Faculty of Medicine Department of Medical Oncology, Ankara University, Cebeci, 06590, Ankara, Turkey.
Ankara University Cancer Research Institute, Ankara, Turkey.
J Cancer Res Clin Oncol. 2022 Dec;148(12):3537-3546. doi: 10.1007/s00432-022-04055-5. Epub 2022 May 26.
Pan-immune-inflammation value (PIV) is an easily accessible immune marker based on peripheral blood to estimate prognosis in patients with cancer. This study evaluates the prognostic value of PIV in patients with metastatic renal cell carcinoma (mRCC) treated with nivolumab.
In this retrospective cohort study, patients with mRCC treated with nivolumab in the second line and beyond were selected from the Turkish Oncology Group Kidney Cancer Consortium (TKCC) database. PIV was calculated using the following formula: neutrophil (10/mm) x monocyte (10/mm) x platelet (10/mm)/lymphocyte (10/mm).
A total of 152 patients with mRCC were included in this study. According to cut-off value for PIV, 77 (50.7%) and 75 (49.3%) patients fell into PIV-low ([Formula: see text] 372) and PIV-high (> 372) groups, respectively. In multivariate analysis, PIV-high (HR: 1.64, 95% CI 1.04-2.58, p = 0.033 for overall survival (OS); HR: 1.55, 95% CI 1.02-2.38, p = 0.042 for progression-free survival (PFS)) was independent risk factor for OS and PFS after adjusting for confounding variables, such as performance score, the International mRCC Database Consortium (IMDC) risk score, and liver metastasis.
This study established that pre-treatment PIV might be a prognostic biomarker in patients with mRCC treated with nivolumab in the second line and beyond.
Pan-immune-inflammation 值(PIV)是一种基于外周血的易于获取的免疫标志物,可用于评估癌症患者的预后。本研究评估了 PIV 在接受纳武利尤单抗二线及以上治疗的转移性肾细胞癌(mRCC)患者中的预后价值。
在这项回顾性队列研究中,从土耳其肿瘤学组肾癌联盟(TKCC)数据库中选择了接受纳武利尤单抗二线及以上治疗的 mRCC 患者。使用以下公式计算 PIV:中性粒细胞(10/mm)x 单核细胞(10/mm)x 血小板(10/mm)/淋巴细胞(10/mm)。
本研究共纳入 152 例 mRCC 患者。根据 PIV 的截断值,77 例(50.7%)和 75 例(49.3%)患者分别归入 PIV 低([公式:见正文] 372)和 PIV 高(>372)组。多变量分析显示,PIV 高(HR:1.64,95%CI 1.04-2.58,p=0.033,用于总生存期(OS);HR:1.55,95%CI 1.02-2.38,p=0.042,用于无进展生存期(PFS))是调整混杂变量(如表现评分、国际 mRCC 数据库联盟(IMDC)风险评分和肝转移)后 OS 和 PFS 的独立危险因素。
本研究表明,治疗前 PIV 可能是接受纳武利尤单抗二线及以上治疗的 mRCC 患者的预后生物标志物。