Hong Ying-Fen, Chen Zhan-Hong, Wei Li, Ma Xiao-Kun, Li Xing, Wen Jing-Yun, Wang Tian-Tian, Cai Xiu-Rong, Wu Dong-Hao, Chen Jie, Ruan Dan-Yun, Lin Ze-Xiao, Lin Qu, Dong Min, Wu Xiang-Yuan
Department of Medical Oncology and Guangdong Key Laboratory of Liver Disease, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Giangdong 510630, P.R. China.
Department of Medical Oncology of Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, Guangdong 510060, P.R. China.
Oncol Lett. 2017 Aug;14(2):2089-2096. doi: 10.3892/ol.2017.6420. Epub 2017 Jun 19.
The inflammatory microenvironment serves an important function in the progression of hepatocellular carcinoma (HCC). Peripheral blood lymphocyte-to-monocyte ratio (LMR), as a novel inflammatory biomarker combining an estimate of host immune homeostasis with the tumor microenvironment, has been identified to be a predictor of clinical outcomes in a number of malignancies. The present study aimed at investigating the prognostic value of LMR in patients with hepatitis B virus (HBV)-associated advanced HCC. A total of 174 patients with HBV-associated advanced HCC, without fever or signs of infections, were analyzed. Clinicopathological parameters, including LMR, were evaluated to identify predictors of overall survival time. Univariate and multivariate analysis was performed using Cox's proportional hazards model. A threshold value was determined using a time-dependent receiver operating characteristic curve. Univariate and multivariate analysis identified LMR as an independent prognostic factor in overall survival (OS) time in patients with HBV-associated advanced HCC (P<0.05). The threshold value of LMR was 2.22. All patients were divided into either a low LMR group (≤2.22) or a high LMR group (>2.22). The OS time of the high LMR group was significantly longer compared with the low LMR group (P<0.001). Patients in the high LMR group exhibited a significantly increased 3-month and 6-month OS rate, compared with that of the patients within the low LMR group (P<0.001). An increased level of LMR was significantly associated with the presence of metastasis, ascites and increased tumor size (P<0.01). LMR is an independent prognostic factor of HBV-associated advanced HCC patients and an increased baseline LMR level indicates an improved prognosis.
炎症微环境在肝细胞癌(HCC)进展中发挥着重要作用。外周血淋巴细胞与单核细胞比值(LMR)作为一种新型炎症生物标志物,将宿主免疫稳态评估与肿瘤微环境相结合,已被确定为多种恶性肿瘤临床结局的预测指标。本研究旨在探讨LMR在乙型肝炎病毒(HBV)相关晚期HCC患者中的预后价值。共分析了174例无发热或感染迹象的HBV相关晚期HCC患者。评估包括LMR在内的临床病理参数,以确定总生存时间的预测指标。使用Cox比例风险模型进行单因素和多因素分析。使用时间依赖性受试者工作特征曲线确定阈值。单因素和多因素分析确定LMR是HBV相关晚期HCC患者总生存(OS)时间的独立预后因素(P<0.05)。LMR的阈值为2.22。所有患者分为低LMR组(≤2.22)或高LMR组(>2.22)。高LMR组的OS时间明显长于低LMR组(P<0.001)。与低LMR组患者相比,高LMR组患者的3个月和6个月OS率显著提高(P<0.001)。LMR水平升高与转移、腹水和肿瘤大小增加显著相关(P<0.01)。LMR是HBV相关晚期HCC患者的独立预后因素,基线LMR水平升高表明预后改善。