Kırıkkale University, Department of Pathology, Kırıkkale, Turkey.
Pathol Oncol Res. 2020 Jul;26(3):1805-1816. doi: 10.1007/s12253-019-00758-2. Epub 2019 Nov 20.
Although local inflammatory response (LIR) is a reliable survival marker in colon cancers (CCs), there is no consensus on its use in daily practice. We investigated the prognostic value of LIR in a highly homogeneous population with a well-designed methodology.
Eighty stage-IIB CC patients operated between 2002 and 2012 were included in the study. Standardization was investigated for extra-biopsy evaluation methods (magnification, staining, and counting). Model A was used for intra-biopsy evaluation methods (block, section, and focus). So, this study makes important contributions to the standardization of pathological evaluations.
In method 1, the following analyzes showed more successful results for LIR: relationship with prognostic factors [tumour deposits (p=0.017), Crohn's-like reaction (p=0.019), advanced grade, (p=0.012), positive surgical margin (p=0.019), perineural invasion (p=0.025), mismatch repair proteins-proficiency (p=0.031)], reproducibility of the study (Kappa=0.49-0.73, Intra-class correlation=0.442-0.724), and correlation of estimates (r=0.704). The cut-off value was also quite useful (area of under ROC=0.820 [0.694-0.920]). In univariate analysis, low LIR was related to poor overall survival (OS; p<0.001) and poor relapse-free survival (RFS, p=0.001) . Multivariate analysis confirmed that low LIR is an independent poor survival marker for OS (Hazard Ratio [HR]=1.32 [1.08-1.61, p=0.005) and RFS (HR=1.50 [1.22-1.85], p<0.001).
Our results showed that low LIR had an independent prognostic significance in stage -IIB CCs. We also recommend using model A and method 1 for successful results and standardization.
尽管局部炎症反应(LIR)是结直肠癌(CC)可靠的生存标志物,但在日常实践中其应用尚未达成共识。我们采用设计良好的方法,在高度同质的人群中研究 LIR 的预后价值。
纳入 2002 年至 2012 年间接受手术的 80 例 IIB 期 CC 患者。研究中对额外活检评估方法(放大倍数、染色和计数)进行了标准化探索。模型 A 用于评估内活检方法(块、切片和焦点)。因此,本研究为病理评估的标准化做出了重要贡献。
在方法 1 中,以下分析显示 LIR 与预后因素的相关性更为成功:与肿瘤沉积物(p=0.017)、克罗恩样反应(p=0.019)、高级别(p=0.012)、阳性手术切缘(p=0.019)、神经周围侵犯(p=0.025)、错配修复蛋白-熟练程度(p=0.031),研究的可重复性(Kappa=0.49-0.73,组内相关系数=0.442-0.724),以及估计值的相关性(r=0.704)。临界值也非常有用(ROC 下面积=0.820[0.694-0.920])。在单因素分析中,低 LIR 与总生存(OS;p<0.001)和无复发生存(RFS,p=0.001)较差相关。多因素分析证实,低 LIR 是 OS(危险比[HR]=1.32[1.08-1.61,p=0.005]和 RFS(HR=1.50[1.22-1.85],p<0.001)的独立不良生存标志物。
我们的结果表明,低 LIR 在 IIB 期 CC 中具有独立的预后意义。我们还建议使用模型 A 和方法 1 以获得成功的结果和标准化。