Öztürk Yusuf, Kocabaş Muhammet, Karaköse Melia, Kulaksizoğlu Mustafa, Karakurt Feridun
Department of Endocrinology and Metabolism, Necmettin Erbakan University Faculty of Medicine, Konya, Türkiye.
Arch Endocrinol Metab. 2025 Apr 11;68:e240217. doi: 10.20945/2359-4292-2024-0217.
The pan-immune-inflammation value (PIV) is a novel inflammatory biomarker for evaluating inflammatory status in patients with cancer. The aim of this study was to evaluate the prognostic value of PIV in patients with differentiated thyroid cancers (DTCs).
The study included 376 patients with DTC who underwent curative resection. The PIV was calculated using the formula (neutrophils × monocytes × platelets)/lymphocytes. The TNM stages 3-4 were considered advanced. Patients were also categorized into low-, intermediate-, and high-risk groups according to the AmericanThyroid Association (ATA) risk classification system. Demographic, laboratory, and clinicopathological data were obtained from the patients' files. The predictive value of PIV on TNM advanced stage, ATA high-risk category, and distant metastases was evaluated using receiver operating characteristic (ROC) curve analysis.
The optimal PIV values for predicting TNM advanced stage, ATA high-risk category, and distant metastases were, respectively, 331.62 (area under the curve [AUC] 0.730, sensitivity 66.7%, specificity 64.8%), 365.52 (AUC 0.822, sensitivity 79.5%, specificity 76.9%), and 357.65 (AUC 0.774, sensitivity 75.2%, specificity 72%). On regression analysis, PIV ≥ 365.52 (odds ratio [OR] 29.150, 95% confidence interval [CI] 8.148-104.290, p < 0.001) and PIV ≥ 357.65 (OR 7.224, 95% CI 1.700-30.693, p = 0.007) emerged as independent risk factors for ATA high-risk category and distant metastases, respectively.
Among patients with DTC, PIV is an independent risk factor for distant metastases and ATA high-risk category. While this finding must be supported by more comprehensive studies, PIV has the potential to be used as a prognostic biomarker in these patients.
全免疫炎症值(PIV)是一种用于评估癌症患者炎症状态的新型炎症生物标志物。本研究旨在评估PIV在分化型甲状腺癌(DTC)患者中的预后价值。
本研究纳入了376例行根治性切除术的DTC患者。PIV采用公式(中性粒细胞×单核细胞×血小板)/淋巴细胞计算得出。TNM分期3 - 4期被视为晚期。患者还根据美国甲状腺协会(ATA)风险分类系统分为低、中、高风险组。从患者病历中获取人口统计学、实验室和临床病理数据。采用受试者工作特征(ROC)曲线分析评估PIV对TNM晚期、ATA高风险类别和远处转移的预测价值。
预测TNM晚期、ATA高风险类别和远处转移的最佳PIV值分别为331.62(曲线下面积[AUC] 0.730,敏感性66.7%,特异性64.8%)、365.52(AUC 0.822,敏感性79.5%,特异性76.9%)和357.65(AUC 0.774,敏感性75.2%,特异性72%)。回归分析显示,PIV≥365.52(比值比[OR] 29.150,95%置信区间[CI] 8.148 - 104.290,p < 0.001)和PIV≥357.65(OR 7.224,95% CI 1.700 - 30.693,p = 0.007)分别成为ATA高风险类别和远处转移的独立危险因素。
在DTC患者中,PIV是远处转移和ATA高风险类别的独立危险因素。虽然这一发现必须得到更全面研究的支持,但PIV有潜力作为这些患者的预后生物标志物。