头颈部鳞状细胞癌患者的 PIV(泛免疫炎症值)预后能力。

Aina Sansa , Cristina Valero , Albert Pujol , Blanca Sauter , Julia Gayà , Miquel Quer , Xavier León
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引用次数: 0

摘要

简介泛免疫炎症值(PIV)是由以下比率得出的指数:(中性粒细胞×单核细胞×血小板)/淋巴细胞,已被提出作为不同肿瘤模型的预后生物标志物。本研究旨在分析PIV在头颈部鳞状细胞癌(HNSCC)患者中的预后能力:回顾性研究:2000-2017年间在本中心接受治疗的1 187例HNSCC患者。PIV值来自治疗开始前3周内进行的分析:PIV值与毒性消耗(0.001)、肿瘤位置(0.0001)、肿瘤扩展(0.0001)和组织学分级(0.016)明显相关。通过递归分区分析,根据 PIV 值定义了四个类别:类别 I:PIV 1,141.2 (n = 118,9.9%)。随着 PIV 类别的增加,疾病特异性生存率出现了明显的有序下降。生存率的下降与治疗类型、肿瘤扩展或原发肿瘤位置无关。在一项多变量研究中,PIV类别是疾病特异性生存率的独立预后因素:结论:PIV是HNSCC患者的预后生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic capacity of PIV (pan-immune-inflammation value) in patients with head and neck squamous cell carcinoma

Introduction

The pan-immune-inflammation value (PIV), an index that results from the following ratio: (neutrophils × monocytes × platelets)/lymphocytes, has been proposed as a prognostic biomarker in different tumour models. The aim of this study is to analyse the prognostic capacity of PIV in patients with head and neck squamous cell carcinoma (HNSCC).

Patients and methods

Retrospective study of 1187 patients with HNSCC treated at our centre between 2000−2017. PIV value was obtained from an analysis performed within 3 weeks prior to the start of treatment.

Results

PIV value was significantly associated with toxic consumption (0.001), tumour location (0.0001), tumour extension (0.0001), and histological grade (0.016). Four categories were defined based on PIV value using a recursive partitioning analysis: category I: PIV < 136.3 (n = 118, 9.9%), category II: PIV 136.3–451.1 (n = 594, 50.0%), category III: PIV 451.1−1,141.2 (n = 357, 30.1%), and category IV: PIV > 1141.2 (n = 118, 9.9%). A significant and ordered decrease in disease-specific survival was observed as the PIV category increased. This decrease in survival was independent of the type of treatment, tumour extension, or location of the primary tumour. The PIV category was and independent prognostic factor of disease-specific survival in a multivariable study.

Conclusions

PIV is a prognostic biomarker in patients with HNSCC.

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