Martin Daniel, Rödel Franz, Winkelmann Ria, Balermpas Panagiotis, Rödel Claus, Fokas Emmanouil
Department of Radiotherapy and Oncology, Goethe University Frankfurt, Frankfurt, Germany.
German Cancer Research Center (DKFZ), Heidelberg, Germany.
Front Immunol. 2017 Sep 29;8:1225. doi: 10.3389/fimmu.2017.01225. eCollection 2017.
Peripheral blood leukocytosis has been implicated in promoting tumor progression leading to worse survival, but the mechanisms behind this phenomenon remain unexplored. Here, we examined the prognostic role of pretreatment white blood cell (WBC) count and clinicopathologic parameters in the context of CD8+ tumor-infiltrating lymphocytes (TIL) and myeloperoxidase+ tumor-associated neutrophils (TANs) in patients with anal squamous cell carcinoma (ASCC) treated with definitive chemoradiotherapy (CRT). After a median follow-up of 26 months, leukocytosis correlated with advanced T-stage ( < 0.001) and N-stage ( < 0.001), and predicted for worse distant-metastasis-free survival ( = 0.006), disease-free-survival (DFS, = 0.029), and overall survival ( = 0.013). Importantly, leukocytosis was associated with a lower intraepithelial CD8+ TIL density ( = 0.014), whereas low CD8+ TIL expression in the intraepithelial compartment was associated with worse DFS ( = 0.028). Additionally, high TAN expression in the peritumoral compartment was associated with a significantly lower density of CD8+ TIL ( = 0.039), albeit, TAN expression lacked prognostic value. In conclusion, leukocytosis constitutes an important prognostic marker in ASCC patients treated with CRT. In conjunction with intratumoral TIL and TAN, these data provide for the first time important insight on the correlation of peripheral blood leukocytosis with the intratumoral immune contexture and could be relevant for future patient stratification using immunotherapies in ASCC.
外周血白细胞增多症被认为与肿瘤进展有关,会导致生存率降低,但这一现象背后的机制仍未得到探索。在此,我们研究了在接受根治性放化疗(CRT)的肛管鳞状细胞癌(ASCC)患者中,治疗前白细胞(WBC)计数及临床病理参数在CD8 +肿瘤浸润淋巴细胞(TIL)和髓过氧化物酶+肿瘤相关中性粒细胞(TAN)背景下的预后作用。经过26个月的中位随访,白细胞增多症与晚期T分期(<0.001)和N分期(<0.001)相关,并预测远处无转移生存期较差(=0.006)、无病生存期(DFS,=0.029)和总生存期(=0.013)。重要的是,白细胞增多症与上皮内CD8 + TIL密度较低相关(=0.014),而上皮内CD8 + TIL表达较低与较差的DFS相关(=0.028)。此外,瘤周区高TAN表达与CD8 + TIL密度显著降低相关(=0.039),尽管TAN表达缺乏预后价值。总之,白细胞增多症是接受CRT治疗的ASCC患者的重要预后标志物。结合肿瘤内TIL和TAN,这些数据首次提供了关于外周血白细胞增多症与肿瘤内免疫微环境相关性的重要见解,可能与未来ASCC患者使用免疫疗法进行分层有关。