从血液到结果:罗马尼亚三级医院直肠癌手术中的炎症生物标志物

IF 3 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Georgiana Viorica Moise, Catalin Vladut Ionut Feier, Vasile Gaborean, Alaviana Monique Faur, Vladut Iosif Rus, Calin Muntean
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引用次数: 0

摘要

背景:全身性炎症标志物已成为肿瘤风险分层的可获得和可重复的工具,但其在直肠癌中的预后价值仍不完全明确,特别是在急性手术环境中。本研究旨在评估6个基于炎症的指标——nlr、PLR、MLR、SII、SIRI和aisi——与直肠癌急诊和择期切除患者肿瘤分期、复发和预后的关系。方法:回顾性评估2018年至2024年期间接受治疗的174例患者。治疗前血液计数用于计算炎症指数。通过单因素和多因素分析,临床和病理参数与生物标志物水平相关。结果:在需要紧急手术的患者中,治疗前炎症标志物显著升高(例如,nlr: 3.34 vs. 2.4, p = 0.001;PLR: 204.1 vs. 137.8, p < 0.001;SII: 1008 vs. 693, p = 0.007),反映了先进的肿瘤生物学和免疫激活。值得注意的是,这些患者也有更高的IV期疾病(p = 0.029)和永久性造口(p = 0.002)的发生率。治疗后,复发与SII (p = 0.021)、AISI (p = 0.036)和PLR (p = 0.003)水平显著降低相关,这表明早期复发的潜在作用是免疫衰竭,而不是过度炎症。结论:炎症指标对直肠癌的肿瘤局部侵袭和宿主免疫状态提供了有价值的见解。将其纳入围手术期评估可以改善预后,特别是在急诊时。治疗后抑制这些标志物可以识别出尽管最初有治愈意图,但复发风险很高的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From Blood to Outcome: Inflammatory Biomarkers in Rectal Cancer Surgery at a Romanian Tertiary Hospital.

Background: Systemic inflammatory markers have emerged as accessible and reproducible tools for oncologic risk stratification, yet their prognostic value in rectal cancer remains incompletely defined, particularly in acute surgical settings. This study aimed to assess six inflammation-based indices-NLR, PLR, MLR, SII, SIRI, and AISI-in relation to tumor stage, recurrence, and outcomes among patients undergoing emergency versus elective resection for rectal cancer.

Methods: We retrospectively evaluated 174 patients treated between 2018 and 2024. Pre-treatment blood counts were used to calculate inflammatory indices. Clinical and pathological parameters were correlated with biomarker levels using univariate and multivariate analyses.

Results: Pre-treatment inflammation markers were significantly elevated in patients requiring emergency surgery (e.g.

, nlr: 3.34 vs. 2.4, p = 0.001; PLR: 204.1 vs. 137.8, p < 0.001; SII: 1008 vs. 693, p = 0.007), reflecting advanced tumor biology and immune activation. Notably, these patients also had higher rates of stage IV disease (p = 0.029) and permanent stoma (p = 0.002). Post-treatment, recurrence was paradoxically associated with significantly lower levels of SII (p = 0.021), AISI (p = 0.036), and PLR (p = 0.003), suggesting a potential role for immune exhaustion rather than hyperinflammation in early relapse.

Conclusions: Inflammatory indices provide valuable insights into both tumor local invasion and host immune status in rectal cancer. Their integration into perioperative assessment could improve prognostication, particularly in emergency presentations. Post-treatment suppression of these markers may identify patients at high risk for recurrence despite initial curative intent.

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