慢性炎症指数的肿瘤亚位分类与II-III期结直肠癌化疗获益和生存结局相关
目的:本研究旨在建立和验证一种综合炎症预后指标,并探讨II-III期结直肠癌(CRC)原发肿瘤位置、慢性炎症状态、辅助化疗反应和生存结果之间的关系。患者和方法:共纳入1413例接受根治性切除术的II-III期CRC患者,分为发现组和验证组。对术前全身炎症生物标志物进行量化,并对患者进行3年随访,以建立最佳慢性炎症指数(CII),并评估其与原发肿瘤部位的生存和化疗疗效的关系。结果:综合CII是表现最好的预后生物标志物,36个月RFS的时间依赖auc为0.71(95% CI: 0.68-0.74), OS的时间依赖auc为0.74(95% CI: 0.70-0.77)。此外,3C (CII, CEA和CA19-9)综合评分显示,在总体人群中,RFS的预后预测auc为0.74(95% CI: 0.71-0.77), OS的预后预测auc为0.76(95% CI: 0.72-0.79)。脾屈曲和升结肠的CII水平较其他亚位明显升高,病变分为近端结肠、横结肠、远端结肠和直肠。显著的CII梯度出现在亚位点(近端>横>远端>直肠),相应的生存降低(log-rank p < 0.001)。与直肠癌相比,近端结直肠癌表现出明显较差的生存结果(RFS组p = 0.002, OS组p = 0.001)和较差的化疗疗效(RFS和OS组p < 0.001),邻近亚位点之间无显著差异(均p < 0.05)。结论:经过验证的CII代表了CRC中具有生物学相关性、亚位特异性的预后生物标志物。基于慢性炎症的肿瘤亚位点分类与化疗疗效和临床结果相关,突出了其个性化治疗策略的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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