Zhou Lin, Xu Le, Chen Lingli, Fu Qiang, Liu Zheng, Chang Yuan, Lin Zongming, Xu Jiejie
Department of Urology, Zhongshan Hospital, Fudan University, Shanghai, China.
Department of Urology, Ruijin Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Oncoimmunology. 2017 Feb 21;6(4):e1293211. doi: 10.1080/2162402X.2017.1293211. eCollection 2017.
Growing evidence shows tumor-infiltrating neutrophils (TINs) involvement in tumorigenesis. The objective of this study is to assess the prognostic effect of TINs and its impact on adjuvant chemotherapy benefits in muscle invasive bladder cancer (MIBC). A total of 142 MIBC patients from Zhongshan Hospital, 119 MIBC patients from FUSCC, and 405 MIBC patients from TCGA cohort were enrolled in the study. TINs were evaluated by immunohistochemical staining of CD66b or the CIBERSORT method. Patients with high TINs had a significantly poorer overall survival ( = 0.001, < 0.001, and = 0.002, respectively) in the three sets. In the multivariate analysis, the presence of high TINs (HR = 2.122, = 0.007; HR = 3.807, < 0.001; HR = 2.104, = 0.001; respectively) was identified as an independent prognostic factor for overall survival in the three sets. More importantly, Low TINs patients had significantly longer overall survival in patients without ACT in the three sets. Gene set enrichment analysis showed that lymphocyte activation ( < 0.001) and T cell activation ( = 0.008) were significantly enriched in the low TINs group. In addition, TINs were negatively correlated with CD8 T cells, suggesting that the status of high-TINs was linked to the status of immunosuppression in MIBC. TINs could be used as independent prognostic factor. Low TINs identified a subgroup of MIBC patients who appeared to benefit from adjuvant chemotherapy. Incorporation of TINs into TNM system could further stratify patients with different prognosis.
越来越多的证据表明肿瘤浸润性中性粒细胞(TINs)参与肿瘤发生。本研究的目的是评估TINs在肌肉浸润性膀胱癌(MIBC)中的预后作用及其对辅助化疗疗效的影响。本研究纳入了来自中山医院的142例MIBC患者、来自复旦大学附属肿瘤医院的119例MIBC患者以及来自TCGA队列的405例MIBC患者。通过CD66b免疫组化染色或CIBERSORT方法评估TINs。在这三组中,TINs水平高的患者总生存期明显更差(分别为P = 0.001、P < 0.001和P = 0.002)。在多变量分析中,高TINs的存在(HR分别为2.122,P = 0.007;HR为3.807,P < 0.001;HR为2.104,P = 0.001)被确定为这三组患者总生存期的独立预后因素。更重要的是,在这三组未接受辅助化疗(ACT)的患者中,TINs水平低的患者总生存期明显更长。基因集富集分析表明,淋巴细胞激活(P < 0.001)和T细胞激活(P = 0.008)在低TINs组中显著富集。此外,TINs与CD8 + T细胞呈负相关,表明高TINs状态与MIBC中的免疫抑制状态有关。TINs可作为独立的预后因素。低TINs确定了一组似乎能从辅助化疗中获益的MIBC患者亚组。将TINs纳入TNM系统可进一步对不同预后的患者进行分层。