局部晚期直肠癌患者术前泛免疫炎症值的预测和预后价值。

0 MEDICINE, RESEARCH & EXPERIMENTAL
Peipei Shen, Yu Xu, Jiahao Zhu, Danqi Qian, Bo Yang, Yong Mao, Shengjun Ji, Ke Gu, Yutian Zhao
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引用次数: 0

摘要

本研究旨在探讨泛免疫炎症值(PIV)在接受新辅助化放疗(nCRT)后进行全直肠系膜切除术的局部晚期直肠癌(LARC)患者中的预后价值。我们回顾性地收集并分析了215例切除的LARC患者的临床病理数据。我们使用X-tile软件确定了PIV预测总生存期(OS)的最佳阈值。评估了PIV对病理完全缓解(pCR)、OS和无病生存(DFS)的预测能力,并与其他炎症标志物进行了比较。对 pCR 进行了单变量和多变量逻辑回归分析,对 OS 和 DFS 进行了 Cox 回归分析。根据X-tile软件,PIV的最佳阈值被确定为454.7。然后将患者分为低 PIV 组(≤ 454.7)和高 PIV 组(> 454.7),分别有 153 名和 62 名患者。与其他炎症指标相比,PIV对pCR、OS和DFS的预测能力更强。与高 PIV 患者相比,低 PIV LARC 患者的 pCR(P = 0.029)、OS(P = 0.002)和 DFS(P = 0.001)率明显更高。多变量回归分析发现,PIV 是 pCR(几率比 = 0.32;95% 置信区间 [CI],0.10-0.80;P = 0.014)、OS(危险比 = 3.08;95% CI,1.77-5.35;P = 0.001)和 DFS(危险比 = 2.53;95% CI,1.58-4.06;P = 0.002)的独立预后因素。这项研究证实,术前PIV可作为接受nCRT治疗的LARC患者的一个有用的独立预后因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictive and prognostic value of preoperative pan-immune-inflammation value in patients with locally advanced rectal cancer.

This study aimed to investigate the prognostic value of the pan-immune-inflammation value (PIV) in patients with locally advanced rectal cancer (LARC) who received neoadjuvant chemoradiotherapy (nCRT) followed by total mesorectal excision. We retrospectively collected and analyzed the clinicopathological data of 215 resected LARC patients. X-tile software was used to determine the optimal threshold value for PIV in predicting overall survival (OS). The predictive ability of PIV for pathological complete regression (pCR), OS, and disease-free survival (DFS) was evaluated and compared with other inflammation markers. Univariate and multivariate logistic regression analyses for pCR and Cox regression analyses for OS and DFS were conducted. The optimal threshold value for PIV was determined to be 454.7 based on the X-tile software. Patients were then categorized into low (≤ 454.7) and high (> 454.7) PIV groups comprising 153 and 62 patients, respectively. PIV demonstrated superior predictive ability for pCR, OS, and DFS compared to other inflammation markers. LARC patients with low PIV had significantly higher pCR (P = 0.029), OS (P = 0.002), and DFS (P = 0.001) rates compared to those with high PIV. Multivariate regression analysis identified PIV as an independent prognostic factor for pCR (odds ratio = 0.32; 95% confidence interval [CI], 0.10-0.80; P = 0.014), OS (hazard ratio = 3.08; 95% CI, 1.77-5.35; P = 0.001), and DFS (hazard ratio = 2.53; 95% CI, 1.58-4.06; P = 0.002). This study confirmed that preoperative PIV could serve as a useful independent prognostic factor in LARC patients treated with nCRT.

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