Deng Yu-Xiang, Lin Jun-Zhong, Peng Jian-Hong, Zhao Yu-Jie, Sui Qiao-Qi, Wu Xiao-Jun, Lu Zhen-Hai, Gao Yuan-Hong, Zeng Zhi-Fang, Pan Zhi-Zhong
Department of Colorectal Surgery.
Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine Guangzhou, Guangzhou, People's Republic of China.
Onco Targets Ther. 2017 Nov 22;10:5575-5583. doi: 10.2147/OTT.S146697. eCollection 2017.
Research indicates that cancer-triggered inflammation plays a pivotal role in carcinogenesis. Here, we aimed to evaluate the correlation of lymphocyte-to-monocyte ratio (LMR) before neoadjuvant chemoradiotherapy (CRT) with clinical outcomes in patients with locally advanced rectal cancer (LARC). We retrospectively enrolled 317 consecutive patients with LARC between 2004 and 2013. The optimal cutoff values of LMR were determined using receiver operating curve analysis. Overall survival (OS) and disease-free survival related to the LMR were analyzed using the log-rank test and multivariate Cox regression methods. We found that a low LMR (≤4.91) was prominently correlated with worse prognostic features and a shorter 3-year survival rate of LARC. Moreover, multivariate Cox analysis revealed that elevated LMR was an independent factor for better OS (hazard ratio 0.538, 95% confidence interval 0.292-0.991, =0.047). In addition, univariate logistic regression analysis showed that the LMR was not associated with tumor pathologic regression. In conclusion, LMR is identified as a valuable prognostic marker for predicting the OS of LARC patients receiving CRT.
研究表明,癌症引发的炎症在致癌过程中起关键作用。在此,我们旨在评估新辅助放化疗(CRT)前淋巴细胞与单核细胞比值(LMR)与局部晚期直肠癌(LARC)患者临床结局的相关性。我们回顾性纳入了2004年至2013年间连续的317例LARC患者。使用受试者工作特征曲线分析确定LMR的最佳截断值。采用对数秩检验和多因素Cox回归方法分析与LMR相关的总生存期(OS)和无病生存期。我们发现低LMR(≤4.91)与LARC较差的预后特征和较短的3年生存率显著相关。此外,多因素Cox分析显示,LMR升高是OS改善的独立因素(风险比0.538,95%置信区间0.292 - 0.991,P = 0.047)。此外,单因素逻辑回归分析表明,LMR与肿瘤病理退缩无关。总之,LMR被确定为预测接受CRT的LARC患者OS的有价值的预后标志物。